Thromb Haemost 2006; 96(05): 671-684
DOI: 10.1160/TH06-06-0297
New Technologies, Diagnostic Tools and Drugs
Schattauer GmbH

Rational humanization of the powerful antithrombotic anti-GPIbα antibody: 6B4

Alexandre Fontayne
1   Laboratory for Thrombosis Research, IRC, KU Leuven Campus Kortrijk, Belgium
,
Karen Vanhoorelbeke
1   Laboratory for Thrombosis Research, IRC, KU Leuven Campus Kortrijk, Belgium
,
Inge Pareyn
1   Laboratory for Thrombosis Research, IRC, KU Leuven Campus Kortrijk, Belgium
,
Isabel Van Rompaey
2   Thromb-X NV, Leuven, Belgium
,
Muriel Meiring
3   Department of Hematology and Cell Biology, Faculty of Health Sciences, University of the Free State, South Africa
,
Seb Lamprecht
3   Department of Hematology and Cell Biology, Faculty of Health Sciences, University of the Free State, South Africa
,
Jan Roodt
3   Department of Hematology and Cell Biology, Faculty of Health Sciences, University of the Free State, South Africa
,
Johan Desmet
4   Algonomics NV, Gent, Belgium
,
Hans Deckmyn
1   Laboratory for Thrombosis Research, IRC, KU Leuven Campus Kortrijk, Belgium
› Author Affiliations
Financial support: This work was supported by a grant from the Instituut voor de Aanmoediging van Innovatie door Wetenschap en Technologie in Vlaanderen (IWT 020473) and by a Bilateral Collaboration grant between Flanders and South Africa (BIL/04/56). A.F. is a EU-RTN postdoctoral fellow and K.V.a postdoctoral fellow of the ‘Fonds voor Wetenschappelijk Onderzoek (FWO) Vlaanderen’ Belgium.
Further Information

Publication History

Received 01 June 2006

Accepted after revision 11 September 2006

Publication Date:
01 December 2017 (online)

Summary

Fab-fragments of the monoclonal antibody 6B4, raised against human glycoprotein Ibα (GPIbα), have a powerful antithrombotic effect in baboons by blocking the GPIbα binding site for von Willebrand factor (VWF), without significant prolongation of the skin bleeding time. In order to bring this antibody to the clinic,we here humanized for the first time an anti-human GPIbα by variable-domain resurfacing guided by computer modeling. First, the genes coding for the variable regions of the heavy and light chains of 6B4 were cloned and sequenced. Based on this,a three-dimensional structure of the Fv-fragment was constructed by using homology-based modeling, and with this and comparison with antibodies with known structure,”murine” putative immunogenic residues which are exposed, were changed for “human-like” residues. The humanized Fab-fragment, h6B4-Fab, was constructed in the pKaneo vector system, expressed and purified and showed in vitro an unaltered, even slightly higher binding affinity for its antigen than the murine form as determined by different ELISA set-ups and surface plasmon resonance. Finally, injection of doses of 0.1 to 1.5 mg/kg of h6B4-Fab in baboons showed that both pharmacokinetics and ex-vivo bio-activity of the molecule were to a large extent preserved.In conclusion, the method used here to humanize 6B4 by resurfacing resulted in a fully active derivative, which is now ready for further development.

