WO2018224439A1 - Nouveaux anticorps anti-hsa - Google Patents

Nouveaux anticorps anti-hsa Download PDF

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Publication number
WO2018224439A1
WO2018224439A1 PCT/EP2018/064622 EP2018064622W WO2018224439A1 WO 2018224439 A1 WO2018224439 A1 WO 2018224439A1 EP 2018064622 W EP2018064622 W EP 2018064622W WO 2018224439 A1 WO2018224439 A1 WO 2018224439A1
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Prior art keywords
antibody
functional fragment
seq
sequence
light chain
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PCT/EP2018/064622
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English (en)
Inventor
Tea Gunde
Sebastian Meyer
Christian Hess
Tessa BIERI
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Numab Innovation Ag
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Application filed by Numab Innovation Ag filed Critical Numab Innovation Ag
Priority to KR1020197035189A priority Critical patent/KR20200015505A/ko
Priority to CA3064160A priority patent/CA3064160A1/fr
Priority to JP2019566084A priority patent/JP7130678B2/ja
Priority to CN201880036722.9A priority patent/CN110709418B/zh
Priority to AU2018280679A priority patent/AU2018280679A1/en
Priority to IL271127A priority patent/IL271127B2/en
Priority to US16/618,864 priority patent/US11365240B2/en
Priority to EP18729642.1A priority patent/EP3634997A1/fr
Publication of WO2018224439A1 publication Critical patent/WO2018224439A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/24—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
    • C07K16/244—Interleukins [IL]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/31—Immunoglobulins specific features characterized by aspects of specificity or valency multispecific
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/33—Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
    • C07K2317/62—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
    • C07K2317/622—Single chain antibody (scFv)
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
    • C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
    • C07K2317/94—Stability, e.g. half-life, pH, temperature or enzyme-resistance

Definitions

  • the present invention relates to novel antibodies that are specific for human serum albumin (HSA).
  • HSA human serum albumin
  • This invention relates to a novel antibody with binding specificity for human serum albumin, which has advantageous properties, such as high stability, reduced aggregation propensity, and improved binding affinity, and which is particularly suitable for the generation of multispecific antibody constructs.
  • antibodies have become an increasingly important class of biomolecules for research, diagnostic and therapeutic purposes. Initially, antibodies were exclusively obtained by immunizing animals with the corresponding antigen of interest. While antibodies of non-human origin can be used in research and diagnostics, in therapeutic approaches the human body may recognize non-human antibodies as foreign and raise an immune response against the non-human antibody drug substance, rendering it less or not effective. Thus, recombinant methods have been set up to render non-human antibodies less immunogenic.
  • the resulting mAb or functional fragment ideally retains the desired pharmacodynamic properties of the donor mAb, while displaying drug-like biophysical properties and minimal immunogenicity.
  • the biophysical properties of functional fragments of antibodies With respect to the biophysical properties of functional fragments of antibodies, the shorter half-life in plasma, when compared to full IgG antibodies, has been a major concern for the developability of therapeutic molecules.
  • therapeutic proteins have been produced as a genetic fusion with a natural protein that has a long serum half-life; either 67 kDa serum albumin (SA) (Syed et al., 1997; Osborn et al., 2002) or the Fc portion of an antibody, which adds an additional 60-70 kDa in its natural dimeric form, depending on glycosylation (Mohler et al., 1993).
  • SA serum albumin
  • Fc portion of an antibody which adds an additional 60-70 kDa in its natural dimeric form, depending on glycosylation (Mohler et al., 1993).
  • any such antibody would have to exhibit a complex pattern of features in order to successfully address the open issues such an approach poses: (i) the anti-HSA antibody or fragment thereof would have to have a high affinity for HSA; (ii) the anti-HSA antibody or fragment thereof would have to have a high affinity at pH values of about 5.5 and about 7.4 in order to safeguard stable binding at the physiologically relevant conditions; (iii) the antibody has to be specific for HSA, but offer cross-reactivity to non-human primate and/or rodent serum albumin in order to enable the performance of appropriate pre-clinical testing of constructs comprising such anti-HSA antibody or fragment thereof; (iv) binding of the anti-HSA antibody or fragment thereof to HSA has to preserve the ability of the antibody-bound HSA to bind FcRn to allow the anti-HSA antibody or fragment thereof to be recycled with HSA through the interaction between HSA and FcRn; (v) when used in an
  • the present invention relates to novel antibodies that are specific for human serum albumin (HSA).
  • HSA human serum albumin
  • the present invention relates to an antibody or functional fragment thereof which is specific for human serum albumin, comprising: a variable light chain, wherein the variable light chain comprises, from N-terminus to C-terminus, the regions LFW1 -LCDR1 -LFW2-LCDR2-LFW3-LCDR3-LFW4, wherein each LFW designates a light chain framework region, and each LCDR designates a light chain complementarity-determining region, and wherein said LCDRs together exhibit at least 90% sequence identity to the corresponding LCDRs taken from a VL sequence according to SEQ ID NO: 1 or SEQ ID NO: 3;
  • variable heavy chain wherein the variable light chain comprises, from N-terminus to C-terminus, the regions HFW1 -HCDR1 -HFW2-HCDR2-HFW3-HCDR3-HFW4, wherein each HFW designates a heavy chain framework region, and each HCDR designates a heavy chain complementarity-determining region, and wherein said HCDRs together exhibit at least 90% sequence identity to the corresponding HCDRs taken from a VH sequence according to SEQ ID NO: 2 or SEQ ID NO: 4.
  • the present invention relates to a pharmaceutical composition
  • a pharmaceutical composition comprising the antibody or functional fragment thereof of the present invention, and optionally a pharmaceutically acceptable carrier and/or excipient.
  • the present invention relates to a nucleic acid sequence or a collection of nucleic acid sequences encoding the antibody or functional fragment thereof of the present invention.
  • the present invention relates to a vector or a collection of vectors comprising the nucleic acid sequence or the collection of nucleic acid sequences of the present invention.
  • the present invention relates to a host cell, particularly an expression host cell, comprising the nucleic acid sequence or the collection of nucleic acid sequences of the present invention, or the vector or collection of vectors of the present invention.
  • the present invention relates to a method for producing the antibody or functional fragment thereof of the present invention, comprising the step of expressing the nucleic acid sequence or the collection of nucleic acid sequences of the present invention, or the vector or collection of vectors of the present invention, or the host cell, particularly the expression host cell, of the present invention.
  • the present invention relates to a method of generating a multispecific construct, comprising the step of cloning, in one or more steps, one or more nucleic acid sequences encoding the antibody or functional fragment thereof according to the present invention, into a multispecific construct comprising at least a second bioactive domain, and, optionally, one or more additional bioactive domains.
  • the present invention relates to a multispecific polypeptide construct comprising (i) an antibody or functional fragment thereof according to any one of claims 1 to 4; and (ii) a second bioactive domain; and, optionally, (iii) one or more additional bioactive domains.
  • the present invention relates to the antibody or functional fragment thereof of the present invention, or to a multispecific polypeptide construct comprising the antibody or functional fragment thereof of the present invention for use as a medicament.
  • the present invention relates to the use of the antibody or functional fragment thereof of the present invention, or a multispecific polypeptide construct comprising the antibody or functional fragment thereof of the present invention in the manufacture of a medicament.
  • the present invention relates to a method of treating a subject suffering from a disease, particularly a human disease, comprising administering to said subject an effective amount of the antibody or functional fragment thereof of the present invention or a multispecific polypeptide construct comprising the antibody or functional fragment thereof of the present invention.
  • the present invention relates to use of the antibody or functional fragment thereof of the present invention, or to a multispecific polypeptide construct comprising the antibody or functional fragment thereof of the present invention in the treatment of a disease, particularly a human disease.
  • Figure 1 shows pharmacodynamic parameters of PR0462 following intravenous administration (3 mg/ml) to cynomolgus monkeys (3 per group, average shown; data see Table 8, Example 7). Blood samples were taken over a period of 21 days. The graph shows the mean group plasma concentrations of PR0462. Later time points are omitted because of the development of anti-drug antibodies.
  • Figure 2 shows the results of the mouse PK study discussed in Example 6 (mean group plasma concentrations of PR0497 in male CD-1 mice intravenously dosed with 5 mg/kg of test article; data see Table 9).
  • Figure 3 shows the structure of the multispecific construct PR0497.
