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由一个Db特异性T辅助细胞克隆诱导对同种异体抗原的CTL反应。

Induction of CTL responses to alloantigens by a Db-specific T helper clone.

作者信息

Kwong P C, Kilburn D G, Teh H S

出版信息

J Immunol. 1984 Aug;133(2):653-9.

PMID:6203972
Abstract

A T cell helper clone was derived 2 yr ago from a mixed lymphocyte culture. This clone, referred to as clone 9, was propagated in interleukin 2 (IL 2)-containing medium in the presence of irradiated stimulator and irradiated syngeneic spleen cells. Clone 9 was of H-2d origin and was found to be Thy-1+ and Lyt-1-2-. Clone 9, as well as supernatant factor(s) derived from it, were able to enhance the primary cytotoxic responses of Db responder cells to alloantigens. Furthermore, clone 9 cells or its factor(s) were only active when added during the first 24 hr of a 5-day culture period. When a low stimulator cell dose (10(4) cells per 0.2 ml culture) was used, it was possible to demonstrate that clone 9 also required a source of irradiated allogeneic splenic accessory cells to exert its helper action. Under these conditions, clone 9 or its factor(s) could also synergize with IL 2-containing medium in mounting cytotoxic responses to alloantigens. Synergy between IL 2-containing medium and clone 9 or its factor(s) was observed only when Db responder cells were used. The helper activity in clone 9 supernatant was also specifically absorbed out by Con A-stimulated Db spleen cell blasts. Preincubation with clone 9 supernatant for 1 hr at room temperature also led to enhanced cytotoxic responses of Db responder cells to alloantigens. Clone 9 supernatant was also found to be devoid of detectable IL 2 activity. Thus, clone 9 or its helper factor(s) appear to exert its helper activity by an early interaction with Db cytotoxic T lymphocyte precursors (CTL-P).

摘要

一个T细胞辅助性克隆于2年前从混合淋巴细胞培养物中获得。这个克隆,称为克隆9,在含白细胞介素2(IL-2)的培养基中,于经照射的刺激细胞和经照射的同基因脾细胞存在的情况下进行增殖。克隆9起源于H-2d,被发现为Thy-1+和Lyt-1-2-。克隆9以及从中衍生的上清因子能够增强Db反应细胞对同种异体抗原的初次细胞毒性反应。此外,克隆9细胞或其因子仅在5天培养期的头24小时内添加时才具有活性。当使用低剂量的刺激细胞(每0.2 ml培养物10⁴个细胞)时,有可能证明克隆9还需要经照射的同种异体脾辅助细胞来源才能发挥其辅助作用。在这些条件下,克隆9或其因子也能与含IL-2的培养基协同作用,引发对同种异体抗原的细胞毒性反应。仅当使用Db反应细胞时,才观察到含IL-2的培养基与克隆9或其因子之间的协同作用。克隆9上清液中的辅助活性也被刀豆蛋白A刺激的Db脾细胞母细胞特异性吸收。在室温下用克隆9上清液预孵育1小时也会导致Db反应细胞对同种异体抗原的细胞毒性反应增强。还发现克隆9上清液缺乏可检测到的IL-2活性。因此,克隆9或其辅助因子似乎通过与Db细胞毒性T淋巴细胞前体(CTL-P)的早期相互作用发挥其辅助活性。

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