US20240043521A1 - Anti-S100A4 Humanized Antibodies, Uses and Methods - Google Patents

Anti-S100A4 Humanized Antibodies, Uses and Methods Download PDF

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US20240043521A1
US20240043521A1 US18/264,483 US202218264483A US2024043521A1 US 20240043521 A1 US20240043521 A1 US 20240043521A1 US 202218264483 A US202218264483 A US 202218264483A US 2024043521 A1 US2024043521 A1 US 2024043521A1
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antibody
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Jonas Hallén
Rizwan Iqbal Hussain
Jörg Klingelhöfer
Tim Buss
Darragh MacCann
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Calluna Pharma Inc
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Arxx Therapeutics AS
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/24—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/10—Immunoglobulins specific features characterized by their source of isolation or production
    • C07K2317/14—Specific host cells or culture conditions, e.g. components, pH or temperature
    • 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
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/52—Constant or Fc region; Isotype
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C07K2317/565—Complementarity determining region [CDR]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C07K2317/567—Framework region [FR]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/71—Decreased effector function due to an Fc-modification
    • 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

Definitions

  • the present invention relates to isolated anti-S100A4 humanized antibody molecules and their medical uses, and more particularly to isolated anti-S100A4 humanized antibody molecules that are capable of inhibiting the biological activity of S100A4, for example in promoting chronic inflammation, fibrosis, tumour progression and/or in inducing tumour metastasis, and their uses in the treatment of fibrotic disease, inflammatory conditions, and cancer, in particular metastatic cancer.
  • Fibrosis is defined as an excessive deposition of extracellular matrix proteins.
  • the early stages of fibrotic disease are almost always characterised by an inflammatory response that functions to attract, differentiate and activate fibroblasts which in turn produce collagen and other extracellular matrix proteins. If these processes become chronic, the inflammatory and/or fibrotic responses gradually undermine physiological tissue function and may lead to organ compromise or failure.
  • the mechanisms involved in chronic inflammation and fibrosis are underlying drivers of a wide range of diseases with different clinical manifestations, which include, in addition to pure fibrotic and inflammatory conditions, atherosclerosis, cancer and neurodegenerative disease.
  • a diseased tissue microenvironment provides an essential support mechanism for malignant cells to proliferate and spread.
  • the activation of inflammatory and fibrotic pathways play an important role in the development of pre-metastatic niches that provide the necessary conditions for primary tumour cells to spread to distant organs.
  • S100A4 has been identified as a key protein involved in the processes that amplify and sustain inappropriate activation of inflammatory and fibrotic pathways.
  • S100A4 belongs to the S100 family of small Ca-binding proteins with diverse extra- and intra-cellular function (Donato, 2003). Under physiological conditions, S100A4 is predominantly located intracellularly, but is released to the extracellular environment upon cell stress or injury (Fei et al., 2017). Extracellular S100A4 forms higher order oligomers that engage Pattern Recognition Receptors (PRRs) which in turn activate multiple inflammatory and fibrotic responses (Ambartsumian et al., 2019; Fei et al., 2017).
  • PRRs Pattern Recognition Receptors
  • S100A4 Through interaction with PRRs, S100A4 triggers release of inflammatory mediators from immune cells, stimulates the release of extracellular matrix proteins from fibroblasts, and is involved in epithelial-to-mesenchymal transition (Kalluri & Zeisberg, 2006; Tomcik et al., 2015; Neidhart et al., 2019). Overexpression of S100A4 is a hallmark of chronic inflammation and fibrosis.
  • S100A4 is causally involved in the pathogenesis of inflammation and fibrosis (Ambartsumian et al., 2019). Knockdown of S100A4 in fibroblasts prevents the TGF ⁇ induced activation of fibroblasts (Tomcik et al., 2015). Knockout of S100A4 inhibits fibrosis, inflammation and cancer spread in several animal models including bleomycin-induced skin or pulmonary fibrosis, tight-skin 1 skin fibrosis and several cancer models (Ambartsumian et al., 2019; Tomcik et al., 2015).
  • S100A4 activity is associated with stimulation of cancer cell motility and invasion, normal and aberrant proliferation, apoptosis and differentiation. It is involved in signalling pathways leading to the remodelling of the cell membrane and the extracellular matrix; modulation of cytoskeletal dynamics, acquisition of invasiveness and induction of angiogenesis (Sherbet, 2009).
  • S100A4 is expressed in certain tumour cells, but more generally it is activated and secreted from certain cancer-associated stroma cells which lead to its accumulation in the tumour microenvironment. Moreover, it has been shown that the metastatic microenvironment contains greater numbers of S100A4-positive stromal cells than the primary tumour microenvironment (Cabezon et al., 2007; Grum-Schwensen et al., 2005; 2010; Maelandsmo et al., 2009; Schmidt-Hansen, et al., 2004a).
  • S100A4 has been shown to maintain the stemness properties and tumorigenicity of cancer-initiating cells in head and neck cancers and glioblastoma (Lo et al., 2011; Chow et al., 2017). Development of drugs capable of inhibiting the bioactivity of S100A4 may therefore represent a promising therapeutic option to modulate multiple inflammatory and fibrotic pathways that are activated in a range of human diseases. There is thus an unmet need for therapeutic anti-S100A4 antibodies, particularly humanized anti-S100A4 antibodies, as they would specifically target the extracellular, disease-causing fraction of S100A4.
  • Humanized antibodies are antibodies from non-human species whose protein sequences have been modified to increase their similarity to antibody variants produced naturally in humans.
  • the process of “humanization” is usually applied to monoclonal antibodies developed for administration to humans (for example, antibodies developed as anti-cancer drugs). Humanization can be necessary when the process of developing a specific antibody involves generation in a non-human immune system (such as that in mice).