  • HSA human serum albumin
  • HSA Human Serum Albumin
  • P02768 Human Serum Albumin
  • Multifunctional HSA protein is associated with a structure that allowed to bind and transport a number of metabolites such as fatty acids, metal ions, bilirubin and some drugs (Fanali, Molecular Aspects of Medicine, Vol. 33, 2012, 209-290).
  • HSA concentration in serum is around 3.5-5 g/dL.
  • Albumin-binding antibodies and fragments thereof may be used, for example, for extending the in vivo serum half-life of drugs or proteins conjugated thereto.
  • the present invention relates to an antibody or functional fragment thereof which is specific for human serum albumin, comprising: a variable light chain, wherein the variable light chain comprises, from N-terminus to C-terminus, the regions LFW1 -LCDR1 -LFW2-LCDR2-LFW3-LCDR3-LFW4, wherein each LFW designates a light chain framework region, and each LCDR designates a light chain complementarity-determining region, and wherein said LCDRs together exhibit at least 90% sequence identity to the corresponding LCDRs taken from a VL sequence according to SEQ ID NO: 1 or SEQ ID NO: 3;
  • variable heavy chain wherein the variable light chain comprises, from N-terminus to C-terminus, the regions HFW1 -HCDR1 -HFW2-HCDR2-HFW3-HCDR3-HFW4, wherein each HFW designates a heavy chain framework region, and each HCDR designates a heavy chain complementarity-determining region, and wherein said HCDRs together exhibit at least 90% sequence identity to the corresponding HCDRs taken from a VH sequence according to SEQ ID NO: 2 or SEQ ID NO: 4.
  • the term “antibody” is used as a synonym for "immunoglobulin” (Ig), which is defined as a protein belonging to the class IgG, IgM, IgE, IgA, IgY or IgD (or any subclass thereof), and includes all conventionally known antibodies.
  • Ig immunoglobulin
  • a naturally occurring “antibody” is a glycoprotein comprising at least two heavy (H) chains and two light (L) chains inter-connected by disulfide bonds. Each heavy chain is comprised of a heavy chain variable region (abbreviated herein as VH) and a heavy chain constant region.
  • VH heavy chain variable region
  • the heavy chain constant region is comprised of three domains, CH1 , CH2 and CH3.
  • Each light chain is comprised of a light chain variable region (abbreviated herein as VL) and a light chain constant region.
  • the light chain constant region is comprised of one domain, CL.
  • the VH and VL regions can be further subdivided into regions of hypervariability, termed complementarity determining regions (CDRs), interspersed with regions that are more conserved, termed framework regions (FWs).
  • CDRs complementarity determining regions
  • FWs framework regions
  • Each VH and VL is composed of three CDRs and four FWs arranged from amino-terminus to carboxy- terminus in the following order: FW1 -CDR1 -FW2-CDR2-FW3-CDR3-FW4.
  • the variable regions of the heavy and light chains contain a binding domain that interacts with an antigen.
  • antibody fragment refers to at least one portion of an intact antibody, or recombinant variants thereof
  • functional fragment refers an antibody fragment comprising at least an antigen binding domain, e.g., an antigenic determining variable region of an intact antibody, that is sufficient to confer recognition and specific binding of the functional antibody fragment to a target, such as an antigen.
  • Examples of functional antibody fragments include, but are not limited to, Fab, Fab', F(ab')2, and Fv fragments, scFv antibody fragments, linear antibodies, single domain antibodies such as sdAb (either VL or VH), camelid VHH domains, and multi- specific molecules formed from antibody fragments such as a bivalent fragment comprising two or more, e.g., two, Fab fragments linked by a disulfide bridge at the hinge region, or two or more, e.g., two, isolated CDR or other epitope binding fragments of an antibody linked.
  • An antibody fragment can also be incorporated into single domain antibodies, maxibodies, minibodies, nanobodies, intrabodies, diabodies, triabodies, tetrabodies, v-NAR and bis-scFv (see, e.g., Hollinger and Hudson, Nature Biotechnology 23:1 126-1 136, 2005).
  • Antibody fragments can also be grafted into scaffolds based on polypeptides such as a fibronectin type III (Fn3) (see U.S. Patent No. : 6,703,199, which describes fibronectin polypeptide minibodies).
  • Fn3 fibronectin type III
  • an “antigen-binding region” or “antigen-binding domain” of an antibody typically is found in one or more hypervariable region(s) of an antibody, i.e., the CDR1 , CDR2, and/or CDR3 regions; however, the variable “framework” regions can also play an important role in antigen binding, such as by providing a scaffold for the CDRs.
  • the constant regions of the antibodies may mediate the binding of the immunoglobulin to host tissues or factors, including various cells of the immune system (e.g., effector cells) and the first component (Clq) of the classical complement system.
  • the term "antibody” includes for example, monoclonal antibodies, human antibodies, humanized antibodies, camelid antibodies, or chimeric antibodies.
  • the antibodies can be of any isotype (e.g., IgG, IgE, IgM, IgD, IgA and IgY), class (e.g., lgG1 , lgG2, lgG3, lgG4, lgA1 and lgA2) or subclass.
  • isotype e.g., IgG, IgE, IgM, IgD, IgA and IgY
  • class e.g., lgG1 , lgG2, lgG3, lgG4, lgA1 and lgA2
  • subclass e.g., lgG1 , lgG2, lgG3, lgG4, lgA1 and lgA2
  • CDRs Complementarity Determining Regions
  • IMGT Immunol., 27, 55-77 (2003)
  • VH heavy chain variable domain
  • HCDR2 50-65
  • HCDR3 95-102
  • LCDR3 24-34
  • LCDR1 light chain variable domain
  • LCDR2 89-97
  • the CDR amino acids in the VH are numbered 26-32 (HCDR1 ), 52-56 (HCDR2), and 95- 102 (HCDR3); and the amino acid residues in VL are numbered 24-34 (LCDR1 ), 50- 56 (LCDR2), and 89-97 (LCDR3).
  • the CDRs consist of amino acid residues 26-35 (HCDR1 ), 50-65 (HCDR2), and 95-102 (HCDR3) in human VH and amino acid residues 24-34 (LCDR1 ), 50-56 (LCDR2), and 89-97 (LCDR3) in human VL
  • the CDR amino acid residues in the VH are numbered approximately 26-35 (HCDR1 ), 51 -57 (HCDR2) and 93-102 (HCDR3)
  • the CDR amino acid residues in the VL are numbered approximately 27-32 (LCDR1 ), 50-52 (LCDR2), and 89-97 (LCDR3) (numbering according to "Kabat").
  • the CDRs of an antibody can be determined using the program IMGT/DomainGap Align.
  • CDRs LCDR1 (also referred to as CDR-L1 ): L24- L42; LCDR2 (also referred to as CDR-L2): L58-L72; LCDR3 (also referred to as CDR-L3): L107-L138; HCDR1 (also referred to as CDR-H1 ): H27-H42; HCDR2 (also referred to as CDR-H2): H57-H76; HCDR3 (also referred to as CDR-H3): H108- H138.
  • the "antigen-binding region” comprises at least amino acid residues 4 to 138 of the variable light (VL) chain and 5 to 138 of the variable heavy (VH) chain (in each case numbering according to Honegger & Pluckthun), more preferably amino acid residues 3 to 144 of VL and 4 to 144 of VH, and particularly preferred are the complete VL and VH chains (amino acid positions 1 to 149 of VL and 1 to 149 of VH).
  • the framework regions and CDRs are indicated in Table 7.
  • a preferred class of immunoglobulins for use in the present invention is IgG.
  • “Functional fragments” of the invention include the domain of a F(ab') 2 fragment, a Fab fragment, Fv and scFv.
  • the F(ab') 2 or Fab may be engineered to minimize or completely remove the intermolecular disulphide interactions that occur between the CH1 and CL domains.
  • the antibodies or functional fragments thereof of the present invention may be part of bi- or multifunctional constructs, as further described in Sections [0079] to [0082].
  • a binding molecule is "specific to/for”, “specifically recognizes”, or “specifically binds to” a target, such as for example human serum albumin, when such binding molecule is able to discriminate between such target biomolecule and one or more reference molecule(s), since binding specificity is not an absolute, but a relative property.
  • a target such as for example human serum albumin
  • binding specificity is not an absolute, but a relative property.
