Lakey E K, Margoliash E, Fitch F W, Pierce S K
J Immunol. 1986 Jun 1;136(11):3933-8.
The activation of helper T lymphocytes has been proposed to result from the sum of low-affinity interactions between the specific immune receptor, as well as nonpolymorphic receptors such as L3T4 on the T cell surface, and nominal antigen and Ia displayed in a multivalent array on the antigen-presenting cell surface. The present work takes advantage of a T cell hybridoma specific for pigeon cytochrome c in the context of I-Ek, which responds to tobacco hornworm moth cytochrome c at one hundredth the concentration of the homologous antigen, to determine if the T cell's requirement for L3T4 and Ia is directly related to its functional affinity for antigen. The results demonstrate that the T cell's activation by pigeon cytochrome c was blocked by antibodies directed to L3T4 and to I-Ek, even at antigen concentrations twofold to fourfold above those required for maximal responses. In contrast, the response to tobacco hornworm moth cytochrome c was not as affected by these antibodies under equivalent superoptimal conditions. The same phenomenon was observed for the T cell's activation by the carboxyl-terminal peptide fragments of the two cytochromes c, which do not require processing, indicating that the differences were not due to the relative efficiency of processing and/or presentation of the antigens. Although both I-Ek- and L3T4-specific antibodies blocked the T cell response to pigeon cytochrome, antibodies to I-Ak had no effect, even though I-Ak had been considered to be a ligand for L3T4. Thus, either Ia does not bind L3T4 or, if it does, I-Ek must be a sufficient ligand for L3T4 for T cells that recognize their antigen in the context of I-Ek. These studies provide more definitive evidence that the T cell's requirement for the functions of Ia and of L3T4 is dependent on the T cell's functional affinity for its antigenic determinant. This data is consistent with a model of T cell activation in which, given a high enough affinity of the T cell receptor for the processed antigen, the requirement for other components of a stimulatory complex, such as Ia and L3T4, may diminish to undetectable levels.
辅助性T淋巴细胞的激活被认为是由特异性免疫受体以及T细胞表面的非多态性受体(如L3T4)与抗原呈递细胞表面以多价形式展示的名义抗原和Ia之间低亲和力相互作用的总和所导致。本研究利用了一种在I-Ek背景下对鸽细胞色素c特异的T细胞杂交瘤,该杂交瘤对烟草天蛾细胞色素c的反应浓度是同源抗原的百分之一,以确定T细胞对L3T4和Ia的需求是否与其对抗原的功能亲和力直接相关。结果表明,即使在抗原浓度比最大反应所需浓度高两倍至四倍的情况下,针对L3T4和I-Ek的抗体也能阻断鸽细胞色素c对T细胞的激活。相比之下,在同等超最佳条件下,对烟草天蛾细胞色素c的反应受这些抗体的影响较小。对于两种细胞色素c的羧基末端肽片段激活T细胞的情况也观察到了相同的现象,这些片段不需要加工,这表明差异并非由于抗原加工和/或呈递的相对效率。尽管针对I-Ek和L3T4的特异性抗体都阻断了T细胞对鸽细胞色素的反应,但针对I-Ak的抗体却没有作用,尽管I-Ak曾被认为是L3T4的配体。因此,要么Ia不与L3T4结合,要么如果结合,对于在I-Ek背景下识别其抗原的T细胞来说,I-Ek必须是L3T4的充分配体。这些研究提供了更确凿的证据,表明T细胞对Ia和L3T4功能的需求取决于T细胞对其抗原决定簇的功能亲和力。该数据与T细胞激活模型一致,在该模型中,如果T细胞受体对加工后的抗原具有足够高的亲和力,对刺激复合物其他成分(如Ia和L3T4)的需求可能会降低到检测不到的水平。