 
  • References

  • 1 Kohler G, Milstein C. Continuous cultures of fused cells secreting antibody of predefined specificity. Nature 1975; 256: 495-7.
  • 2 Cauwenberghs N, Vanhoorelbeke K, Vauterin S. et al. Epitope mapping of inhibitory antibodies against platelet glycoprotein Ibalpha reveals interaction between the leucine-rich repeat N-terminal and C-terminal flanking domains of glycoprotein Ibalpha. Blood 2001; 98: 652-60.
  • 3 Cauwenberghs N, Schlammadinger A, Vauterin S. et al. Fc-receptor dependent platelet aggregation induced by monoclonal antibodies against platelet glycoprotein Ib or von Willebrand factor. Thromb Haemost 2001; 85: 679-85.
  • 4 Huizinga EG, Tsuji S, Romijn RA. et al. Structures of glycoprotein Ibalpha and its complex with von Willebrand factor A1 domain. Science 2002; 297: 1176-9.
  • 5 Uff S, Clemetson JM, Harrison T. et al. Crystal structure of the platelet glycoprotein Ibalpha N-terminal domain reveals an unmasking mechanism for receptor activation. J Biol Chem 2002; 277: 35657-63.
  • 6 Cauwenberghs N, Meiring M, Vauterin S. et al. Antithrombotic effect of platelet glycoprotein Ibblocking monoclonal antibody Fab fragments in nonhuman primates. Arterioscler Thromb Vasc Biol 2000; 20: 1347-53.
  • 7 Wu D, Meiring M, Kotze HF. et al. Inhibition of platelet glycoprotein Ib, glycoprotein IIb/IIIa, or both by monoclonal antibodies prevents arterial thrombosis in baboons. Arterioscler Thromb Vasc Biol 2002; 22: 323-8.
  • 8 Jaffers GJ, Fuller TC, Cosimi AB. et al. Monoclonal antibody therapy Anti-idiotypic and non-anti-idiotypic antibodies to OKT3 arising despite intense immunosuppression. Transplantation 1986; 41: 572-8.
  • 9 Bruggemann M, Winter G, Waldmann H. et al. The immunogenicity of chimeric antibodies. J Exp Med 1989; 170: 2153-7.
  • 10 Morrison SL, Johnson MJ, Herzenberg LA. et al. Chimeric human-antibody molecules - Mouse antigenbinding domains with human constant region domains. Proc Nat Acad Sci USA 1984; 81: 6851-5.
  • 11 Verhoeyen M, Milstein C, Winter G. Reshaping human antibodies: grafting an antilysozyme activity. Science 1988; 239: 1534-6.
  • 12 Queen C, Schneider WP, Selick HE. et al. A humanized antibody that binds to the interleukin 2 receptor. Proc Natl Acad Sci USA 1989; 86: 10029-33.
  • 13 Padlan EA. A possible procedure for reducing the immunogenicity of antibody variable domains while preserving their ligand-binding properties. Mol Immunol 1991; 28: 489-98.
  • 14 Roguska MA, Pedersen JT, Keddy CA. et al. Humanization of murine monoclonal antibodies through variable domain resurfacing. Proc Natl Acad Sci USA 1994; 91: 969-73.
  • 15 Roguska MA, Pedersen JT, Henry AH. et al. A comparison of two murine monoclonal antibodies humanized by CDR-grafting and variable domain resurfacing. Protein Eng 1996; 09: 895-904.
  • 16 O’Connor SJ, Meng YG, Rezaie AR. et al. Humanization of an antibody against human proteinC and calcium-dependence involving framework residues. Protein Eng 1998; 11: 321-8.
  • 17 Orlandi R, Gussow DH, Jones PT. et al. Cloning immunoglobulin variable domains for expression by the polymerase chain reaction. Proc Natl Acad Sci USA 1989; 86: 3833-7.
  • 18 Staelens S, Desmet J, Ngo TH. et al. Humanization by variable domain resurfacing and grafting on a human IgG4, using a new approach for determination of non-human like surface accessible framework residues based on homology modelling of variable domains. Mol Immunol 2006; 43: 1243-57.