  • “specific binding” is referring to the ability of the binding molecule to discriminate between the target biomolecule of interest and an unrelated biomolecule, as determined, for example, in accordance with a specificity assay methods known in the art.
  • Such methods comprise, but are not limited to Western blots, ELISA, RIA, ECL, IRMA, SPR (Surface plasmon resonance) tests and peptide scans.
  • a standard ELISA assay can be carried out.
  • the scoring may be carried out by standard colour development ⁇ e.g. secondary antibody with horseradish peroxide and tetramethyl benzidine with hydrogen peroxide).
  • the reaction in certain wells is scored by the optical density, for example, at 450 nm.
  • an SPR assay can be carried out, wherein at least 10-fold, preferably at least 100-fold difference between a background and signal indicates on specific binding.
  • determination of binding specificity is performed by using not a single reference biomolecule, but a set of about three to five unrelated biomolecules, such as milk powder, transferrin or the like.
  • binding also may refer to the ability of a binding molecule to discriminate between the target biomolecule and one or more closely related biomolecule(s), which are used as reference points, such as, for example, serum albumins from a different species, e.g. bovine serum albumin. Additionally, “specific binding” may relate to the ability of a binding molecule to discriminate between different parts of its target antigen, e.g. different domains, regions or epitopes of the target biomolecule, or between one or more key amino acid residues or stretches of amino acid residues of the target biomolecule.
  • epitope refers to that part of a given target biomolecule that is required for specific binding between the target biomolecule and a binding molecule.
  • An epitope may be continuous, i.e. formed by adjacent structural elements present in the target biomolecule, or discontinuous, i.e. formed by structural elements that are at different positions in the primary sequence of the target biomolecule, such as in the amino acid sequence of a protein as target, but in close proximity in the three-dimensional structure, which the target biomolecule adopts, such as in the bodily fluid.
  • variable light chain is a VK1 light chain, and/or said variable heavy chain is a VH3 chain.
  • said variable light chain is a chimeric light chain, comprising VK framework regions I to I I I and a ⁇ framework region IV.
  • light chain is a chimeric light chain, comprising:
  • FW4 which is selected from (a) a human VA germ line sequence for FW4, particularly a VA germ line sequence selected from the SEQ I D NO: 6 and SEQ I D NO: 7, preferably SEQ I D NO: 7; and (b) a VA-based sequence, which has one or two mutations, particularly one mutation, compared to the closest human VA germ line sequence for FW4 comprising an amino acid sequence selected from the SEQ I D NO: 6 and SEQ I D NO: 7, preferably SEQ I D NO: 7.
  • VH variable heavy chain
  • VK variable heavy chain
  • VA variable heavy chain sequences
  • Methods for the determination of sequence homologies for example by using a homology search matrix such as BLOSUM (Henikoff, S. & Henikoff, J. G., Proc. Natl. Acad. Sci. USA 89 (1 992) 1 0915-1 091 9), and methods for the grouping of sequences according to homologies are well known to one of ordinary skill in the art.
  • BLOSUM Henikoff, S. & Henikoff, J. G., Proc. Natl. Acad. Sci. USA 89 (1 992) 1 0915-1 091 9
  • VH VK and VA different subfamilies can be identified, as shown, for example, in Knappik et al., J. Mol. Biol.
  • antibody VK chains, VA chains, and VH chains are the result of the random rearrangement of germline ⁇ chain V and J segments, germline A chain V and J segments, and heavy chain V, D and J segments, respectively.
  • To which subfamily a given antibody variable chain belongs is determined by the corresponding V segment, and in particular by the framework regions FW1 to FW3.
  • any VH sequence that is characterized in the present application by a particular set of framework regions HFW1 to HFW3 only may be combined with any HFW4 sequence, for example a HFW4 sequence taken from one of the heavy chain germline J segments, or a HFW4 sequence taken from a rearranged VH sequence.
  • the HFW4 sequence is WGQGTLVTVSS.
  • the antibody or functional fragment of the present invention is an isolated antibody or functional fragment thereof.
  • isolated antibody means a polypeptide or a protein thereof which, by virtue of its origin or manipulation : (i) is present in a host cell as the expression product of a portion of an expression vector, or (ii) is linked to a protein or other chemical moiety other than that to which it is linked in nature, or (iii) does not occur in nature.
  • isolated it is further meant a protein that is: (i) chemically synthesized; or (ii) expressed in a host cell and purified away from associated proteins, as by gel chromatography.
  • isolated antibody also refers to antibody that is substantially free of other antibodies having different antigenic specificities (e.g., an isolated antibody that specifically binds to human serum albumin is substantially free of antibodies that specifically bind antigens other than human serum albumin).
  • An isolated antibody that specifically binds human serum albumin may, however, have cross-reactivity to other antigens, such as serum albumin molecules from other species (e.g., non-human primate and/or rodent serum albumin).
  • an isolated antibody may be substantially free of other cellular material and/or chemicals.
  • Binding affinity refers to intrinsic binding affinity which reflects 1 :1 interaction between members of a binding pair, e.g., interaction of a single antibody binding domain and its antigen.
  • the affinity can generally be represented by the dissociation constant (K D ).
  • K D dissociation constant
  • the antibody of the invention or the functional fragment may have a K D of between 1 to 50,000 pM, 1 to 40,000 pM, 1 to 30,000 pM, 1 to 25,000 pM, 1 to 20,000 pM, 1 to 10,000 pM, 1 to 7,500 pM, 1 to 5,000 pM, 1 to 4,000 pM, 1 to 3,000 pM, 1 to 2,000 pM, 1 to 1 ,500 pM, 1 to 1 ,000 pM, preferably as measured by surface plasmon resonance; more particularly as determined by the method shown in Example 2.1 .
  • the antibody of the invention or the functional fragment thereof has a K D value for the binding to human serum albumin of less than 50 nM, particularly less than 3 nM, more particularly less than 1 nM, preferably as measured by surface plasmon resonance; more particularly as determined by the method shown in Example 2.1 .
  • the antibody of the invention or the functional fragment has such K D value for the binding to human serum albumin both at pH values of about 5.5 and at about 7.4.
  • the antibody of the invention or the functional fragment may have a KD value for the binding to non-human primate and/or rodent serum albumin of between 1 to 250,000 pM, 1 to 200,000 pM, 1 to 150,000 pM, 1 to 100,000 pM, 1 to 75,000 pM, 1 to 50,000 pM, 1 to 40,000 pM, 1 to 30,000 pM, 1 to 20,000 pM, 1 to 10,000 pM, 1 to 7,500 pM, 1 to 5,000 pM, preferably as measured by surface plasmon resonance; more particularly as determined by the method shown in Example 2.1 .
  • the antibody of the invention or the functional fragment has a K D value for the binding to non-human primate and/or rodent serum albumin of less than 250 nM, particularly less than 100 nM, more particularly less than 50 nM, in particular as measured by surface plasmon resonance; more particularly as determined by the method shown in Example 2.1 .
  • variable light chain exhibits at least 60, 70, 80, 90, 91 , 92, 93, 94, 95, 96, 97, 98 or 99 percent, preferably at least 90 percent, sequence identity to a VL sequence according to SEQ ID NO: 1 or SEQ ID NO: 3, and/or wherein said variable heavy chain is a VH3 chain exhibiting at least 60, 70, 80, 90, 91 , 92, 93, 94, 95, 96, 97, 98 or 99 percent, preferably at least 90 percent, sequence identity to a VH sequence according to SEQ ID NO: 2 or SEQ ID NO: 4.
  • sequence identity or “percentage of sequence identity”
  • sequence similarity or “percentage of sequence similarity”.
  • sequence identity is determined by calculating the maximum number of amino acid residues that are identical between two polypeptide sequences, wherein gaps and/or insertions may be factored in order to allow for the largest degree of sequence overlap. For example, two 100mer polypeptides that are fully identical have a sequence identity of 100%. When they differ by a single mutation, or when one polypeptide contains a deletion of one amino acid, the sequence identity is 99% (99 out of 100 positions being identical).
  • the "percentage of sequence identity” is calculated by comparing two optimally aligned sequences over the window of comparison, determining the number of positions at which the identical nucleic acid base (e.g., A, T, C, G, U or I) or amino acid residue occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the comparison window (i.e., the window size), and multiplying the result by 100 to yield the percentage of sequence identity.
