Baxevanis C N, Nagy Z A, Klein J
J Immunol. 1983 Aug;131(2):628-32.
Purified Lyt-1+2+ T cells were depleted of alloreactive cells by BUdR and light treatment, and then were primed in vitro against LDHB presented on allogeneic APC. Such cells could be restimulated by LDHB on the same allogeneic APC, but not by LDHB on APC syngeneic with the T cells. The restimulated T cells suppressed the proliferative response of Lyt-1+2- T cells primed and restimulated by the same antigen. The suppression, which was antigen specific, occurred after a 6-hr co-culture of the suppressor (Tse) and proliferating helper (Th) cells. The successful interaction (as measured by suppression) between allogeneic Th and Tse cells was found to be determined by the restriction specificity but not the MHC haplotype of Th cells, and the MHC haplotype but not the restriction specificity of Tse cells. Thus, suppression occurred only when the Tse cells carried genes controlling the MHC molecules that served as restriction elements for antigen recognition by the Th cells. No evidence could be obtained for the participation of APC in the Tse-Th interaction. The data suggest the interaction is based on the recognition by the Th cell of the antigen presented in the context of MHC molecules controlled by the Tse cell.
纯化的Lyt-1+2+ T细胞通过溴脱氧尿苷(BUdR)和光照处理去除同种异体反应性细胞,然后在体外针对同种异体抗原呈递细胞(APC)上呈现的乳酸脱氢酶B(LDHB)进行致敏。此类细胞可被同一同种异体APC上的LDHB再次刺激,但不能被与T细胞同基因的APC上的LDHB刺激。再次刺激的T细胞抑制了由相同抗原致敏和再次刺激的Lyt-1+2- T细胞的增殖反应。这种抑制是抗原特异性的,发生在抑制性(Tse)细胞和增殖性辅助(Th)细胞共培养6小时后。发现同种异体Th细胞和Tse细胞之间的成功相互作用(通过抑制来衡量)取决于Th细胞的限制特异性而非MHC单倍型,以及Tse细胞的MHC单倍型而非限制特异性。因此,只有当Tse细胞携带控制作为Th细胞抗原识别限制元件的MHC分子的基因时,才会发生抑制。没有证据表明APC参与了Tse-Th相互作用。数据表明,这种相互作用基于Th细胞对Tse细胞控制的MHC分子背景下呈现的抗原的识别。