  • the protein sequences of antibodies produced in non-human immune systems are partially distinct from homologous antibodies occurring naturally in humans, and are therefore potentially immunogenic when administered to human patients, which can remove any therapeutic benefit and potentially cause adverse effects in the patient.
  • the present invention provides a humanized anti-s100A4 antibody with an improved safety profile.
  • the inventors have found that murine IgG1 and humanized IgG1 anti-S100A4 antibodies elicit a counterintuitive increase in the pro-inflammatory cytokine TNF ⁇ , while at the same time blocking the S100A4 stimulated increase of IL-6 and IL-10.
  • the increase in TNF ⁇ is elicited through Fc ⁇ RIIA receptor clustering and activation.
  • This effect is surprisingly dependent on both the anti-S100A4 antibody and the S100A4 protein, as neither anti-S100A4 antibody in the absence of S100A4, nor S100A4 in combination with an isotype control antibody (either human IgG1 or human IgG4) resulted in Fc ⁇ RIIA receptor clustering.
  • the inventors have found that a subclass switch of the humanized anti-S100A4 antibody from an IgG1 scaffold to an IgG4 scaffold attenuates this previously unreported S100A4-dependent Fc ⁇ RIIA receptor clustering and activation, thus preventing unwanted pro-inflammatory cytokine release and improving the safety profile of the antibody.
  • the Fc ⁇ RIIA receptor clustering and activation by the humanized IgG4 antibody is also significantly decreased compared to that elicited by murine IgG1 anti-S100A4 antibodies.
  • an isolated antibody comprising:
  • an isolated antibody comprising:
  • an isolated nucleic acid molecule encoding the antibody as described herein above in the section ‘Isolated anti-S100A4 antibody molecule’.
  • an expression vector comprising the nucleic acid molecule as described herein encoding an anti-S100A4 antibody molecule.
  • an isolated host cell comprising the isolated nucleic acid molecule or the expression vector as described herein.
  • a method of producing an anti-S100A4 antibody molecule comprising culturing the host cell as described herein under conditions wherein the antibody is expressed.
  • a pharmaceutical composition comprising the antibody, the nucleic acid molecule, the expression vector and/or the host cell as described herein, and a pharmaceutically acceptable diluent, carrier and/or excipient.
  • a method of treatment of an individual with an S100A4-mediated condition comprising administering the antibody or the host cell as described herein to an individual in need thereof.
  • a method for diagnosis or prognosis of an S100A4-related condition in an individual comprising
  • FIG. 1 shows the effects of monoclonal humanized anti-S100A4 antibodies on fibrotic readouts in bleomycin-challenged mice. Effects of anti-S100A4 antibodies on dermal thickness (A), myofibroblast counts (B) and hydroxyproline content (C). Representative images of HE stained skin sections are shown in D-E. P-values are expressed as follows: 0.05>p>0.01 as *; 0.01>p>0.001 as ** as compared to NaCl; 0.05>p>0.01 as #; 0.01>p>0.001 as ## as compared to mice injected with bleomycin for three weeks followed by injections of NaCl for another 3 weeks. The results are further described in Example 3.
  • FIG. 2 shows IL-6 secretion by monocytes analysed by Luminex analysis. Data shown is the average of 5 donors. Monocytes purified from PBMC were cultured with media, vehicle, LPS, S100A4 in the absence or presence of mouse IgG1 (A), human IgG4 (B), AX-202 (C) or 6B12 (D) for 6 hours. Data shows levels of IL-6 in the supernatant quantified by Luminex assay. Data presented as mean+SEM arising from five independent donors. “+” indicates at least one donor above the limit of detection for IL-6 (19,200 pg/mL). “ ⁇ ” indicates at least one donor below the limit of detection for IL-6 (8.8 pg/mL). The results are further described in Example 4.
  • FIG. 3 shows IL-10 secretion by monocytes analysed by Luminex analysis. Data shown is the average of 5 donors. Monocytes purified from PBMC were cultured with media, vehicle, LPS, S100A4 in the absence or presence of mouse IgG1 (A), human IgG4 (B), AX-202 (C) or 6B12 (D) for 6 hours. Data shows IL-10 of cytokine in the supernatant quantified by Luminex assay. Data presented as mean+SEM arising from five independent donors. “ ⁇ ” indicates at least one donor below the limit of detection for IL-10 (8.6 pg/mL). The results are further described in Example 4.
  • FIG. 4 shows TNF- ⁇ secretion by monocytes analysed by Luminex analysis. Data shown is the average of 5 donors. Monocytes purified from PBMC were cultured with media, vehicle, LPS, S100A4 in the absence or presence of mouse IgG1 (A), human IgG4 (B), AX-202 (C) or 6B12 (D) for 6 hours. Data shows levels of TNF- ⁇ in the supernatant quantified by Luminex assay. Data presented as mean+SEM arising from five independent donors. “ ⁇ ” indicates at least one donor below the limit of detection for TNF- ⁇ (15.20 pg/ml). The results are further described in Example 4.
  • FIG. 5 shows the specificity of three humanized variants of 6B12 mAb to different other S100 family members as measured by Western blotting. The results are further described in Example 5.
  • FIG. 7 shows that AX-202 inhibits S100A4-induced TLR4 activation in a concentration-dependent manner.
  • S100A4 activates NF-k6 reporter gene in HEKBlue hTLR4 cells in a concentration-dependent manner.
  • B S100A4 activation of the NF-k6 reporter gene is dependent on TLR4.
  • C AX-202 inhibits S100A4-induced TLR4 activation in a concentration-dependent manner. The results are further described in Example 6.
  • FIG. 8 shows a comparison of the Fc ⁇ IIaR binding activity for 2 ⁇ g/ml 6B12 mIgG1, AX-202 hIgG1 and AX-202 hIgG4 when combined with either 2.5 ⁇ g/ml recombinant human S100A4 dimer (A) or multimer (B).