  • the “sequence similarity” is the degree of resemblance between two sequences when they are compared. Where necessary or desired, optimal alignment of sequences for comparison can be conducted, for example, by the local homology algorithm of Smith and Waterman (Adv. Appl. Math.
  • amino acid refers to naturally occurring and synthetic amino acids, as well as amino acid analogs and amino acid mimetics that function in a manner similar to the naturally occurring amino acids.
  • Naturally occurring amino acids are those encoded by the genetic code, as well as those amino acids that are later modified, e.g., hydroxyproline, gamma-carboxyglutamate, and O-phosphoserine.
  • polypeptide and "protein” are used interchangeably herein to refer to a polymer of amino acid residues.
  • the terms apply to amino acid polymers in which one or more amino acid residue is an artificial chemical mimetic of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers and non-naturally occurring amino acid polymer. Unless otherwise indicated, a particular polypeptide sequence also implicitly encompasses conservatively modified variants thereof.
  • said antibody or functional fragment thereof comprises (i) a variable light chain exhibiting at least 60, 70, 80, 90, 91 , 92, 93, 94, 95, 96, 97, 98 or 99 percent, preferably at least 90 percent, sequence identity to the VL sequence according to SEQ ID NO: 1 , and a VH chain exhibiting at least 60, 70, 80, 90, 91 , 92, 93, 94, 95, 96, 97, 98 or 99 percent, preferably at least 90 percent, sequence identity to the VH sequence according to SEQ ID NO: 2, or (ii) a variable light chain exhibiting at least 60, 70, 80, 90, 91 , 92, 93, 94, 95, 96, 97, 98 or 99 percent, preferably at least 90 percent, sequence identity to the VL sequence according to SEQ ID NO: 3, and a VH chain exhibiting at least 60, 70, 80, 90, 91 , 92, 93, 94, 95, 96, 97
  • the present invention relates to an antibody or functional fragment thereof which is specific for human serum albumin, comprising: (i) a variable light chain exhibiting at least 60, 70, 80, 90, 91 , 92, 93, 94, 95, 96, 97, 98 or 99 percent, preferably at least 90 percent, sequence identity to the VL sequence according to SEQ ID NO: 1 , wherein said variable light chain comprises CDR domains CDR1 , CDR2 and CDR3 taken from a the VL sequence according to SEQ ID NO: 1 ; and (ii) a variable heavy chain exhibiting at least 60, 70, 80, 90, 91 , 92, 93,
  • variable heavy chain comprises CDR domains CDR1 , CDR2 and CDR3 taken from a the VH sequence according to SEQ ID NO: 2.
  • the present invention relates to an antibody or functional fragment thereof which is specific for human serum albumin, comprising: (i) a variable light chain exhibiting at least 60, 70, 80, 90, 91 , 92, 93, 94, 95, 96, 97, 98 or 99 percent, preferably at least 90 percent, sequence identity to the VL sequence according to SEQ ID NO: 1 , wherein said variable light chain comprises CDR domains CDR1 , CDR2 and CDR3 taken from a the VL sequence according to SEQ ID NO: 1 , and wherein said variable light chain comprises K50Q and A51 P (AHo numbering); and (ii) a variable heavy chain exhibiting at least 60, 70, 80, 90, 91 , 92, 93, 94, 95, 96, 97, 98 or 99 percent, preferably at least 90 percent, sequence identity to the VH sequence according to SEQ ID NO: 2, wherein said variable heavy chain comprises CDR domains CDR1 , CDR2 and
  • the present invention relates to an antibody or functional fragment thereof which is specific for human serum albumin, comprising (i) a variable light chain comprising the amino acid sequence according to SEQ ID NO: 1 or a conservatively modified variant thereof, and (ii) a variable heavy chain comprising the amino acid sequence according to SEQ ID NO: 2 or a conservatively modified variant thereof.
  • the present invention relates to an antibody or functional fragment thereof which is specific for human serum albumin, comprising (i) a variable light chain comprising the amino acid sequence according to SEQ ID NO: 1 , and (ii) a variable heavy chain comprising the amino acid sequence according to SEQ ID NO: 2.
  • the present invention relates to an antibody or functional fragment thereof which is specific for human serum albumin, comprising: (i) a variable light chain exhibiting at least 60, 70, 80, 90, 91 , 92, 93, 94, 95, 96, 97, 98 or 99 percent, preferably at least 90 percent, sequence identity to the VL sequence according to SEQ ID NO: 3, wherein said variable light chain comprises CDR domains CDR1 , CDR2 and CDR3 taken from the VL sequence according to SEQ ID NO: 3; and (ii) a variable heavy chain exhibiting at least 60, 70, 80, 90, 91 , 92, 93, 94, 95, 96, 97, 98 or 99 percent, preferably at least 90 percent, sequence identity to the VH sequence according to SEQ ID NO: 4, wherein said variable heavy chain comprises CDR domains CDR1 , CDR2 and CDR3 taken from the VH sequence according to SEQ ID NO: 4.
  • the present invention relates to an antibody or functional fragment thereof which is specific for human serum albumin, comprising: (i) a variable light chain exhibiting at least 60, 70, 80, 90, 91 , 92, 93, 94, 95, 96, 97, 98 or 99 percent, preferably at least 90 percent, sequence identity to the VL sequence according to SEQ ID NO: 3, wherein said variable light chain comprises CDR domains CDR1 , CDR2 and CDR3 taken from the VL sequence according to SEQ ID NO: 3, and wherein said variable light chain comprises I2V, Q3V, K50Q and A51 P (AHo numbering); and (ii) a variable heavy chain exhibiting at least 60, 70, 80, 90, 91 , 92, 93, 94, 95, 96, 97, 98 or 99 percent, preferably at least 90 percent, sequence identity to the VH sequence according to SEQ ID NO: 4, wherein said variable heavy chain comprises CDR domains CDR1 , CDR
  • the present invention relates to an antibody or functional fragment thereof which is specific for human serum albumin, comprising (i) a variable light chain comprising the amino acid sequence according to SEQ ID NO: 3 or a conservatively modified variant thereof, and (ii) a variable heavy chain comprising the amino acid sequence according to SEQ ID NO: 4 or a conservatively modified variant thereof.
  • the present invention relates to an antibody or functional fragment thereof which is specific for human serum albumin, comprising (i) a variable light chain comprising the amino acid sequence according to SEQ ID NO: 3, and (ii) a variable heavy chain comprising the amino acid sequence according to SEQ ID NO: 4.
  • nucleic acid sequences refer to those nucleic acids, which encode identical or essentially identical amino acid sequences, or, where the nucleic acid does not encode an amino acid sequence, to essentially identical sequences. Because of the degeneracy of the genetic code, a large number of functionally identical nucleic acids encode any given protein. For instance, the codons GCA, GCC, GCG and GCU all encode the amino acid alanine.
  • nucleic acid variations are "silent variations", which are one species of conservatively modified variations.
  • Every nucleic acid sequence herein which encodes a polypeptide also describes every possible silent variation of the nucleic acid.
  • each codon in a nucleic acid except AUG, which is ordinarily the only codon for methionine, and TGG, which is ordinarily the only codon for tryptophan
  • TGG which is ordinarily the only codon for tryptophan
  • “conservatively modified variants” or “conservative variants” include individual substitutions, deletions or additions to a polypeptide sequence, which result in the substitution of an amino acid with a chemically similar amino acid. Conservative substitution tables providing functionally similar amino acids are well known in the art. Such conservatively modified variants are in addition to and do not exclude polymorphic variants, interspecies homologs, and alleles of the invention.
  • the following eight groups contain amino acids that are conservative substitutions for one another: 1 ) Alanine (A), Glycine (G); 2) Aspartic acid (D), Glutamic acid (E); 3) Asparagine (N), Glutamine (Q); 4) Arginine (R), Lysine (K); 5) Isoleucine (I), Leucine (L), Methionine (M), Valine (V); 6) Phenylalanine (F), Tyrosine (Y), Tryptophan (W); 7) Serine (S), Threonine (T); and 8) Cysteine (C), Methionine (M) (see, e.g., Creighton, Proteins (1984)).
  • the term "conservative sequence modifications” are used to refer to amino acid modifications that do not significantly affect or alter the binding characteristics of the antibody containing the amino acid sequence.
