Moser G, Burakoff S J, Abbas A K
J Immunol. 1982 Jul;129(1):63-9.
Cytolytic T lymphocytes (CTL) specific for 2,4,6-trinitrophenyl (TNP) determinants suppress the effector phase of a secondary anti-TNP antibody responses of murine syngeneic spleen cells in vitro. The cells mediating this suppression are hapten-specific, H-2-restricted, and possess properties typical of CTL. Moreover, the targets of the suppression appear to be antigen-primed B lymphocytes that are recognized by CTL via soluble antigen bound noncovalently to their Ig receptors. The effect of the CTL can be blocked by the addition of monoclonal antibodies directed against I-A molecules but not I-E or H-EK-encoded molecules on the target B cells, even in strain combinations in which the CTL-B cell interaction is restricted only by the H-2K and I regions of the MHC. This result suggests that B lymphocyte-bound antigen tends to associate preferentially with I-A rather than H-2K/D-encoded determinants, and that the suppressive effect of the CTL population is attributable to the minor subset that recognizes hapten-modified Ia antigens. These findings are also discussed in terms of the possible immunoregulatory function of Ia-restricted CTL.
对2,4,6-三硝基苯基(TNP)决定簇具有特异性的溶细胞性T淋巴细胞(CTL)在体外可抑制小鼠同基因脾细胞二次抗TNP抗体应答的效应阶段。介导这种抑制作用的细胞具有半抗原特异性、H-2限制性,且具备CTL的典型特性。此外,抑制作用的靶细胞似乎是抗原致敏的B淋巴细胞,CTL通过非共价结合于其Ig受体的可溶性抗原识别这些B淋巴细胞。即使在CTL与B细胞相互作用仅受主要组织相容性复合体(MHC)的H-2K和I区限制的品系组合中,加入针对靶B细胞上I-A分子而非I-E或H-EK编码分子的单克隆抗体也可阻断CTL的作用。这一结果表明,B淋巴细胞结合的抗原倾向于优先与I-A而非H-2K/D编码的决定簇结合,并且CTL群体的抑制作用归因于识别半抗原修饰的Ia抗原的较小亚群。还从Ia限制性CTL可能的免疫调节功能方面对这些发现进行了讨论。