  • the control IgG1 or IgG4 antibodies did not mediate receptor clustering and activation.
  • the protein S100A4 is also known as 18A2, 42A, CAPL, FSP1, MTS1, P9KA, PEL98 and S100 calcium binding protein A4.
  • isolated refers to a compound which can be e.g. an antibody or an antigen binding moiety that is substantially free of other antibodies or antigen binding moieties having different antigenic specificities. Moreover, an isolated antibody antigen binding moiety may be substantially free of other cellular material and/or chemicals.
  • Operably linked as defined herein refers to the mentioned elements being joined as part of the same nucleic acid molecule, suitably positioned and oriented for transcription to be initiated from the promoter.
  • DNA operably linked to a promoter is under transcriptional initiation regulation of the promoter or in functional combination therewith.
  • variant defines either a naturally occurring genetic mutant of a DNA sequence or its encoded RNA or protein product, or a recombinantly prepared variation of a DNA sequence or its encoded RNA or protein product.
  • variant may also refer to either a naturally occurring variation of a given peptide or a recombinantly prepared variation of a given peptide or protein in which one or more amino acid residues have been modified by amino acid substitution, addition, or deletion.
  • “Inhibition” as used herein means that the presence of the antibody of the invention inhibits, in whole or in part, the binding of ligands to their receptor and/or the disablement of a signal the receptor would elicit upon ligand binding. This includes for example down-stream signalling having effect on cellular behaviour and processes. Also included are other mechanisms of inhibiting the downstream effects of the targeted molecule, such as by blocking dimerization, oligomerization and/or multimerization of the target molecule. “Inhibition”, “blocking” and “neutralizing” are used herein as equivalent terms.
  • an isolated antibody comprising:
  • the heavy chain variable (VH) region of the isolated antibody comprises:
  • the heavy chain variable (VH) region of the isolated antibody comprises:
  • an isolated antibody comprising:
  • the heavy chain variable (VH) region of the antibody comprises or consists of an amino acid sequence as defined by SEQ ID NO: 13. In some embodiments, the heavy chain variable (VH) region of the antibody comprises or consists of an amino acid sequence as defined by SEQ ID NO: 14. In some embodiments, the heavy chain variable (VH) region of the antibody comprises or consists of an amino acid sequence as defined by SEQ ID NO: 15. In some embodiments, the heavy chain variable (VH) region of the antibody comprises or consists of an amino acid sequence as defined by SEQ ID NO: 16. In some embodiments, the heavy chain variable (VH) region of the antibody comprises or consists of an amino acid sequence as defined by SEQ ID NO: 17.
  • the heavy chain variable (VH) region of the antibody comprises or consists of a variant of any one of the amino acid sequences as defined by SEQ ID NO:s 13 to 17, wherein any one amino acid has been altered for another amino acid, with the proviso that no more than 5 amino acids have been so altered, for example wherein 5, 4, 3, 2, or 1 amino acid has been so altered in each amino acid sequence.
  • the light chain variable (VL) region of the antibody comprises or consists of an amino acid sequence as defined by SEQ ID NO: 18. In some embodiments, the light chain variable (VL) region of the antibody comprises or consists of an amino acid sequence as defined by SEQ ID NO: 19. In some embodiments, the light chain variable (VL) region of the antibody comprises or consists of an amino acid sequence as defined by SEQ ID NO: 20. In some embodiments, the light chain variable (VL) region of the antibody comprises or consists of an amino acid sequence as defined by SEQ ID NO: 21. In some embodiments, the light chain variable (VL) region of the antibody comprises or consists of an amino acid sequence as defined by SEQ ID NO: 22.
  • the light chain variable (VL) region of the antibody comprises or consists of a variant of any one of the amino acid sequences as defined by SEQ ID NO:s 18 to 22, wherein any one amino acid has been altered for another amino acid, with the proviso that no more than 5 amino acids have been so altered, for example wherein 5, 4, 3, 2, or 1 amino acid has been so altered in each amino acid sequence.
  • the antibody is a bispecific antibody.
  • the antibody is a full-length antibody. In some embodiments, the antibody is a Fab fragment. In some embodiments, the antibody is a F(ab′) fragment. In some embodiments, the antibody is a F(ab′) 2 fragment. In some embodiments, the antibody is a scFv. In some embodiments, the antibody is a diabody. In some embodiments, the antibody is a triabody.
  • the antibody is a human IgG1 immunoglobulin subclass antibody. In some embodiments, the antibody is a human IgG2 immunoglobulin subclass antibody. In some embodiments, the antibody is a human IgG3 immunoglobulin subclass antibody.
  • the inventors have found that, compared to vehicle controls, S100A4-induced TNF ⁇ levels were not increased by mouse IgG1 or human IgG4 isotype controls, however 6B12 (mouse IgG1 anti-S100A4 antibody) significantly increased S100A4-induced TNF ⁇ levels, and this increase was absent in a humanized IgG4 anti-S100A4 antibody (for further details see Examples 4 and 7).
  • 6B12 mouse IgG1 anti-S100A4 antibody
  • 6B12 mouse IgG1 anti-S100A4 antibody
  • the human IgG4 subclass may in particular be useful when reduced effector or cross-linking functions of the antibody are desired.
  • the antibody is therefore a human IgG4 subclass antibody.
  • the antibody is a human IgG4 subclass antibody with the HC sequence of SEQ ID NO: 58 and a LC sequence of SEQ ID NO: 59.
  • the antibody comprises a human heavy chain constant (CH) region comprising or consisting of the sequence as set forth in SEQ ID NO: 56.
  • the antibody comprises a CH region comprising or consisting of a variant of SEQ ID NO: 56, said variant having at least 80%, such as at least 81%, such as at least 82%, such as at least 83%, such as at least 84%, such as at least 85%, such as at least 86%, such as at least 87%, such as at least 88%, such as at least 89%, such as at least 90%, such as at least 91%, such as at least 92%, such as at least 93%, such as at least 94%, such as at least 95%, such as at least 96%, such as at least 97%, such as at least 98%, such as at least 99% sequence identity thereto.
