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用模拟表位肽引发的人高分子量黑色素瘤相关抗原特异性抗体靶向黑色素瘤细胞:功能效应

Targeting melanoma cells with human high molecular weight-melanoma associated antigen-specific antibodies elicited by a peptide mimotope: functional effects.

作者信息

Luo Wei, Ko Eric, Hsu Jeff Chi-feng, Wang Xinhui, Ferrone Soldano

机构信息

Department of Immunology, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263, USA.

出版信息

J Immunol. 2006 May 15;176(10):6046-54. doi: 10.4049/jimmunol.176.10.6046.

Abstract

Human high molecular weight-melanoma associated Ag (HMW-MAA) mimics have been shown to elicit HMW-MAA-specific humoral immune responses that appear to be clinically beneficial. This finding has stimulated interest in characterizing the mechanism(s) underlying the ability of the elicited Abs to exert an anti-tumor effect. To address this question, in the present study, we have generated HMW-MAA-specific Abs by sequentially immunizing rabbits with the peptide P763.74, which mimics the HMW-MAA determinant recognized by mAb 763.74, and with HMW-MAA(+) melanoma cells. HMW-MAA-specific Abs isolated from immunized rabbits mediated cell-dependent cytotoxicity but did not mediate complement-dependent cytotoxicity of HMW-MAA(+) melanoma cells. These Abs also effectively inhibited spreading, migration and Matrigel invasion of HMW-MAA(+) melanoma cells. Besides contributing to our understanding of the role of HMW-MAA in the biology of melanoma cells, these results suggest that both immunological and nonimmunological mechanisms underlie the beneficial clinical effects associated with the induction of HMW-MAA-specific Abs in melanoma patients immunized with a HMW-MAA mimic.

摘要

人高分子量黑色素瘤相关抗原(HMW-MAA)模拟物已被证明能引发HMW-MAA特异性体液免疫反应,这些反应似乎具有临床益处。这一发现激发了人们对确定所诱导抗体发挥抗肿瘤作用的潜在机制的兴趣。为了解决这个问题,在本研究中,我们通过用模拟单克隆抗体763.74识别的HMW-MAA决定簇的肽P763.74以及HMW-MAA(+)黑色素瘤细胞依次免疫兔子,产生了HMW-MAA特异性抗体。从免疫兔子中分离出的HMW-MAA特异性抗体介导细胞依赖性细胞毒性,但不介导HMW-MAA(+)黑色素瘤细胞的补体依赖性细胞毒性。这些抗体还能有效抑制HMW-MAA(+)黑色素瘤细胞的铺展、迁移和基质胶侵袭。除了有助于我们理解HMW-MAA在黑色素瘤细胞生物学中的作用外,这些结果表明,在用HMW-MAA模拟物免疫的黑色素瘤患者中,与诱导HMW-MAA特异性抗体相关的有益临床效果是由免疫和非免疫机制共同作用的结果。

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