Starling G C, Davidson S E, McKenzie J L, Hart D N
Immunology. 1987 Jul;61(3):351-6.
Three monoclonal antibodies recognizing different epitopes of the leucocyte common molecule, CMRF-11 (against the restricted or B-220 leucocyte common molecule), CMRF-12 and CMRF-26 [each against a different epitope on the non-restricted or T200 leucocyte common (CD45) molecule], were tested for their effects on lymphocyte cytotoxicity. The individual monoclonal antibodies inhibited human natural killer cell-mediated cytolysis (NK-CMC) weakly, but a mixture of CMRF-11 + 12 + 26 antibodies inhibited cytolysis more consistently and to a greater extent. This mixture did not inhibit cytotoxic T lymphocytes derived from secondary mixed lymphocyte cultures. The CMRF-11 + 12 + 26 mix was shown to inhibit a post-conjugate formation stage of lysis at the effector cell level. Inhibition of NK-CMC of a wide range of target cells, including the T-cell lines Jurkat, HSB2 and Molt 4, was demonstrated.
三种识别白细胞共同分子不同表位的单克隆抗体,即CMRF-11(针对限制性或B-220白细胞共同分子)、CMRF-12和CMRF-26 [每种针对非限制性或T200白细胞共同(CD45)分子上的不同表位],被检测它们对淋巴细胞细胞毒性的影响。单独的单克隆抗体对人自然杀伤细胞介导的细胞溶解(NK-CMC)有微弱抑制作用,但CMRF-11 + 12 + 26抗体混合物对细胞溶解的抑制作用更稳定且程度更大。该混合物不抑制来自二级混合淋巴细胞培养物的细胞毒性T淋巴细胞。已证明CMRF-11 + 12 + 26混合物在效应细胞水平抑制裂解的共轭后形成阶段。证实了对包括T细胞系Jurkat、HSB2和Molt 4在内的多种靶细胞的NK-CMC有抑制作用。