  • the antibody of the invention or the functional fragment thereof is characterized by one or more of the following parameters:
  • binding of the anti-HSA antibody or fragment thereof to HSA has to preserve the ability of the antibody-bound HSA to bind FcRn to allow the anti-HSA antibody or fragment thereof to be recycled with HSA through the interaction between HSA and FcRn, as determined by the assay used in Example 2.2;
  • v it has an average midpoint of thermal unfolding temperature (Tm) exceeding at least 60°C, when expressed in the scDb (single chain diabody format) or scFv (single chain variable fragment format) antibody format, preferably when expressed in the scFv format, in particular as determined by differential scanning fluorimetry (DSF) as described earlier (Egan, et al., MAbs, 9(1 ) (2017), 68-84; Niesen, et al., Nature Protocols, 2(9) (2007) 2212-2221 ), in particular when samples are diluted in five phosphate-citrate buffers at pH values ranging from 3.5 to 7.5 and containing 0.15- 0.25 M NaCI, particularly 0.15 M NaCI.
  • DSF differential scanning fluorimetry
  • the midpoint of transition for the thermal unfolding of the scFv constructs is determined by Differential Scanning Fluorimetry using the fluorescence dye SYPRO® Orange (see Wong & Raleigh, Protein Science 25 (201 6) 1834-1840). Samples in relevant excipient conditions are prepared at a final protein concentration of 50 ⁇ g ml "1 by spiking in stock excipients that are prepared in relevant buffer. For a buffer scouting experiment samples are diluted in final scFv buffers with different pH values (pH 3.4, 4.4, 5.4, 6.4 and 7.2) containing a final concentration of 5x SYPRO ® Orange in a total volume of 100 ⁇ .
  • the scFv DSF reference is measured as internal control. Twenty- five microliters of prepared samples are added in triplicate to white-walled AB gene PCR plates. The assay is performed in a qPCR machine used as a thermal cycler, and the fluorescence emission is detected using the software's custom dye
  • the PCR plate containing the test samples is subjected to a temperature ramp from 25°C to 96°C in increments of 1 °C with 30 s pauses after each temperature increment.
  • the total assay time is about two hours.
  • the Tm is calculated by the software GraphPad Prism using a mathematical second derivative method to calculate the inflection point of the curve; the reported Tm is an average of three measurements; in a particular embodiment, the determination of Tm is performed as described in Example 4.1 , wherein a sample is diluted in phosphate- citrate buffer at a pH value of 6.4, which contains 0.25 M NaCI; and
  • the fragment when used in an antibody fragment format, the fragment has to be stable as evidenced by the absence of, or limited amount of, degradation products and/or aggregates, as evidenced by less than 3% loss of monomeric content at 37°C during 28 days in a stress stability study, in particular performed in accordance with
  • Example 4.2 particularly less than 2% loss of monomeric content, in particular when the antibody of the invention is at a starting concentration of 10 mg/ml.
  • said antibody or functional fragment thereof has an average midpoint of thermal unfolding temperature (Tm) exceeding at least 65°C, preferably at least 69°C.
  • Tm thermal unfolding temperature
  • the protein is analyzed over the course of 14 days of storage at 37°C in 50 mM citrate-phosphate pH 6.4, 150 mM NaCI with respect to oligomerization by SE-HPLC. Prior to the study the samples are concentrated to 10 g 1-1 and dO time points are determined. The monomer content is quantified by separation of the samples on a Shodex KW-402.5-4F column and evaluation of the resulting chromatograms.
  • the area of the monomeric peak is divided by the total area of peaks that cannot be attributed to the sample matrix.
  • said antibody or functional fragment thereof exhibits a loss of monomeric content of less than 15%, 12%, 10%, 7%, 5%, or 2% when stored for two weeks at a concentration of 10 g/l at 37°C in 50 mM Citrate-Phosphate pH 6.4, 150 mM NaCI, preferably less than 5%, more preferably less than 2%.
  • the isolated antibody or functional fragment thereof is selected from: an IgG antibody, a Fab and an scFv fragment.
  • the antibody of the invention or functional fragment thereof is scFv antibody fragment.
  • Single-chain Fv" or “scFv” or “sFv” antibody fragments comprise the VH and VL domains of an antibody, wherein these domains are present in a single polypeptide chain.
  • the Fv polypeptide further comprises a polypeptide linker between the VH and VL domains which enables the sFv to form the desired structure for target binding.
  • Single-chain Fv or “scFv” antibody fragments comprise the VH and VL domains of antibody, wherein these domains are present in a single polypeptide chain.
  • the scFv polypeptides further comprises a polypeptide linker between the VH and VL domains which enables the scFv to form the desired structure for antigen binding (see, for example, Pluckthun, The pharmacology of Monoclonal Antibodies, vol. 1 13, Rosenburg and Moore eds., Springer- Verlag, New York, 1994, pp. 269-315).
  • said functional fragment is an scFv format comprising the linker according to SEQ ID NO: 5.
  • the isolated antibody or functional fragment thereof is a multispecific construct, e.g., bispecific construct, or a multivalent constructs, e.g., bivalent construct, which is an antibody format selected from any suitable multispecific, e.g.
  • bispecific, format known in the art including, by way of non-limiting example, formats based on a single-chain diabody (scDb), a tandem scDb (Tandab), a linear dimeric scDb (LD-scDb), a circular dimeric scDb (CD-scDb), a bispecific T-cell engager (BiTE; tandem di-scFv), a tandem tri-scFv, a tribody (Fab-(scFv)2) or bibody (Fab-(scFv)l ), triabody, scDb- scFv, bispecific Fab2, di-miniantibody, tetrabody, scFv-Fc-scFv fusion, di-diabody, DVD-lg, COVD, IgG-scFab, scFab-dsscFv, Fv2-Fc, IgG-scFv fusions, such as b
  • scDb single-chain diabody
  • scDb-scFv a scDb-scFv or MATCH, preferably scDb-scFv.
  • diabodies refers to antibody fragments with two antigen-binding sites, which fragments comprise a VH connected to VL in the same polypeptide chain (VH-VL). By using a linker that is too short to allow pairing between the two domains on the same chain, the domains are forced to pair with the complementary domains of another chain to create two antigen-binding sites.
  • Diabodies may be bivalent or bispecific. Diabodies are described more fully in, for example, EP404097, W01993/01 1 61 , Hudson et al., Nat. Med. 9:129-134 (2003), and Hollinger et al., Proc. Natl. Acad. Sci. USA 90: 6444-6448 (1993). Triabodies and tetrabodies are also described in Hudson et al., Nat. Med. 9:129-134 (2003).
  • the bispecific scDb in particular the bispecific monomeric scDb, particularly comprises two variable heavy chain domains (VH) or fragments thereof and two variable light chain domains (VL) or fragments thereof connected by linkers L1 , L2 and L3 in the order VHA-L1 -VLB-L2-VHB-L3-VLA, VHA-L1 -VHB-L2-VLB-L3-VLA, VLA-L1 -VLB-L2-VHB-L3-VHA, VLA-L1 -VHB-L2-VLB-L3-VHA, VHB-L1 -VLA-L2-VHA- L3-VLB, VHB-L1 -VHA-L2-VHA-L3-VLB, VHB-L1 -VHA-L2-VLA-L3-VLB, VLB-L1 -VLA-L2-VHA-L3-VHB or VLB-L1 - VHA-L2-VLA-L3-
  • the linker L1 particularly is a peptide of 2-10 amino acids, more particularly 3- 7 amino acids, and most particularly 5 amino acids
  • linker L3 particularly is a peptide of 1 -10 amino acids, more particularly 2-7 amino acids, and most particularly 5 amino acids
  • the middle linker L2 particularly is a peptide of 10-40 amino acids, more particularly 15-30 amino acids, and most particularly 20-25 amino acids.
  • the isolated antibody or functional fragment thereof is a multispecific and/or multivalent antibody in a MATCH format described in WO201 6/0202457; Egan T., et al., mAbs 9 (2017) 68-84.
  • the bispecific, bivalent, multispecific and/or multivalent constructs of the present invention can be produced using any convenient antibody manufacturing method known in the art (see, e.g., Fischer, N. & Leger, O., Pathobiology 74 (2007) 3-14 with regard to the production of bispecific constructs; Hornig, N. & Farber- Schwarz, A., Methods Mol. Biol. 907 (2012)713-727, and WO 99/57150 with regard to bispecific diabodies and tandem scFvs).
