Butler L D, Miller S D, Claman H N
J Immunol. 1981 Oct;127(4):1383-7.
These experiments concern the regulation of cytotoxic T lymphocytes (CTL). Here we describe the induction of unresponsiveness in TNP-specific cytotoxic cells generated in vitro. Previous work has shown that i.v. injection of water-soluble TNP (TNBS) prevents in vivo generation of TNP-specific CTL in C3H/HeN mice. In contrast, this report shows that the in vitro generation of TNP-specific CTL from similarly treated C3H/HeN mice is not inhibited. Nevertheless, unresponsiveness in CTL can be induced with TNBS. This unresponsiveness appears to be H-2 linked, since 3 strains of H-2d mice (BALB/c, DBA/2J, and B10.D2) were rendered unresponsive after a single injection of TNBS, whereas 3 strains of H-2k mice (C58/J, C3H/HeN, and CBA/J) were not. This CTL unresponsiveness is antigen specific in both induction and expression. The unresponsiveness is reversed by pretreatment with cyclophosphamide but not by adult thymectomy. Furthermore, the addition of supernatants from Con A-stimulated spleen cells to cultures containing the unresponsive responder cells enhanced the generation of cytotoxic activity. These results suggest that a) the ability to induce TNP-specific CTL unresponsiveness is linked to H-2 loci, b) a regulatory network is involved in the unresponsiveness, which is sensitive to cyclophosphamide but resistant to adult thymectomy, and c) at least 1 level of regulation involves amplifying T cells.
这些实验涉及细胞毒性T淋巴细胞(CTL)的调节。在此,我们描述了体外产生的TNP特异性细胞毒性细胞无反应性的诱导过程。先前的研究表明,静脉注射水溶性TNP(TNBS)可阻止C3H/HeN小鼠体内TNP特异性CTL的产生。相比之下,本报告显示,同样处理的C3H/HeN小鼠体外产生TNP特异性CTL并未受到抑制。然而,TNBS可诱导CTL产生无反应性。这种无反应性似乎与H-2相关,因为单次注射TNBS后,3种H-2d小鼠品系(BALB/c、DBA/2J和B10.D2)变得无反应,而3种H-2k小鼠品系(C58/J、C3H/HeN和CBA/J)则没有。这种CTL无反应性在诱导和表达上均具有抗原特异性。用环磷酰胺预处理可逆转无反应性,而成年胸腺切除则不能。此外,将Con A刺激的脾细胞培养上清液添加到含有无反应性应答细胞的培养物中,可增强细胞毒性活性的产生。这些结果表明:a)诱导TNP特异性CTL无反应性的能力与H-2基因座相关;b)一个调节网络参与了无反应性,该网络对环磷酰胺敏感,但对成年胸腺切除有抗性;c)至少有一个调节水平涉及放大T细胞。