  • CH human heavy chain constant
  • the antibody comprises a human light chain constant (CL) region comprising or consisting of the sequence as set forth in SEQ ID NO: 57.
  • the antibody comprises a CL region comprising or consisting of a variant of SEQ ID NO: 57, said variant having at least 80%, such as at least 81%, such as at least 82%, such as at least 83%, such as at least 84%, such as at least 85%, such as at least 86%, such as at least 87%, such as at least 88%, such as at least 89%, such as at least 90%, such as at least 91%, such as at least 92%, such as at least 93%, such as at least 94%, such as at least 95%, such as at least 96%, such as at least 97%, such as at least 98%, such as at least 99% sequence identity thereto.
  • the antibody comprises an Fc domain with a mutated human IgG constant region. In some embodiments, the antibody comprises a mutant human IgG4 heavy chain constant region. In some embodiments, said mutant human IgG4 heavy chain constant region comprises an S228P substitution, numbering according to EU numbering. Said S228P substitution may prevent in vivo and in vitro IgG4 Fab-arm exchange, which can result in functionally monovalent, bispecific antibodies (bsAbs) with unknown specificity and therefore, potentially, reduced therapeutic effect. In some embodiments, the terminal lysine of the human IgG4 heavy chain constant region has been removed.
  • the first humanized antibody was made in 1986 by Greg Winter's lab in Cambridge, UK. This antibody suffered a moderate loss of affinity but the strategy of CDR grafting murine CDR's onto human framework was considered a success.
  • the next antibody to be humanized was the therapeutic antibody Campath-1 which suffered marked reduction in affinity and it was here that framework amino acids important for CDR stability and VH/VL interface stability first started to be explored.
  • framework amino acids play a key role in presenting the CDR's in a way favorable to their antigen binding, however no automatic or routine method of identifying and deciding which residues to back-mutate for successful increase of antigen affinity exist. It is important to consider which positions are important for stability of the VL/VH interface and the frequency of each amino acid at the given position in similar antibody frameworks. Framework back mutations may thus be useful for improving the affinity or stability of the humanized antibody to its target.
  • the antibody comprises an amino acid substitution of the amino acid at position 40 of the VH region of any one of SEQ ID NO:s 13 to 17 to phenylalanine. In some embodiments, the antibody comprises an amino acid substitution of the amino acid at position 43 of the VH region of any one of SEQ ID NO:s 13 to 17 to serine. In some embodiments, the antibody comprises an amino acid substitution of the amino acid at position 44 of the VH region of any one of SEQ ID NO:s 13 to 17 to lysine.
  • the antibody comprises an amino acid substitution of the amino acid at position 42 of the VL region of any one of SEQ ID NO:s 18 to 22 to glycine. In some embodiments, the antibody comprises an amino acid substitution of the amino acid at position 43 of the VL region of any one of SEQ ID NO:s 18 to 22 to threonine. In some embodiments, the antibody comprises an amino acid substitution of the amino acid at position 44 of the VL region of any one of SEQ ID NO:s 18 to 22 to leucine.
  • the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 24. In some embodiments, the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 25. In some embodiments, the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 26. In some embodiments, the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 27. In some embodiments, the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 28. In some embodiments, the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 29.
  • the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 30. In some embodiments, the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 31. In some embodiments, the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 32. In some embodiments, the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 33. In some embodiments, the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 34. In some embodiments, the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 35.
  • the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 36. In some embodiments, the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 37. In some embodiments, the VH region of the antibody comprises or consists of a VH region as defined in SEQ ID NO: 38.
  • the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 39. In some embodiments, the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 40. In some embodiments, the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 41. In some embodiments, the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 42. In some embodiments, the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 43. In some embodiments, the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 44.
  • the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 45. In some embodiments, the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 46. In some embodiments, the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 47. In some embodiments, the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 48. In some embodiments, the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 49. In some embodiments, the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 50.
  • the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 51. In some embodiments, the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 52. In some embodiments, the VL region of the antibody comprises or consists of a VL region as defined by SEQ ID NO: 53.
  • the VH region of the antibody comprises or consists of SEQ ID NO: 24 (VH1_H40Phe) and the VL region of the antibody comprises or consists of SEQ ID NO: 47 (VL3_L44Leu).
  • the VH region of the antibody comprises or consists of SEQ ID NO: 24 (VH1_H40Phe) and the VL region of the antibody comprises or consists of SEQ ID NO: 20 (VL3).
  • the VH region of the antibody comprises or consists of SEQ ID NO: 26 (VH1_H44Lys) and the VL region of the antibody comprises or consists of SEQ ID NO: 20 (VL3).
  • the VH region of the antibody comprises or consists of SEQ ID NO: 13 (VH1) and the VL region of the antibody comprises or consists of SEQ ID NO: 47 (VL3_L44Leu). In some embodiments, the VH region of the antibody comprises or consists of SEQ ID NO: 13 (VH1) and the VL region of the antibody comprises or consists of SEQ ID NO: 20 (VL3).
  • the antibody is PEGylated.
  • the antibody according to the present invention is capable of binding to native conformation S100A4 protein. In some embodiments, the antibody is capable of binding to dimeric forms of S100A4 protein. In some embodiments, the antibody is capable of binding to oligomeric forms of S100A4 protein. In some embodiments, the antibody is capable of binding to multimeric forms of S100A4 protein.
