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抗原特异性T细胞介导的抑制作用。II. 由I-J编码的L-谷氨酸50-L-酪氨酸50(GT)特异性T细胞抑制因子(GT-T8F)在体外诱导带有不同I-J决定簇的抑制性T细胞(T82)。

Antigen-specific T cell-mediated suppression. II. In vitro induction by I-J-coded L-glutamic acid50-L-tyrosine50 (GT)-specific T cell suppressor factor (GT-T8F) of suppressor T cells (T82) bearing distinct I-J determinants.

作者信息

Germain R N, Theze J, Waltenbaugh C, Dorf M E, Benacerraf B

出版信息

J Immunol. 1978 Aug;121(2):602-7.

PMID:79609
Abstract

The induction of new suppressor T cells (Ts2) by suppressive extracts (TsF) from L-glutamic acid50L-tyrosine50 (GT) nonresponder mice was examined. Incubation of normal spleen cells with allogeneic GT-TsF for 2 days in vitro led to the generation of Ts2 cells able to suppress subsequent responses to the immunogen GT-methylated bovine serum albumin (GT-MBSA) in vivo. This induction occurred efficiently when TsF donor and target cells differed at all of H-2, including the I-J subregion. B10.BR (H-2k) GT-TsF, adsorbed on, then acid eluted from GT-Sepharose and anti-I-Jk [B10.A (3R) anti-B10.A (5R)]-Sepharose in a sequential fashion could induce BALB/c (H-2d) spleen cells to become Ts2 only if nanogram quantities of GT were added to the purified GT-TsF. This indicates a requirement for a molecule or molecular complex possessing both I-J determinants and antigen (GT)-binding specificity, together with GT itself, for Ts2 induction. The induced Ts2 are I-J+, since their function can be eliminated by treatment with anti-I-Jk plus C. These I-J determinants are coded for by the precursor of the Ts2 and do not represent passively adsorbed, I-J coded TsF, since anti-Ijk antiserum [(3R X DBA/2)F1 anti-5R] which cannot recognize the BALB/c (I-Jd) TsF used for induction still eliminates the activity of induced A/J (I-Jk) Ts2. These data provide further evidence for and information about the minimum of two T cells involved in antigen-specific suppressor T cell systems.

摘要

研究了来自L-谷氨酸50L-酪氨酸50(GT)无反应小鼠的抑制性提取物(TsF)对新的抑制性T细胞(Ts2)的诱导作用。将正常脾细胞与同种异体GT-TsF在体外孵育2天,可导致Ts2细胞的产生,这些细胞能够在体内抑制随后对免疫原GT-甲基化牛血清白蛋白(GT-MBSA)的反应。当TsF供体细胞和靶细胞在包括I-J亚区在内的所有H-2位点都存在差异时,这种诱导作用能有效发生。B10.BR(H-2k)GT-TsF依次吸附在GT-琼脂糖上,然后用酸洗脱,再吸附在抗I-Jk [B10.A(3R)抗B10.A(5R)]-琼脂糖上,只有在向纯化的GT-TsF中加入纳克量的GT时,才能诱导BALB/c(H-2d)脾细胞成为Ts2。这表明Ts2诱导需要一种同时具有I-J决定簇和抗原(GT)结合特异性的分子或分子复合物以及GT本身。诱导产生的Ts2是I-J阳性的,因为用抗I-Jk加补体处理可消除其功能。这些I-J决定簇由Ts2的前体细胞编码,并不代表被动吸附的、I-J编码的TsF,因为不能识别用于诱导的BALB/c(I-Jd)TsF的抗Ijk抗血清[(3R×DBA/2)F1抗5R]仍能消除诱导产生的A/J(I-Jk)Ts2的活性。这些数据为抗原特异性抑制性T细胞系统中至少涉及两种T细胞提供了进一步的证据和信息。

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