  • suitable methods for the preparation of the bispecific construct of the present invention further include, inter alia, the Genmab (see Labrijn et al., Proc. Natl. Acad. Sci.
  • These methods typically involve the generation of monoclonal antibodies, for example by means of fusing myeloma cells with the spleen cells from a mouse that has been immunized with the desired antigen using the hybridoma technology (see, e.g., Yokoyama et al., Curr. Protoc. Immunol. Chapter 2, Unit 2.5, 2006) or by means of recombinant antibody engineering (repertoire cloning or phage display/yeast display) (see, e.g., Chames & Baty, FEMS Microbiol. Letters 189 (2000) 1 -8), and the combination of the antigen-binding domains or fragments or parts thereof of two different monoclonal antibodies to give a bispecific construct using known molecular cloning techniques.
  • the present invention relates to a pharmaceutical composition
  • a pharmaceutical composition comprising the antibody or functional fragment thereof of the present invention, and optionally a pharmaceutically acceptable carrier and/or excipient.
  • phrases "pharmaceutically acceptable” refers to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings or animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.
  • compositions in accordance with the present disclosure may further routinely contain pharmaceutically acceptable concentrations of salt, buffering agents, preservatives, supplementary immune potentiating agents such as adjuvants and cytokines and optionally other therapeutic agents.
  • the composition may also include antioxidants and/or preservatives.
  • antioxidants may be mentioned thiol derivatives (e.g. thioglycerol, cysteine, acetylcysteine, cystine, dithioerythreitol, dithiothreitol, glutathione), tocopherols, butylated hydroxyanisole, butylated hydroxytoluene, sulfurous acid salts (e.g.
  • Suitable preservatives may for instance be phenol, chlorobutanol, benzylalcohol, methyl paraben, propyl paraben, benzalkonium chloride and cetylpyridinium chloride.
  • said antibodies or functional fragments thereof can be isolated, prepared, expressed, or created by recombinant means, such as antibodies expressed using a recombinant expression vector transfected into a host cell, antibodies isolated from a recombinant, combinatorial antibody library, or antibodies prepared, expressed, created or isolated by any other means that involves creation, e.g., via synthesis, genetic engineering of DNA sequences that encode human immunoglobulin sequences, or splicing of sequences that encode human immunoglobulins, e.g., human immunoglobulin gene sequences, to other such sequences.
  • recombinant means such as antibodies expressed using a recombinant expression vector transfected into a host cell, antibodies isolated from a recombinant, combinatorial antibody library, or antibodies prepared, expressed, created or isolated by any other means that involves creation, e.g., via synthesis, genetic engineering of DNA sequences that encode human immunoglobulin sequences, or splicing of sequences that encode human immunoglobulins,
  • the present invention relates to a nucleic acid sequence or a collection of nucleic acid sequences encoding the antibody or functional fragment thereof of the present invention.
  • nucleic acid is used herein interchangeably with the term “polynucleotide” and refers to deoxyribonucleotides or ribonucleotides and polymers thereof in either single- or double-stranded form.
  • the term encompasses nucleic acids containing known nucleotide analogs or modified backbone residues or linkages, which are synthetic, naturally occurring, and non-naturally occurring, which have similar binding properties as the reference nucleic acid, and which are metabolized in a manner similar to the reference nucleotides.
  • Examples of such analogs include, without limitation, phosphorothioates, phosphoramidates, methyl phosphonates, chiral-methyl phosphorates, 2-O-methyl ribonucleotides, peptide- nucleic acids (PNAs). Unless otherwise indicated, a particular nucleic acid sequence also implicitly encompasses conservatively modified variants thereof (e.g., degenerate codon substitutions) and complementary sequences, as well as the sequence explicitly indicated.
  • degenerate codon substitutions may be achieved by generating sequences in which the third position of one or more selected (or all) codons is substituted with mixed-base and/or deoxyinosine residues (Batzer et al., Nucleic Acid Res. 19:5081 , 1991 ; Ohtsuka et al., J. Biol. Chem. 260:2605-2608, 1985; and Rossolini et al., Mol. Cell. Probes 8:91 - 98, 1994).
  • the present invention relates to a vector or a collection of vectors comprising the nucleic acid sequence or a collection of nucleic acid sequences of the present invention.
  • vector or "expression vector” means a polynucleotide, most commonly a DNA plasmid, comprising nucleotide sequences encoding the antibodies of the invention or a fragment thereof for recombinant expression in host cells, preferably in mammalian cells.
  • a vector may, or may not, be able to replicate in a cell.
  • an expression vector can be transferred to a host cell by conventional techniques and the resulting cells can then be cultured by conventional techniques to produce an antibody described herein or a fragment thereof.
  • the present invention relates to a host cell, particularly an expression host cell, comprising the nucleic acid sequence or the collection of nucleic acid sequences of the present invention, or the vector or collection of vectors of the present invention.
  • a host cell contains a vector comprising a polynucleotide encoding both the variable heavy chain and variable light chain of the antibody of the invention, or a fragment thereof.
  • a host cell contains two different vectors, a first vector comprising a polynucleotide encoding a variable heavy chain of said antibody, or a fragment thereof, and a second vector comprising a polynucleotide encoding a variable light chain of said antibody, or a fragment thereof.
  • a first host cell comprises a first vector comprising a polynucleotide encoding a variable heavy chain of said antibody, or a fragment thereof
  • a second host cell comprises a second vector comprising a polynucleotide encoding a variable light chain of said antibody, or a functional fragment thereof.
  • the immunization of the rabbits or rodents may be performed with the antigen of interest as such, such as a protein, or, in the case of peptide or protein antigens, by DNA immunization of a rabbit with a nucleic acid, e.g. a plasmid, encoding the peptides or proteins of interest.
  • the antigen of interest such as a protein
  • a nucleic acid e.g. a plasmid
  • the present invention relates to a host cell, particularly an expression host cell, comprising the nucleic acid sequence or the collection of nucleic acid sequences of the present invention, or the vector or collection of vectors of the present invention.
  • host cell refers to a cell into which an expression vector has been introduced. It should be understood that such terms are intended to refer not only to the particular subject cell but to the progeny of such a cell. Because certain modifications may occur in succeeding generations due to either mutation or environmental influences, such progeny may not, in fact, be identical to the parent cell, but are still included within the scope of the term “host cell” as used herein.
  • the present invention relates to a method for producing the antibody or functional fragment thereof of the present invention, comprising the step of expressing the nucleic acid sequence or the collection of nucleic acid sequences of the present invention, or the vector or collection of vectors of the present invention, or the host cell, particularly the expression host cell, of the present invention.
  • the present invention relates to a method of generating a multispecific construct, comprising the step of cloning, in one or more steps, one or more nucleic acid sequences encoding the antibody or functional fragment thereof according to the present invention, into a multispecific construct comprising at least a second bioactive domain, and, optionally, one or more additional bioactive domains.
  • the present invention relates to a multispecific polypeptide construct comprising (i) an antibody or functional fragment thereof according to the present invention; and (ii) a second bioactive domain; and, optionally, (iii) one or more additional bioactive domains.
  • the second bioactive domain is a second antibody or functional fragment thereof.
  • At least one of said optional, additional bioactive domains is present, particularly wherein said additional bioactive domain is a third antibody or functional fragment thereof.
  • the multispecific polypeptide construct further comprises one or more polypeptide linkers.
  • said multispecific polypeptide is a monomeric polypeptide, particularly a monomeric polypeptide wherein the antibody or functional fragment thereof according to the present invention is an scFv antibody fragment linked via a linker to said second bioactive domain, particularly wherein said second bioactive domain is a second scFv antibody fragment.
  • said multispecific polypeptide is a dimeric polypeptide, particularly a dimeric polypeptide, wherein the association of the two polypeptides is caused by the association of complementary VL and VH domains of antibody fragments comprised in said multispecific polypeptide.
  • the multispecific polypeptide is a multispecific antibody construct in accordance with the teaching of WO 201 6/202457.
  • the multispecific polypeptide is a single-chain diabody construct (scDb).
  • the multispecific polypeptide is a Fab-scFv) n construct (n being an integer selected from 1 , 2, 3, or 4) that employs a heterodimeric assembly of a Fab fragment consisting of VL-CL and VH-CH1 with either constant domain forming a scaffold, to which one or more scFv fragments are attached via flexible linkers.