  • the antibody is capable of binding to a polypeptide having at least 80% sequence identity to amino acids 1 to 101 as set out in SEQ ID NO: 23 (human S100A4). In some embodiments, the antibody is capable of binding to a polypeptide having at least 85% sequence identity to amino acids 1 to 101 as set out in SEQ ID NO: 23. In some embodiments, the antibody is capable of binding to a polypeptide having at least 90% sequence identity to amino acids 1 to 101 as set out in SEQ ID NO: 23. In some embodiments, the antibody is capable of binding to a polypeptide having at least 95% sequence identity to amino acids 1 to 101 as set out in SEQ ID NO: 23. In some embodiments, the antibody is capable of binding to human S100A4 polypeptide of SEQ ID NO: 23.
  • the antibody is capable of neutralizing a biological activity of S100A4.
  • the biological activity of S100A4 is in promoting tumor progression and/or in inducing tumor metastasis.
  • treatment with the anti-S100A4 antibody reduces fibrosis.
  • the antibody is capable of reducing S100A4-mediated fibrosis. Fibrosis may be assessed by measuring dermal thickness, dermal hydroxyproline content, dermal CD3 + cell count and/or dermal myofibroblast counts by methods known in the art.
  • treatment with the anti-S100A4 antibody reduces dermal thickness, dermal collagen or hydroxyproline content, dermal myoblast count and/or T-cell count.
  • the antibody is capable of inhibiting the biological activity of S100A4 in promoting tumor progression and/or in inducing tumor metastasis and/or in inflammation.
  • the antibody is capable of inhibiting T-cell recruitment mediated by S100A4. In some embodiments, the antibody is capable of inhibiting macrophage recruitment and/or infiltration mediated by S100A4.
  • the antibody is capable of inhibiting the biological activity of S100A4 protein in stimulating cell invasion.
  • the biological activity of S100A4 protein in stimulating cell invasion is determined in a 3D Matrigel matrix assay or a T cell invasion assay where S100A4 stimulates T cell infiltration into a fibroblasts monolayer.
  • the biological activity of S100A4 in inducing tumor metastasis is determined in an in vivo mouse xenograft model.
  • the antibody has low or no effector function. In some embodiments, the antibody induces low or no binding, cross-linking and/or activation of Fc receptor dependent effector functions of host cells.
  • an isolated nucleic acid molecule encoding the antibody as described herein above in the section ‘Isolated anti-S100A4 antibody molecule’.
  • the nucleic acid molecule is codon-optimized for the cell wherein it is expressed.
  • an expression vector comprising the nucleic acid molecule as described herein encoding an anti-S100A4 antibody molecule.
  • the nucleic acid molecule of said expression vector is operably linked to control sequences to direct its expression.
  • control sequences include regulatory elements that may control transcription of the sequence encoding the anti-S100A4 antibody molecule, e.g. promoters (such as those activated by transcription factors), enhancers or silencers.
  • translation of the mRNA encoding the encoding the anti-S100A4 antibody molecule may be controlled by a different control element, such as a riboswitch. Suitable control sequences and vectors are well known in the art.
  • Suitable techniques for producing and manipulating nucleic acids and expressing it in cells are well known in the art by the person of ordinary skill.
  • an isolated host cell comprising the isolated nucleic acid molecule or the expression vector as described herein above in the section ‘Nucleic acid and expression vector’.
  • the isolated host cell is a human cell. In some embodiments, the isolated host cell is Chinese hamster ovary (CHO) cell.
  • the current invention may also be used in connection with ex vivo gene therapy, wherein patient cells are transfected or transduced in vitro with an expression vector coding for an antibody as disclosed herein. After transfection, the cells are infused back into the patient to express and secrete the antibody.
  • Suitable donor cells for ex vivo gene therapy include T-cells.
  • a method of producing an anti-S100A4 antibody molecule comprising culturing the host cell as described herein above in the section ‘Host cells comprising the antibody’ under conditions wherein the antibody is expressed.
  • the method further comprises purifying the antibody and isolating the anti-S100A4 antibody thus produced.
  • a pharmaceutical composition comprising the antibody as described herein above in the section ‘Isolated anti-S100A4 antibody molecule’, the nucleic acid molecule and/or the expression vector as described herein above in the section ‘Nucleic acid and expression vector encoding the antibody’, and/or the host cell as described herein above in the section ‘Host cells comprising the antibody’, and a pharmaceutically acceptable diluent, carrier and/or excipient.
  • a method of treatment of an individual with an S100A4-mediated condition comprising administering the antibody as described herein above in the section ‘Isolated anti-S100A4 antibody molecule’, the nucleic acid molecule and/or the expression vector as described herein above in the section ‘Nucleic acid and expression vector encoding the antibody’, or the host cell as described herein above in the section ‘Host cells comprising the antibody’ to an individual in need thereof.
  • the S100A4-mediated condition is a fibrotic condition.
  • the fibrotic condition is systemic sclerosis. In some embodiments, the fibrotic condition is skin fibrosis. In some embodiments, the fibrotic condition is interstitial pulmonary fibrosis. In some embodiments, the fibrotic condition is liver fibrosis. In some embodiments, the fibrotic condition is kidney fibrosis.
  • the antibody is co-administered with another compound for treatment of systemic sclerosis.
  • the antibody is co-administered with an angiotensin-converting enzyme inhibitor.
  • the antibody is co-administered with an angiotensin receptor blocker.
  • the antibody is co-administered with an azathioprine.
  • the antibody is co-administered with a calcium channel blocker.
  • the antibody is co-administered with a cyclophosphamide.
  • the antibody is co-administered with a hydroxychloroquine. In some embodiments, the antibody is co-administered with a mycophenolate. In some embodiments, the antibody is co-administered with a methotrexate. In some embodiments, the antibody is co-administered with a glucocorticoid. In some embodiments, the antibody is co-administered with a phosphodiesterase-5 inhibitor. In some embodiments, the antibody is co-administered with an endothelin receptor antagonist. In some embodiments, the antibody is co-administered with an alpha blocker.