  • 19 Jacquemin M, Benhida A, Peerlinck K. et al. A human antibody directed to the factor VIII C1 domain inhibits factor VIII cofactor activity and binding to von Willebrand factor. Blood 2000; 95: 156-63.
  • 20 Dewerchin M, Van der EL, Singh I. et al. Inhibition of factor VIII witha partially inhibitory human recombinant monoclonal antibody prevents thrombotic events in a transgenic model of type II HBS antithrombin deficiency in mice. J Thromb Haemost 2004; 02: 77-84.
  • 21 Altschul SF, Madden TL, Schaffer AA. et al. Gapped BLAST and PSI-BLAST:a new generation of protein database search programs. Nucleic Acids Res 1997; 25: 3389-402.
  • 22 Delhaise P, Bardiaux M, De Maeyer M. et al. The Brugel Package - Toward Computer-Aided-Design of Macromolecules. J Mol Graphics 1988; 06: 219-23.
  • 23 Desmet J, Spriet J, Lasters I. Fast and accurate sidechain topology and energy refinement (FASTER) as a new method for protein structure optimization. Proteins 2002; 48: 31-43.
  • 24 Vanhoorelbeke K, Pareyn I, Schlammadinger A. et al. Plasma glycocalicin as a source of GPlb alpha in the von Willebrand factor ristocetin cofactor ELISA. Thromb Haemost 2005; 93: 165-71.
  • 25 Dubel S, Breitling F, Fuchs P. et al. Isolation of IgG antibody Fv-DNA from various mouse and rat hybridoma cell lines using the polymerase chain reaction with a simple set of primers. J Immunol Methods 1994; 175: 89-95.
  • 26 Wang Z, Raifu M, Howard M. et al. Universal PCR amplification of mouse immunoglobulin gene variable regions: the design of degenerate primers and an assessment of the effect of DNA polymerase 3’ to 5’ exonuclease activity. J Immunol Methods 2000; 233: 167-77.
  • 27 Kabat EA, Wu TT, Reid-Miller M. et al. Sequences of proteins of immunological interest. 4th Ed. 1987
  • 28 Horton RM, Hunt HD, Ho SN. et al. Engineering hybrid genes without the use of restriction enzymes: gene splicing by overlap extension. Gene 1989; 77: 61-8.
  • 29 Hagay Y, Lahav J, Levanon A. et al. Functionmodulating human monoclonal antibodies against platelet-membrane receptors isolated from a phage-display library. J Thromb Haemost 2003; 01: 1829-36.
  • 30 Ward CM, Andrews RK, Smith AI. et al. Mocarhagin, a novel cobra venom metalloproteinase, cleaves the platelet von Willebrand factor receptor glycoprotein Ibalpha Identification of the sulfated tyrosine/anionic sequence Tyr-276-Glu-282 of glycoprotein Ibalpha as a binding site for von Willebrand factor and alpha-thrombin. Biochemistry 1996; 35: 4929-38.
  • 31 Akiyama M, Takami H, Yoshida Y. The mechanism of cold-induced platelet aggregation in the presence of heparin. Tohoku J Exp Med 1995; 177: 365-74.
  • 32 Cadroy Y, Hanson SR, Kelly AB. et al. Relative antithrombotic effects of monoclonal antibodies targeting different platelet glycoprotein-adhesive molecule interactions in nonhuman primates. Blood 1994; 83: 3218-24.
  • 33 Becker BH, Miller JL. Effects of an antiplatelet glycoprotein Ib antibody on hemostatic function in the guinea pig. Blood 1989; 74: 690-4.
  • 34 Luo D, Mah N, Krantz M. et al. Vl-linker-Vh orientation-dependent expression of single chain Fv-containing an engineered disulfide-stabilized bond in the framework regions. J Biochem (Tokyo) 1995; 118: 825-31.
  • 35 Kim JK, Min W, Lillehoj HS. et al. Generation and characterization of recombinant ScFv antibodies detecting Eimeria acervulina surface antigens. Hybridoma 2001; 20: 175-81.
  • 36 Dai K, An G, Ruan C. Construction and characterization of bispecific single-chain antibody fragments SZ-2/SZ-21 against platelet glycoprotein Ib alpha and beta3. Zhonghua Yi Xue Za Zhi 2002; 82: 1493-7.