T Kawamoto, K Kishimoto, K Takahashi, T Matsumura, J D Sato, S Taniguchi
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引用次数: 10
Abstract
The ability of different Fc receptors (Fc gamma R) on IgG-mediated cytotoxicity for human epidermoid carcinoma A431 cells bearing large number of epidermal growth factor receptors (EGFRs) was examined by using two isotypes (IgG1 and IgG2a) of murine monoclonal antibodies (MoAbs) against EGFR in the presence of human monocytes and granulocytes. Two MoAbs (225 and LA1) of the IgG1 isotype exhibited effective cytolytic activity for A431 cells with human polymorphonuclear leukocytes (PMN) rather than with human mononuclear cells (MNC). In contrast, two MoAbs (528 and 579) of the IgG2a-isotype lysed the cells less effectively with PMN than with MNC. Anti-Fc gamma R II (CDw32) MoAb 2E1 inhibited the IgG1-mediated cytotoxicity by PMN, and anti-Fc gamma R III (CD16) MoAb 80H3 did not inhibit the IgG2a-mediated cytotoxicity by MNC. Under these conditions, antibody-dependent cell-mediated cytotoxicity by mouse MoAb IgG1 isotypes resulted from antibody binding to the Fc gamma R II (CDw32) of PMN.
在人单核细胞和粒细胞存在的情况下,使用抗EGFR的两种同种型(IgG1和IgG2a)小鼠单克隆抗体(MoAbs)检测了不同Fc受体(Fc γ R)对含有大量表皮生长因子受体(EGFR)的人表皮样癌A431细胞igg介导的细胞毒性的能力。IgG1同型的两种moab(225和LA1)对人多形核白细胞(PMN)的A431细胞表现出有效的细胞溶解活性,而不是对人单核细胞(MNC)。相比之下,igg2a同型的两个moab(528和579)在PMN作用下裂解细胞的效果不如在MNC作用下。抗fc γ R II (CDw32) MoAb 2E1抑制PMN介导的igg1介导的细胞毒性,而抗fc γ R III (CD16) MoAb 80H3不抑制MNC介导的igg2a介导的细胞毒性。在这些条件下,抗体依赖细胞介导的小鼠MoAb IgG1同型细胞毒性是由抗体与PMN的Fc γ R II (CDw32)结合引起的。