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一种识别封装在可生物降解微球中的卵巢癌抗原CA125的鼠单克隆抗体诱导抗独特型体液免疫和细胞免疫反应。

Induction of anti-idiotypic humoral and cellular immune responses by a murine monoclonal antibody recognizing the ovarian carcinoma antigen CA125 encapsulated in biodegradable microspheres.

作者信息

Ma J, Samuel J, Kwon G S, Noujaim A A, Madiyalakan R

机构信息

Research and Development, AltaRex Corp., Edmonton, Alberta, Canada.

出版信息

Cancer Immunol Immunother. 1998 Sep;47(1):13-20. doi: 10.1007/s002620050499.

Abstract

The use of biodegradable poly(DL-lactic-co-glycolic acid) microspheres as a cancer vaccine delivery system for induction of anti-idiotypic responses was investigated using a murine monoclonal antibody B43.13 that recognizes the human ovarian cancer antigen CA125. Immunization of mice with mAb B43.13 encapsulated in poly(DL-lactic-co-glycolic acid) microspheres resulted in enhanced humoral and cellular immune responses compared with mAb B43.13 alone or mAb B43.13 mixed with microspheres. The antibody responses could be further enhanced by the co-encapsulation of mAb B43.13 with monophosphoryl lipid A, a non-toxic adjuvant, in microspheres. Anti-idiotypic humoral responses were shown to result in Ab2 antibodies mimicking the nominal antigen CA125 and Ab3 antibodies recognizing CA125. Further, microsphere delivery of mAb B43.13 also resulted in induction of T cell responses involving T2 cells reactive with mAb B43.13 epitopes and T3 cells recognizing CA125. These results indicate that microsphere delivery of Abl can induce both humoral and cellular anti-idiotypic responses relevant to cancer antigens. This raises the possibility of the use of such formulations for anti-idiotypic induction immunotherapy for cancer.

摘要

利用识别人类卵巢癌抗原CA125的鼠单克隆抗体B43.13,研究了可生物降解的聚(DL-乳酸-乙醇酸共聚物)微球作为癌症疫苗递送系统诱导抗独特型反应的作用。与单独的单克隆抗体B43.13或与微球混合的单克隆抗体B43.13相比,用包裹在聚(DL-乳酸-乙醇酸共聚物)微球中的单克隆抗体B43.13免疫小鼠可增强体液免疫和细胞免疫反应。通过在微球中共包裹单克隆抗体B43.13和无毒佐剂单磷酰脂质A,抗体反应可进一步增强。抗独特型体液反应显示可产生模拟标称抗原CA125的Ab2抗体和识别CA125的Ab3抗体。此外,单克隆抗体B43.13的微球递送还导致诱导T细胞反应,涉及与单克隆抗体B43.13表位反应的T2细胞和识别CA125的T3细胞。这些结果表明,Abl的微球递送可诱导与癌症抗原相关的体液和细胞抗独特型反应。这增加了使用此类制剂进行癌症抗独特型诱导免疫治疗的可能性。

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