  • the antibody is co-administered with a prostanoid. In some embodiments, the antibody is co-administered with rituximab. In some embodiments, the antibody is co-administered with a tyrosine kinase inhibitor such as nintedanib. In some embodiments, the antibody is co-administered with tociluzimab.
  • the S100A4-mediated condition is an inflammatory condition.
  • the inflammatory condition is psoriasis.
  • the inflammatory condition rheumatoid arthritis.
  • the inflammatory condition is inflammatory myopathy.
  • the S100A4-mediated condition is cancer.
  • the cancer is metastatic cancer.
  • the cancer is gastric cancer. In some embodiments, the cancer is pancreatic cancer. In some embodiments, the cancer is colorectal cancer. In some embodiments, the cancer is thyroid cancer. In some embodiments, the cancer is breast cancer. In some embodiments, the cancer is squamous cell carcinoma. In some embodiments, the cancer is non-small cell lung cancer. In some embodiments, the cancer is prostate cancer. In some embodiments, the cancer is lung cancer. In some embodiments, the cancer is head and neck cancer. In some embodiments, the cancer is brain cancer (including glioblastoma multiforme). In some embodiments, the cancer is renal cell carcinoma (including clear cell renal carcinoma). In some embodiments, the cancer is melanoma.
  • the cancer is lymphoma. In some embodiments, the cancer is plasmocytoma. In some embodiments, the cancer is sarcoma. In some embodiments, the cancer is glioma. In some embodiments, the cancer is thymoma. In some embodiments, the cancer is leukemia. In some embodiments, the cancer is colon cancer. In some embodiments, the cancer is esophageal cancer. In some embodiments, the cancer is ovary cancer. In some embodiments, the cancer is cervical cancer. In some embodiments, the cancer is hepatoma.
  • the antibody, nucleic acid molecule, expression vector, and/or host cell is administered via parenteral administration.
  • the antibody, nucleic acid molecule, expression vector, and/or host cell is administered subcutaneously.
  • the antibody, nucleic acid molecule, expression vector, and/or host cell is administered intramuscularly.
  • the antibody, nucleic acid molecule, expression vector, and/or host cell is administered intravenously.
  • the antibody, nucleic acid molecule, expression vector, and/or host cell is administered once every week or less. In some embodiments, the antibody is administered weekly, with a weekly dosage of in the range of 15 mg to 1000 mg.
  • a method for diagnosis or prognosis of an S100A4-related condition in an individual comprising
  • the biological sample is blood. In some embodiments, the biological sample is plasma. In some embodiments, the biological sample is serum. In some embodiments, the biological sample is a tissue sample. In some embodiments, the biological sample is interstitial tissue fluids. In some embodiments, the biological sample is saliva. In some embodiments, the biological sample is cerebrospinal fluid. In some embodiments, the biological sample is synovia.
  • the closest human germline gene V-region to the VH region was identified as Homo sapiens IGHV4-34*09.
  • Databases of Human IgG sequences were searched for comparison to the murine VH domain using BLAST search algorithms, and candidate human variable domains selected from the top 200 BLAST results. These were reduced to four candidates for each based on a combination of framework homology, maintaining key framework residues and canonical loop structure.
  • the closest human germline IGHV4-34*09 was selected.
  • the closest human germline gene V-region to the VL region was identified as the Homo sapiens IGKV1-27.
  • Databases of Human IgK sequences were likewise searched for comparison to the murine VL domain using BLAST search algorithms, and candidate human variable domains selected from the top 200 BLAST results. These were reduced to four candidates based on a combination of framework homology, maintaining key framework residues and canonical loop structure.
  • the closest human germline IGKV1-27 was selected.
  • the CDRs of the murine VH and VL were then grafted into these acceptor frameworks to yield the 5 humanized VH variants VH1-VH5 (SEQ ID NO:s 13-17) and the 5 humanized VL variants VL1-VL5 (SEQ ID NO:S 18-22).
  • variable domain of a humanized chain has a V region amino acid sequence which, analysed as a whole, is closer to human than to other species (assessed using the Immunogenetics Information System® (IMGT®) DomainGapAlign tool).
  • IMGT® Immunogenetics Information System
  • VL and VH regions were analysed for good candidates for framework back mutations in order to improve the affinity of the humanized antibody to its target.
  • L44 (L) was identified as being unusual in this position (frequency of less than 1%). This position has been shown to be important in the VL/VH interface. In the likely parental germline this position is a valine. Most frequently this position is a proline. This was considered a good candidate for back mutation.
  • the previous amino, L43 (T) was also considered worth keeping as a framework back mutation, although it was noted that one of the 5 humanized sequences also had this sequence. In the closest human germline sequences this was identified as an alanine or valine. Likewise L42 (G) was also considered a good position for a framework back mutation.
  • H43 amino acid at H43 (S) was considered a good candidate for framework back mutation, as it is an important residue in the VH/VL interface, and since this position typically is lysine, glutamine or arginine.
  • H40 (F) and H44 (K) were also considered good positions for framework back mutations as they had a frequency of 1%. Although they were not considered strictly at a key defined position, they are immediately adjacent and thus considered good candidates.
  • the analysis was performed using a Biacore T200 instrument, at 25° C. analysis temperature, at a flow rate of 50 ⁇ l/min for quantitative kinetic interaction analyses.
  • CM4 sensor chip #2
  • VH heavy chain variable regions
  • Each antibody also comprised one the following light chain variable regions (VL):
  • 6B12 Mouse monoclonal IgG1 anti-S100A4 as described in Example 1
  • VH0 VL0 The VH and VL regions of 6B12 comprised in a humanized IgG4 isotype framework.
  • the 14 tested antibodies all had similar dissociation constants to the 6B12 antibody, showing high binding affinities to S100A4.
  • some of the specific framework back-mutations in the humanized light or heavy chains had an improved effect on the dissociation constant.
