Humanizing murine IgG3 anti-GD2 antibody m3F8 substantially improves antibody-dependent cell-mediated cytotoxicity while retaining targeting in vivo
| Autor: | Jian Hu, Irene Y. Cheung, Nai-Kong V. Cheung, Hong-fen Guo, Dimiter V. Tassev |
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| Rok vydání: | 2012 |
| Předmět: |
Immunology
chemical and pharmacologic phenomena antibody-dependent cell-mediated cytotoxicity (ADCC) Peripheral blood mononuclear cell complement mediated cytotoxicity (CMC) Affinity chromatography In vivo Immunology and Allergy Medicine monoclonal antibodies (MoAb) Cytotoxicity Antibody-dependent cell-mediated cytotoxicity humanized biology business.industry polymorphonuclear leukocytes (PMN) Molecular biology In vitro chimeric Oncology biology.protein peripheral blood mononuclear cells (PBMC) Antibody Protein A business Research Paper |
| Zdroj: | Oncoimmunology |
| ISSN: | 2162-402X |
| DOI: | 10.4161/onci.19864 |
| Popis: | Murine IgG3 anti-GD2 antibody m3F8 has shown anti-neuroblastoma activity in Phase I/II studies, where antibody-dependent cell-mediated cytotoxicity (ADCC) played a key role. Humanization of m3F8 should circumvent human anti-mouse antibody (HAMA) response and enhance its ADCC properties to reduce dosing and pain side effect. Chimeric 3F8 (ch3F8) and humanized 3F8 (hu3F8-IgG1 and hu3F8-IgG4) were produced and purified by protein A affinity chromatography. In vitro comparison was made with m3F8 and other anti-GD2 antibodies in binding, cytotoxicity, and cross-reactivity assays. In GD2 binding studies by SPR, ch3F8 and hu3F8 maintained K(D) comparable to m3F8. Unlike other anti-GD2 antibodies, m3F8, ch3F8 and hu3F8 had substantially slower k(off.). Similar to m3F8, both ch3F8 and hu3F8 inhibited tumor cell growth in vitro, while cross-reactivity with other gangliosides was comparable to that of m3F8. Both peripheral blood mononuclear cell (PBMC)-ADCC and polymorphonuclear leukocytes (PMN)-ADCC of ch3F8 and hu3F8-IgG1 were more potent than m3F8. This superiority was consistently observed in ADCC assays, irrespective of donors or NK-92MI-transfected human CD16 or CD32, whereas complement mediated cytotoxicity (CMC) was reduced. As expected, hu3F8-IgG4 had near absent PBMC-ADCC and CMC. Hu3F8 and m3F8 had similar tumor-to-non tumor ratios in biodistribution studies. Anti-tumor effect against neuroblastoma xenografts was better with hu3F8-IgG1 than m3F8. In conclusion, humanizing m3F8 produced next generation anti-GD2 antibodies with substantially more potent ADCC in vitro and anti-tumor activity in vivo. By leveraging ADCC over CMC, they may be clinically more effective, while minimizing pain and HAMA side effects. A Phase I trial using hu3F8-IgG1 is ongoing. |
| Databáze: | OpenAIRE |
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