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半抗原特异性抑制性T细胞与体外培养的辅助性T细胞系之间的体内相互作用。

Interaction in vivo between hapten-specific suppressor T cells and an in vitro cultured helper T cell line.

作者信息

Owens T, Miller J F

出版信息

J Immunol. 1987 Mar 15;138(6):1687-92.

PMID:2950167
Abstract

The interaction in vivo between hapten-specific suppressor T cells (Ts) and a hapten-specific T helper (Th) cell line was examined. Antigen-specific Ts were induced in CBA mice by i.v. priming with 3 X 10(7) syngeneic spleen cells (SC) that were chemically coupled with the hapten azobenzenearsonate (ABA). Transfer of splenic T cells from these mice by i.v. injection suppressed the induction in syngeneic assay hosts of ABA-reactive helper and cytotoxic T cell (Tc) responses. Although the Th responses and their suppression were ABA specific, in that they were not induced or activated by trinitrophenyl (TNP)-coupled SC, both Tc responses and their suppression were occasionally nonspecific. Induction of Th was assayed by measuring the release from primed lymph node cells of IL 2 and IL 3 in response to haptenated SC in vitro. Both cytotoxic and Th responses could be made dependent on the provision of exogenous Th by reducing the antigen dose. This stratagem allowed the assay in vivo of a long-term cultured ABA-specific Th cell line (E9). Injection of 10(5) E9 cells/mouse (with antigen, in the rear footpad) helped the induction of both Tc and Th in response to a reduced dose of antigen. These responses, which were dependent on the E9 cell line, were also suppressed by i.v. transferred Ts. When normal doses of antigen were used, the injection of 10(5) E9 Th overcame suppression. These results show that Ts act by inhibiting the activation of Th, thereby suppressing Th-dependent responses generally. The fact that the E9 Th cell line could be suppressed also shows that long-term culture of T cells does not affect their capacity to be regulated in vivo.

摘要

对半抗原特异性抑制性T细胞(Ts)与半抗原特异性辅助性T细胞系(Th)在体内的相互作用进行了研究。通过静脉注射用化学偶联了半抗原偶氮苯砷酸盐(ABA)的3×10⁷ 同基因脾细胞(SC),在CBA小鼠中诱导出抗原特异性Ts。通过静脉注射将这些小鼠的脾T细胞转移,可抑制同基因检测宿主中ABA反应性辅助性T细胞和细胞毒性T细胞(Tc)反应的诱导。尽管Th反应及其抑制是ABA特异性的,即它们不会由三硝基苯基(TNP)偶联的SC诱导或激活,但Tc反应及其抑制偶尔是非特异性的。通过测量体外对半抗原化SC反应时,致敏淋巴结细胞释放的IL-2和IL-3来检测Th的诱导情况。通过降低抗原剂量,细胞毒性反应和Th反应都可以依赖于外源性Th的提供。这种策略使得能够在体内对半抗原特异性Th细胞系(E9)进行长期培养的检测。每只小鼠注射10⁵ 个E9细胞(与抗原一起,注射到后足垫)有助于在降低抗原剂量时诱导Tc和Th。这些依赖于E9细胞系的反应也被静脉转移的Ts所抑制。当使用正常剂量的抗原时,注射10⁵ 个E9 Th可克服抑制作用。这些结果表明,Ts通过抑制Th的激活起作用,从而总体上抑制Th依赖性反应。E9 Th细胞系也能被抑制这一事实还表明,T细胞的长期培养并不影响它们在体内被调节的能力。

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