Kasahara M, Ikeda H, Ogasawara K, Ishikawa N, Okuyama T, Fukasawa Y, Kojima H, Kunikane H, Hawkin S, Ohhashi T
Immunology. 1984 Sep;53(1):79-86.
Recent studies using rabbit antisera to the separated HLA-DR alpha and beta subunits have suggested that alpha chain-specific, but not beta chain-specific, antisera inhibit T cell proliferative responses in primary and secondary human autologous mixed lymphocyte reaction (AMLR). In the present study, with the aid of sequential co-precipitation assays and Western blotting methods, a monoclonal rat alloantibody 1E4, specific for the beta chain of rat class II molecules carrying an Ia determinant Ba-2.7, was characterized to recognize a monomorphic determinant located on the beta chain of DR antigens. This antibody and a murine monoclonal antibody HU-4, also specific for the beta chain of DR antigens, strongly inhibited both primary and secondary AMLR through a mechanism distinct from an antibody-dependent cell-mediated cytotoxicity reaction. These results indicate that the inhibition of AMLR is not a unique feature of DR alpha-specific antibodies.
最近使用针对分离的HLA - DRα和β亚基的兔抗血清进行的研究表明,α链特异性抗血清而非β链特异性抗血清可抑制原发性和继发性人类自体混合淋巴细胞反应(AMLR)中的T细胞增殖反应。在本研究中,借助于连续共沉淀分析和蛋白质印迹法,对一种针对携带Ia决定簇Ba - 2.7的大鼠Ⅱ类分子β链的单克隆大鼠同种异体抗体1E4进行了鉴定,发现它可识别位于DR抗原β链上的一个单态决定簇。该抗体以及同样针对DR抗原β链的鼠单克隆抗体HU - 4,通过一种不同于抗体依赖性细胞介导的细胞毒性反应的机制,强烈抑制原发性和继发性AMLR。这些结果表明,抑制AMLR并非DRα特异性抗体的独特特性。