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抗原和受体驱动的调节机制。IV. 携带独特型的I-J+抑制性T细胞因子诱导表达抗独特型受体的二级抑制性T细胞。

Antigen- and receptor-driven regulatory mechanisms. IV. Idiotype-bearing I-J+ suppressor T cell factors induce second-order suppressor T cells which express anti-idiotypic receptors.

作者信息

Sy M S, Dietz M H, Germain R N, Benacerraf B, Greene M I

出版信息

J Exp Med. 1980 May 1;151(5):1183-95. doi: 10.1084/jem.151.5.1183.

Abstract

Administration of azobenzenearsonate (ABA)-coupled syngeneic spleen cells intravenously to A/J mice leads to the generation of suppressor T cells (Ts1) which exhibit specific binding to ABA-bovine serum albumin (BSA)-coated dishes. These Ts1 share idiotypic determinants with the major cross-reactive idiotype (CRI) of the anti-ABA antibodies of A/J mice, and also produce a soluble suppressor factor (TsF) bearing CRI and I-J subregion-coded determinants. Injection of this TsF into naive A/J mice elicits a second set of specific suppressor cells (Ts2) which are not lysed by anti-CRI antibody plus C, and which do not bind to ABA-BSA-coated dishes. However, in contrast with Ts1, these Ts2 do bind to plates bearing CRI+ anti-ABA immunoglobulin. Thus, Ts2 exhibit anti-idiotypic specificity. These data indicate that antigen elicits the production of a soluble T cell product bearing both variable portion of the Ig heavy chain (VH) and I-J subregion-coded determinants which serves to communicate between T cell subsets to establish an idiotype-anti-idiotype regulatory pathway.

摘要

给A/J小鼠静脉注射偶氮苯胂酸盐(ABA)偶联的同基因脾细胞会导致抑制性T细胞(Ts1)的产生,这些细胞表现出与ABA - 牛血清白蛋白(BSA)包被培养皿的特异性结合。这些Ts1与A/J小鼠抗ABA抗体的主要交叉反应独特型(CRI)共享独特型决定簇,并且还产生带有CRI和I-J亚区编码决定簇的可溶性抑制因子(TsF)。将这种TsF注射到未接触过抗原的A/J小鼠中会引发第二组特异性抑制细胞(Ts2),它们不会被抗CRI抗体加补体(C)裂解,并且不与ABA - BSA包被的培养皿结合。然而,与Ts1不同,这些Ts(此处原文有误,应为Ts2)确实会与带有CRI +抗ABA免疫球蛋白的平板结合。因此,Ts2表现出抗独特型特异性。这些数据表明,抗原引发了一种可溶性T细胞产物的产生,该产物同时带有Ig重链可变区(VH)和I-J亚区编码的决定簇,其作用是在T细胞亚群之间进行通信,以建立独特型-抗独特型调节途径。

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