Sondel P M, Bach F H
Tissue Antigens. 1976 Mar;7(3):173-80. doi: 10.1111/j.1399-0039.1976.tb01048.x.
In vitro sensitized cytotoxic T lymphocytes (CTLs) primarily detect antigens controlled within the major histocompatibility complex (MHC) that are associated with the serologically detected (SD) loci LA and FOUR. Frequently CTLs sensitized to cells from one individual kill target cells of a third party that shares no SD cross-reactivities by serological criteria with the initial stimulating cells. We have studied the possibility that this cross-killing is due to the recognition of non-MHC controlled antigens. Allogeneic tissue from MHC identical siblings is rejected in the absence of immunosuppression, demonstrating the importance of non-MHC antigens. Nevertheless, CTLs sensitized simultaneously with mitomycin-C treated cells from an MHC identical sibling and from an unrelated individual were only able to mediate cytotoxicity on the unrelated's target cells. No significant cytotoxicity was observed in any combination on target cells differing only for non-MHC antigens.
体外致敏的细胞毒性T淋巴细胞(CTL)主要检测主要组织相容性复合体(MHC)内控制的抗原,这些抗原与血清学检测到的(SD)位点LA和FOUR相关。通常,对来自一个个体的细胞致敏的CTL会杀死第三方的靶细胞,该第三方与初始刺激细胞在血清学标准上没有SD交叉反应性。我们研究了这种交叉杀伤是否由于对非MHC控制抗原的识别。来自MHC相同同胞的同种异体组织在没有免疫抑制的情况下会被排斥,这证明了非MHC抗原的重要性。然而,与来自MHC相同同胞和无关个体的丝裂霉素-C处理细胞同时致敏的CTL仅能够介导对无关个体靶细胞的细胞毒性。在仅因非MHC抗原不同的靶细胞的任何组合中均未观察到明显的细胞毒性。