  • VH1 VL3 showed a K d of 3.47 E-09, while this was improved to 2.25 E-09 for VH1 VL3 L44Leu and to 1.99 E-09 for VH1 VL3_L42Gly+L44Leu.
  • Some of these manually designed framework back mutations thus successfully increased the affinities of the antibody to S100A4.
  • Example 3 Humanized Anti-S100A4 Antibody Efficacy in Treating Bleomycin-Induced Dermal Fibrosis In Vivo
  • SSc Systemic sclerosis
  • SSc Systemic sclerosis
  • SSc is a systemic fibrosing orphan disease with high morbidity and mortality.
  • SSc is the condition with the highest case specific mortality of any of the autoimmune rheumatic diseases with more than half of cases diagnosed with the condition eventually dying as a direct consequence.
  • the hallmark of the disease is accumulation of extracellular matrix proteins by pathologically activated fibroblasts.
  • Therapeutic approaches to selectively inhibit the aberrant release of extracellular matrix in SSc are not available to date.
  • Bleomycin-induced dermal fibrosis is the most commonly used mouse model of SSc. It resembles in particular early, inflammatory stages of SSc.
  • AX-202 a humanized IgG4 mono-clonal anti-S100A4 antibody, was used for this study.
  • the antibody comprises a heavy chain sequence as defined in SEQ ID NO: 58 and a light chain sequence as defined in SEQ ID NO: 59.
  • the antibody was dissolved in PBS and stored at ⁇ 20° C.
  • mice were treated with 057131/6 mice.
  • Skin fibrosis was induced by daily subcutaneous injections of bleomycin (2.5 mg/kg, Sigma-Aldrich) in defined and marked areas of the upper back (1 cm 2 ) for up to six weeks. Treatment was commenced after three weeks of pre-challenge with bleomycin, with injections twice weekly intraperitoneally (i.p.) or once every week with intravenous (IV) injection in the tail vein. The outcome was analysed three weeks after the first injection of bleomycin (six weeks after the first bleomycin-injection).
  • mice were monitored clinically on a daily basis for behavior, activity, texture of the fur and consistency of the stool. After sacrifice, a gross macroscopic evaluation of the lungs and the skin was performed.
  • Myofibroblasts are characterized by the expression of a-smooth muscle actin ( ⁇ SMA). Fibroblasts positive for ⁇ SMA were detected in paraffin-embedded slides from the upper back by incubation with monoclonal anti- ⁇ SMA antibodies (clone 1A4, Sigma-Aldrich, Steinheim, Germany). The expression was visualized with horseradish peroxidase-labelled secondary antibodies and 3,3-diaminobenzidine tetrahydrochloride (DAB) (Sigma-Aldrich). Monoclonal mouse IgG antibodies (Calbiochem, San Diego, CA, USA) were used for controls. The analysis was performed by a blinded reviewer evaluating the myofibroblasts in four sections per sample.
  • DAB 3,3-diaminobenzidine tetrahydrochloride
  • mice developed prominent dermal fibrosis upon challenge with bleomycin with more pronounced fibrotic changes in mice challenged with bleomycin for 6 weeks as compared to mice challenged with bleomycin for 3 weeks followed by injections of the solvent of bleomycin, NaCl, for another 3 weeks. Mice injected with NaCl for 6 weeks served as controls.
  • AX-202 significantly reduced dermal thickening, myofibroblast counts and the hydroxyproline content as compared to control mice injected with bleomycin for 6 weeks (see FIG. 1 ).
  • the effects were dose-dependent with most pronounced effects observed in doses of 16 mg/kg IP and 24 mg/kg once weekly IV (see FIGS. 1 A-C ).
  • FIGS. 1 A-C statistically significant effects of AX-202 were also observed with 8 mg/kg IP every third day.
  • AX-202 also induced regression of fibrosis with statistically significant changes of dermal thickness and myofibroblast counts as compared to mice injected with bleomycin only for three weeks.
  • PBMCs Peripheral blood mononuclear cells
  • Monocytes were plated (100,000 cells/well) into 96 well plates and cultured for 6 hours in the presence of:
  • 6B12 mouse monoclonal IgG1 anti-S100A4 antibody as described in Example 1
  • AX-202 humanized monoclonal IgG4 anti-S100A4 antibody as described in Example 3
  • cytokines IL-6, TNF- ⁇ and IL-10
  • Luminex assay according to manufacturer's instructions (R&D systems; LXSAHM-03).
  • S100A4 evoked an increase in the levels of IL-6, TNF ⁇ and IL-10 (see FIGS. 2 - 4 ).
  • S100A4-evoked IL-6 and IL-10 release was reduced by both AX-202 and 6B12 (see FIGS. 2 C-D and 3 C-D).
  • mouse IgG1 control, human IgG4 control, or AX-202 in combination with S100A4 did not result in significant increases in TNF ⁇ levels compared to S100A4 alone (see FIGS. 4 A-B ).
  • the levels of S100A4-induced pro-inflammatory cytokine TNF ⁇ were increased by treatment with the 6B12 antibody in a dose-dependent fashion (see FIGS. 4 C and 4 D ).
  • the humanized anti-S100A4 IgG4 antibody does not increase S100A4-induced pro-inflammatory TNF ⁇ levels compared to the mouse anti-S100A4 antibody 6B12.
  • Example 5 Humanized Anti-S100A4 Antibodies Show No Cross-Reactivity to Other S100-Family Members and are Specific to S100A4 from Multiple Species
  • VH1_40Phe:VL3, VH1:VL3_Leu44, and VH1_40Phe:VL3_Leu44 was tested by Western blot. All variants detected mouse and human S100A4 protein and did not cross-react with other S100 family members (see FIG. 5 ).
  • AX-202 as described in Example 3, was additionally shown to bind with similar affinity to S100A4 across 4 different species (monkey, rat, human and mouse).
