2009 Fiscal Year Final Research Report
Adoptive immunotherapy using bispecific antibody that blocks theEGFR signaling pathway
Project/Area Number |
19790934
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Digestive surgery
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Research Institution | Tohoku University |
Principal Investigator |
HIROKI Hayashi Tohoku University, 病院, 助教 (30422124)
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Project Period (FY) |
2007 – 2009
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Keywords | 二重特異性抗体 / 上皮増殖因子受容体 / EGFR / 養子免疫療法 |
Research Abstract |
We develop the bispecific antibody that binds both epidermal growth factor receptor (EGFR) and CD3 (lymphocyte's cell surface marker). This bispecific antibody greatly enhances lymphocyte's killer activity against cancer cells when administrated with lymphocytes. This effect is only observed against EGFR positive cancer cells (not against EGFR negative cells). This bispecific antibody seems very promising molecules against cancer immunotherapy because EGFR is widely expressing in many type of solid cancer. This effect was also observed in therapeutic models using mice.
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[Journal Article] Application of the Fc fusion format to generate tag-free bi-specific diabodies.2010
Author(s)
Asano R, Ikoma K, Kawaguchi H, Ishiyama Y, Nakanishi T, Umetsu M, Hayashi H, Katayose Y, Unno M, Kudo T, Kumagai I
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Journal Title
FEBS J 277(2)
Pages: 477-87
Peer Reviewed
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[Journal Article] Highly effective recombinant format of a humanized IgG-like bispecific antibody for cancer immunotherapy with retargeting of lymphocytes to tumor cells.2007
Author(s)
Asano R, Watanabe Y, Kawaguchi H, Fukazawa H, Nakanishi T, Umetsu M, Hayashi H, Katayose Y, Unno M, Kudo T, Kumagai I
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Journal Title
J Biol Chem 282(38)
Pages: 27659-65
Peer Reviewed
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