  • the present invention relates to the antibody or functional fragment thereof of the present invention, or to a multispecific polypeptide construct comprising the antibody or functional fragment thereof of the present invention for use as a medicament.
  • the present invention relates to a multispecific polypeptide construct comprising the antibody or functional fragment thereof of the present invention for use in the treatment of a disease, particularly a human disease, wherein said multispecific polypeptide construct comprises a second bioactive domain, which is able to specifically interact with a target of therapeutic relevance in the corresponding disease.
  • treatment refers to obtaining a desired pharmacologic and/or physiologic effect.
  • the effect may be therapeutic in terms of a partial or complete cure for a disease and/or adverse effect attributable to the disease or delaying the disease progression.
  • Treatment covers any treatment of a disease in a mammal, e.g., in a human, and includes: (a) inhibiting the disease, e.g., arresting its development; and (c) relieving the disease, e.g., causing regression of the disease.
  • present invention relates to the use of the antibody or functional fragment thereof of the present invention, or a multispecific polypeptide construct comprising the antibody or functional fragment thereof of the present invention in the manufacture of a medicament.
  • the present invention relates to a method of treating a subject suffering from a disease, particularly a human disease, comprising administering to said subject an effective amount of the antibody or functional fragment thereof of the present invention or a multispecific polypeptide construct comprising the antibody or functional fragment thereof of the present invention.
  • the present invention relates to a method of treating a subject suffering from a disease, particularly a human disease, comprising administering to said subject an effective amount of a multispecific polypeptide construct comprising the antibody or functional fragment thereof of the present invention, wherein said multispecific polypeptide construct comprises a second bioactive domain, which is able to specifically interact with a target of therapeutic relevance in the corresponding disease.
  • subject includes human and non-human animals.
  • Non-human animals include all vertebrates, e.g., mammals and non-mammals, such as non- human primates, sheep, dog, cow, chickens, amphibians, and reptiles.
  • said subject is human.
  • patient or subject are used herein interchangeably.
  • the term "effective amount” or “therapeutically effective amount” or “efficacious amount” refers to the amount of an agent that, when administered to a mammal or other subject for treating a disease, is sufficient to effect such treatment for the disease.
  • the “therapeutically effective amount” will vary depending on the agent, the disease and its severity and the age, weight, etc., of the subject to be treated.
  • the present invention relates to use of the antibody or functional fragment thereof of the present invention, or to a multispecific polypeptide construct comprising the antibody or functional fragment thereof of the present invention in the treatment of a disease, particularly a human disease, particularly wherein said multispecific polypeptide construct comprises a second bioactive domain, which is able to specifically interact with a target of therapeutic relevance in the corresponding disease.
  • Example 1 Selection and Humanization
  • the humanization of the selected clone comprised the transfer of the rabbit CDRs onto a scFv acceptor framework of the VK1 /VH3 type comprising a ⁇ framework IV sequence as described in WO 2014/206561 .
  • the amino acid sequence of the six CDR regions was identified on the donor sequence (rabbit mAb) and grafted into the acceptor scaffold sequence.
  • Additional amino acids from the rabbit donor in certain framework positions, which have been described to potentially influence CDR positioning and thus antigen binding were included in the final constructs (see Table 1 ).
  • the comparison of the characterization data for these constructs revealed a significant advantage over the CDR grafting alone.
  • the sequences of the resulting variable domains are shown in Table 2.
  • the heterologous expression of the proteins was performed in E.coli as insoluble inclusion bodies.
  • the expression culture was inoculated with an exponentially growing starting culture. The cultivation was performed in shake flasks in an orbital shaker using commercially available rich media. The cells were grown to a defined OD600 of 2 and induced by overnight expression with 1 mM Isopropyl ⁇ -D- 1 -thiogalactopyranoside (IPTG). At the end of fermentation the cells were harvested by centrifugation and homogenized by sonication. At this point the expression level of the different constructs was determined by SDS-PAGE analysis of the cell lysate.
  • the inclusion bodies were isolated from the homogenized cell pellet by a centrifugation protocol that included several washing steps to remove cell debris and other host cell impurities.
  • the purified inclusion bodies were solubilized in a denaturing buffer (100 mM Tris/HCI pH 8.0, 6 M Gdn-HCI, 2 mM EDTA) and the scFvs were refolded by a scalable refolding protocol that generated milligram amounts of natively folded, monomeric scFv.
  • a standardized protocol was employed to purify the scFvs, which included the following steps.
  • the product after refolding was captured by an affinity chromatography employing Capto L agarose (GE Healthcare) to yield the purified scFvs.
  • Affinity of the humanized scFvs to serum albumin (SA) of the different species was determined by SPR measurements using a MASS-1 device (Sierra Sensors). SA was directly coupled to a high capacity amine sensor chip (Sierra Sensors) using amine coupling chemistry. After performing a regeneration scouting and surface performance test to find best assay conditions, a scFv dose response was measured and obtained binding curves were double-referenced (empty reference channel and zero analyte injection) and fitted using the 1 :1 Langmuir model to retrieve kinetic parameters. The assay was run twice at different pH values: once in a 1 X PBS- Tween buffer at pH 5.5 and another time in a 1 X PBS-Tween buffer at pH 7.4.
  • An assay was set up at pH 5.5 to confirm that scFv-bound HSA is still capable of binding FcRn. This is necessary to allow the anti-HSA scFv or derivative thereof to be recycled with HSA through the interaction between HSA and FcRn.
  • An assay was developed using an HSA-immobilized chip: 1 . 90nM scFv was injected and the interaction was measured at low pH; 2. 90nM FcRn was injected and the interaction was measured at low pH 3. A 1 :1 mixture of scFv and FcRn (90nM each) was injected to see whether the sum of the binding levels of the individual injections approximates the binding level when the mixture is injected. If the scFv-bound HSA can no longer bind FcRn the binding level of the mixture would be the same as the binding level of the scFv alone.
  • variable domains as listed in Table 1 were arranged in an VLA-S1 -VHB-L1 -VLB-S2- VHA fashion, where S1 and S2 are short G 4 S linkers and L1 is a long (G 4 S) 4 linker.
  • PRO462 The resulting constructs with the aHSA domains and a second specificity for a second antigen were termed PRO462, in case of the domains 19-01 -H04-sc02, and PRO480, in case of the domains 23-13-A01 -sc02.
  • the nucleotide sequences were de novo synthesized and cloned into an adapted vector for E.coli expression that is based on a pET26b(+) backbone (Novagen).
  • the expression construct was transformed into the E.coli strain BL12 (DE3) (Novagen) and the cells were cultivated in 2YT medium (Sambrook, J., et al., Molecular Cloning: A Laboratory Manual) as a starting culture. Expression cultures were inoculated and incubated in shake flasks at 37°C and 200 rpm. Once an OD600 nm of 1 is reached protein expression was induced by the addition of IPTG at a final concentration of 0.5 mM.
  • the cells were harvested by centrifugation at 4000 g.
  • IB Resuspension Buffer 50 mM Tris-HCI pH 7.5, 100 mM NaCI, 5 mM EDTA, 0.5% Triton X-100.
  • the cell slurry was supplemented with 1 mM DTT, 0.1 mg/mL Lysozyme, 10 mM Leupeptin, 100 ⁇ PMSF and 1 ⁇ Pepstatin.
  • Cells were lysed by 3 cycles of ultrasonic homogenization while being cooled on ice. Subsequently 0.01 mg/mL DNAse was added and the homogenate was incubated at room temperature for 20 min.
  • the inclusion bodies were sedimented by centrifugation at 15000 g and 4°C.
  • the IBs were resuspended in IB Resuspension Buffer and homogenized by sonication before another centrifugation.
  • IB Wash Buffer 50 mM Tris-HCI pH 7.5, 100 mM NaCI, 5 mM EDTA
  • the isolated IBs were resuspended in Solubilization Buffer (100 mM Tris/HCI pH 8.0, 6 M Gdn-HCI, 2 mM EDTA) in a ratio of 5 mL per g of wet IBs.
  • Solubilization Buffer 100 mM Tris/HCI pH 8.0, 6 M Gdn-HCI, 2 mM EDTA
  • the solubilization was incubated for 30 min at room temperature until DTT was added at a final concentration of 20 mM and the incubation was continued for another 30 min. After the solubilization was completed the solution was cleared by 10 min centrifugation at 21500 g and 4°C.
