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小鼠抗独特型单克隆抗体MK2-23模拟人高分子量黑色素瘤相关抗原。抗抗独特型单克隆抗体与手术切除的黑色素瘤病灶反应性的免疫组织化学分析。

Human high molecular weight-melanoma associated antigen mimicry by mouse anti-idiotypic MAb MK2-23. Immunohistochemical analysis of the reactivity of anti-anti-idiotypic MAb with surgically removed melanoma lesions.

作者信息

Kageshita T, Hirai S, Ono T, Ferrone S

机构信息

Department of Dermatology, Kumamoto University School of Medicine, Japan.

出版信息

Int J Cancer. 1995 Jan 27;60(3):334-40. doi: 10.1002/ijc.2910600310.

DOI:10.1002/ijc.2910600310
PMID:7829240
Abstract

The mouse anti-id MAb MK2-23 bears the internal image of the antigenic determinant defined by anti-HMW-MAA MAb 763.74. Active specific immunotherapy with anti-id MAb MK2-23 is associated with a statistically significant prolongation of survival in patients with malignant melanoma. Characterization of the immune response elicited by anti-id MAb MK2-23 may contribute to our understanding of the mechanisms underlying the apparent beneficial clinical effects of active specific immunotherapy with anti-id MAb MK2-23. Therefore, 8 HMW-MAA binding anti-anti-id MAbs elicited with MAb MK2-23 were characterized in their reactivity with a large panel of surgically removed benign and malignant tumors and of normal tissues. The 8 anti-anti-id MAbs displayed subtle differences in their immunoperoxidase staining of both benign and malignant lesions and of normal tissues. The diversity in the fine specificity of the 8 anti-anti-id MAbs is likely to reflect the few somatic mutations which occur in the amino-acid sequence of the variable regions of their heavy and light chains in the course of the immune response to MAb MK2-23. The reactivity patterns of the 8 anti-anti-id MAbs with the tissue substrates are similar, although not superimposable upon that of anti-HMW-MAA MAb 763.74 elicited with melanoma cells. This difference may reflect the imperfect mimicry by anti-id MAb MK2-23 of the antigenic determinant defined by anti-HMW-MAA MAb 763.74.

摘要

小鼠抗独特型单克隆抗体MK2-23具有由抗高分子量黑色素瘤相关抗原(HMW-MAA)单克隆抗体763.74所定义的抗原决定簇的内影像。用抗独特型单克隆抗体MK2-23进行主动特异性免疫治疗与恶性黑色素瘤患者生存期的统计学显著延长相关。对抗独特型单克隆抗体MK2-23引发的免疫反应进行表征,可能有助于我们理解用抗独特型单克隆抗体MK2-23进行主动特异性免疫治疗所产生明显有益临床效果的潜在机制。因此,对用单克隆抗体MK2-23引发的8种HMW-MAA结合抗抗独特型单克隆抗体与大量手术切除的良性和恶性肿瘤以及正常组织的反应性进行了表征。这8种抗抗独特型单克隆抗体在对良性和恶性病变以及正常组织的免疫过氧化物酶染色中表现出细微差异。这8种抗抗独特型单克隆抗体精细特异性的多样性可能反映了在对单克隆抗体MK2-23的免疫反应过程中,其重链和轻链可变区氨基酸序列中发生的少数体细胞突变。这8种抗抗独特型单克隆抗体与组织底物的反应模式相似,尽管与用黑色素瘤细胞引发的抗HMW-MAA单克隆抗体763.74的反应模式并不完全重叠。这种差异可能反映了抗独特型单克隆抗体MK2-23对由抗HMW-MAA单克隆抗体763.74所定义的抗原决定簇的模拟并不完美。

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