  • Example 6 Humanized Anti-S100A4 Antibody Reduces S100A4-Induced Inflammatory Pathway Activation
  • HEK-Blue hTLR4 (InvivoGen, #hkb-htlr4) cells were incubated in HEK-Blue Detection medium (InvivoGen, #hb-det2) and stimulated with increasing concentration of recombinant human S100A4 multimer or 1.25 ng/ml LPS-EK ultrapure (positive control; InvivoGen, #tlrl-peklps). After 20h incubation, the levels of NF-kB induced secreted embryonic alkaline phosphatase (SEAP) were determined by reading the OD at 620 nm. S100A4 was shown to clearly activate the NF-kB reporter gene in HEKBlue hTLR4 cells in a concentration-dependent manner (see FIG. 7 A ).
  • SEAP NF-kB induced secreted embryonic alkaline phosphatase
  • HEK-Blue hTLR4 and HEK-Blue Null2 (control, InvivoGen, #hkb-null2) cells were incubated in HEK-Blue Detection medium and stimulated either with 1.25 ng/ml LPS-EK ultrapure (InvivoGen, #tlrl-peklps), 1.25 or 2.5 ⁇ g/ml S100A4.
  • Cells treated with 50 ng/ml TNF- ⁇ (InvivoGen, #rcyc-htnfa) were used as a positive control for HEK-Blue Null2 cells activation.
  • S100A4 activation of the NF-kB reporter gene was shown to be dependent on the TLR4, as activation of the reporter gene was completely abrogated in Null2 cells even with addition of S100A4 (see FIG. 7 B ).
  • HEK-Blue hTLR4 cells were incubated in HEK-Blue Detection medium and stimulated with 1.25 ⁇ g/ml S100A4 alone and increasing concentrations of the S100A4-neutralizing antibody AX-202 (described in Example 3). LPS activation of the reporter gene was not affected by AX-202, however AX-202 was shown to inhibit S100A4-induced TLR4 activation in a concentration-dependent manner (see FIG. 7 C ).
  • Fc ⁇ RIIa is an activating Fc ⁇ R with a low affinity for single ‘monomeric’ IgG molecules but high avidity for IgG-containing ICs (Arman et al., 2015).
  • Fc ⁇ RIIA engagement initiates strong effector functions that are key for immune and inflammatory responses, including cytokine release and ADCC (antibody-dependent cellular cytotoxicity), which could negatively influence the safety profile of the antibody-drug.
  • ADCC antibody-dependent cellular cytotoxicity
  • the Fc ⁇ RIIa plays a role in heparin-induced thrombocytopenia, a well-documented prothrombotic adverse drug effect (Sun et al., 2013).
  • This study aims to investigate whether the subclass shift from mouse IgG1 of the parental 6B12 antibody to human IgG4 of AX-202 affects binding affinity towards the Fc ⁇ RIIa.
  • a lower Fc ⁇ RIIA binding affinity of antibody-immune complexes could indicate a better safety profile.
  • IgG-Class Switch from Human IgG1 to IgG4 Substantially Reduces Antigen-Specific Fc ⁇ RIIa Activation
  • the Fc ⁇ RIIa-H ADCP Reporter Bioassay from Promega was employed to measure the antibody subtype difference in potency of Ab-Ag complexes to activate Fc ⁇ RIIa.
  • the assay consists of human Jurkat cells stably expressing human Fc ⁇ RIIa-H (the high-affinity H131 variant) and NFAT-induced luciferase.
  • This study included two different AX-202 antibodies carrying either hlgG from class 1 or 4.
  • the parental mouse antibody, 6B12 IgG1 was included in the study. The results are depicted in FIG. 8 .
  • the immune complexes (ICs) were formed by mixing antibodies with either dimeric (A) or multimer S100A4 protein (B).
  • the receptor clustering is significantly higher for AX-202 hIgG1 compared to AX-202 hIgG4 with a receptor activation fold difference of 5.00 and 3.83 for S100A4-D and S100A4-M, respectively (see FIG. 8 ).
  • 6B12 which has a mouse IgG1 scaffold, has lower potency to induce IC-dependent Fc ⁇ RIIa than its human counterpart (AX-202 hIgG1). However, 6B12 showed still 3.23 (Dimer) and 2.87-fold (Multimer) higher activation than AX-202 hIgG4.
  • Neither IgG1 nor IgG4 control antibodies mediate receptor clustering indicating that Ab-Ag IC formation is important for Fc ⁇ RIIa clustering and activation.
  • Antibodies have recently been found to mediate inflammation and immune modulation by inducing cellular differentiation, activation, and cytokine release (A van Erp et al., 2019). This could lead to unwanted proinflammatory pathway activation and counteract the mode-of-action of the therapeutic S100A4 antibody.
  • an S100A4 neutralizing antibody with an IgG4 scaffold had a much better safety profile than the same antibody with a human IgG1 scaffold, with an approximately 3-fold lower potency to induce Fc ⁇ R activation.
  • CDR-H1 (amino acid Artificial NDYYWN sequence-identified sequence using the Kabat numbering system) 2 CDR-H2 (amino acid Artificial HIGYGGNINYNPSLKN sequence-identified sequence using the Kabat numbering system) 3 CDR-H3 (amino acid Artificial ESFYDGYPFDY sequence-identified sequence using the Kabat numbering system) 4 CDR-H1 (amino acid Artificial GDSFTNDYY sequence-identified sequence using the IMGT numbering system) 5 CDR-H2 (amino acid Artificial IGYGGNI sequence-identified sequence using the IMGT numbering system) 6 CDR-H3 (amino acid Artificial TRESFYDGYPFDY sequence-identified sequence using the IMGT numbering system) 7 CDR-L1 (amino acid Artificial RASQDIRNYLN sequence-identified sequence using the Kabat numbering system) 8 CDR-L2 (amino acid Artificial YTSRLHS sequence-

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