  • the refolding was performed by rapid dilution at a final protein concentration of 0.3 g/L of the solubilized protein in Refolding Buffer (typically: 100 mM Tris-HCI pH 8.0, 5.0 M Urea, 5 mM Cysteine ⁇ mM Cystine).
  • Refolding Buffer typically: 100 mM Tris-HCI pH 8.0, 5.0 M Urea, 5 mM Cysteine ⁇ mM Cystine.
  • the refolding reaction was routinely incubated for a minimum of 14 h.
  • the resulting protein solution was cleared by 10 min centrifugation at 8500 g and 4°C.
  • the refolded protein was purified by affinity chromatography on Capto L resin (GE Healthcare).
  • the isolated monomer fraction was analyzed by size-exclusion HPLC, SDS-PAGE for purity and UV/Vis spectroscopy for protein content.
  • Buffer was exchange into Native buffer (50 mM Citrate-Phosphat
  • the midpoint of transition for the thermal unfolding of the tested constructs was determined by Differential Scanning Fluorimetry (DSF), essentially as described by Niesen (Niesen et al., Nat Protoc. 2 (2007) 2212-21 ).
  • the DSF assay is performed in a qPCR machine (e.g. MX3005p, Agilent Technologies).
  • the samples are diluted in buffer (citrate-phosphate pH 6.4, 0.25 M NaCI) containing a final concentration of 5x SYPRO orange in a total volume of 25 ⁇ _. Samples are measured in triplicates and a temperature ramp from 25-96°C programmed.
  • the fluorescence signal is acquired and the raw data is analyzed with the GraphPad Prism (GraphPad Software Inc.).
  • the protein degradation is assessed by SDS-PAGE analysis with Any kD Mini-Protean TGX gels (Bio-Rad Laboratories) and stained with Coomassie brilliant blue.
  • the protein concentration is monitored at the different time points by UV-Vis spectroscopy with an Infinity reader M200 Pro equipped with a Nanoquant plate (Tecan Group Ltd.).
  • the Fab-(scFv) 2 format is a multifunctional recombinant antibody derivative that employs a heterodimeric assembly of Fab fragments consisting of VL- CL and VH-CH1 with either constant domain forming a scaffold, upon which via flexible linkers additional binding domains, such as scFvs, can be incorporated (Schoonjans, Willems et al. 2001 ) (Schoonjans, Willems et al. 2000).
  • the molecules can be co-expressed in mammalian host cells such as CHO-S where the binding immunoglobulin chaperon drives heterodimerization of VL-CL and VH-CH1 domains even in presence of chain extensions. These heterodimers are stable, with each of the binders retaining their specific affinities. ScFv fusions at positions CL and CH1 of the Fab-(scFv) 2 molecule are considered as equivalent.
  • the only non-natural sequence fragments in the molecule are peptide linkers connecting variable domains within scFv domains and scFv domains with Fab constant domains are composed of glycin-serine-polymers which are considered to be neither antigenic nor immunogenic.
  • PR0497 is a Fab-(scFv) 2 molecule comprising an anti-CD3 specific (09-24-H09-sc04) Fab portion with an anti-HSA specific scFv domain (23-13-A01 - sc02) fused to the CL domain and an anti-IL23R specific scFv domain (14-1 1 -D07- sc04) fused to the CH1 domain. Domains within scFv domains are connected via 20 amino acid (G 4 S) 4 linkers while individual scFv domains are fused via 15 amino acid (G 4 S) 3 peptide linkers to the Fab fragment.
  • Pre-dose 10 and 30 min and 1 , 2, 4, 6, 8, 12, 24, 36, 48, 72, 96, 144, 192, 240, 288, 336, 384, 432 and 504 h post-dose.
  • VL (12V, Q3V, K50Q, A51P)
  • VH (155V, V103T, Y105F)
  • Table 3 Affinity measurement of humanized scFv constructs derived from clone 19-01-H04 and 23-13- A01. The binding kinetics for human and cynomolgus serum albumin were determined at pH 5.5 and pH 7.4.
  • Table 4 Affinity measurement of humanized scFv constructs derived from clone 19-01-H04 and 23-13- A01. The binding kinetics for mouse and rat serum albumin were determined at pH 5.5 and pH 7.4. Measurements of marmoset serum album were made at pH 5.5. 5.5 5.5

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Abstract

La présente invention concerne de nouveaux anticorps qui sont spécifiques du sérum humain.
PCT/EP2018/064622 2017-06-05 2018-06-04 Nouveaux anticorps anti-hsa WO2018224439A1 (fr)

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KR1020197035189A KR20200015505A (ko) 2017-06-05 2018-06-04 신규 항 hsa 항체
CA3064160A CA3064160A1 (fr) 2017-06-05 2018-06-04 Nouveaux anticorps anti-hsa
JP2019566084A JP7130678B2 (ja) 2017-06-05 2018-06-04 新規抗ｈｓａ抗体
CN201880036722.9A CN110709418B (zh) 2017-06-05 2018-06-04 新型抗hsa抗体
AU2018280679A AU2018280679A1 (en) 2017-06-05 2018-06-04 Novel anti-HSA antibodies
IL271127A IL271127B2 (en) 2017-06-05 2018-06-04 New anti-HSA antibodies
US16/618,864 US11365240B2 (en) 2017-06-05 2018-06-04 Anti-HSA antibodies
EP18729642.1A EP3634997A1 (fr) 2017-06-05 2018-06-04 Nouveaux anticorps anti-hsa

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WO2020099871A1 (fr) * 2018-11-13 2020-05-22 Crescendo Biologics Limited Anticorps à domaine unique se liant à l'albumine sérique humaine
WO2020157305A1 (fr) * 2019-01-31 2020-08-06 Numab Therapeutics AG Anticorps multispécifiques ayant une spécificité pour tnfa et il-17a, anticorps ciblant il-17a, et leurs procédés d'utilisation
US11591398B2 (en) 2017-01-06 2023-02-28 Crescendo Biologics Limited Single domain antibodies to programmed cell death protein 1 (PD-1)
WO2023242371A1 (fr) * 2022-06-15 2023-12-21 argenx BV Molécules de liaison hsa dépendantes du ph et procédés d'utilisation
US11951172B2 (en) 2018-02-16 2024-04-09 Crescendo Biologics Limited Therapeutic molecules that bind to LAG3 and PD1
US12077595B2 (en) 2017-11-13 2024-09-03 Crescendo Biologics Limited Single domain antibodies that bind to CD137

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US11591398B2 (en) 2017-01-06 2023-02-28 Crescendo Biologics Limited Single domain antibodies to programmed cell death protein 1 (PD-1)
US11814429B2 (en) 2017-01-06 2023-11-14 Crescendo Biologics Limited Single domain antibodies to programmed cell death (PD-1)
US12077595B2 (en) 2017-11-13 2024-09-03 Crescendo Biologics Limited Single domain antibodies that bind to CD137
US11951172B2 (en) 2018-02-16 2024-04-09 Crescendo Biologics Limited Therapeutic molecules that bind to LAG3 and PD1
WO2020099871A1 (fr) * 2018-11-13 2020-05-22 Crescendo Biologics Limited Anticorps à domaine unique se liant à l'albumine sérique humaine
CN113412278A (zh) * 2018-11-13 2021-09-17 克雷森多生物制剂有限公司 结合人血清白蛋白的单结构域抗体
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CN113631574A (zh) * 2019-01-31 2021-11-09 努玛治疗有限公司 对TNFα和IL-17A具有特异性的多特异性抗体、靶向IL-17A的抗体及其使用方法
JP2022523908A (ja) * 2019-01-31 2022-04-27 ヌマブ セラピューティクス アクチェンゲゼルシャフト ＴＮＦα及びＩＬ－１７Ａに対する特異性を有する多重特異性抗体、ＩＬ－１７Ａを標的とする抗体、及びそれらの使用方法
JP7525499B2 (ja) 2019-01-31 2024-07-30 ヌマブ セラピューティクス アクチェンゲゼルシャフト ＴＮＦα及びＩＬ－１７Ａに対する特異性を有する多重特異性抗体、ＩＬ－１７Ａを標的とする抗体、及びそれらの使用方法
WO2023242371A1 (fr) * 2022-06-15 2023-12-21 argenx BV Molécules de liaison hsa dépendantes du ph et procédés d'utilisation

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