首页> 外文OA文献 >Generation and characterization of a continuous line of CD8+ suppressively regulatory T lymphocytes which down-regulates experimental autoimmune orchitis (EAO) in mice.
【2h】

Generation and characterization of a continuous line of CD8+ suppressively regulatory T lymphocytes which down-regulates experimental autoimmune orchitis (EAO) in mice.

机译:连续下调CD8 +抑制性T淋巴细胞的产生和表征,该T细胞下调小鼠的实验性自身免疫性睾丸炎(EAO)。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We have previously shown that two injections with viable syngeneic testicular germ cells (TC) alone developed experimental autoimmune orchitis (EAO) in C3H/He mice, and that the induction of antigen-specific tolerance in this EAO model is associated with the generation of antigen-specific suppressively regulatory T (Ts) cells. For the elucidation of the nature of these Ts cells, a murine Ts cell line (designated Ts-A) was established. This line was generated from the spleen cells of C3H/He mice which had received three i.v. injections of a soluble (deaggregated) form of murine testicular antigen (mTA), followed by the repeated selection of these spleen lymphocytes in vitro by stimulation with mTA. Adoptive transfer of Ts-A cells into naive syngeneic mice immediately before the first TC injection was found to downgrade EAO in actively immunized recipients. The transferred Ts-A cells significantly inhibited the cellular immune response to TC in the recipients in an antigen-specific manner, but these cells had no inhibitory effect on the humoral immune response to TC. This line could also inhibit in vitro syngeneic TC-driven proliferation of orchitogenic lymphocytes. Surface phenotype of this line was CD8+, CD4-, Thy-1.2+, CD3+, and TCR alpha beta+. These findings may suggest an in vivo role for suppressively regulatory lymphocytes, capable of inhibiting helper T cells, in the regulation of EAO.
机译:我们以前已经表明,两次注射有活力的同基因睾丸生殖细胞(TC)单独在C3H / He小鼠中发展了实验性自身免疫性睾丸炎(EAO),并且这种EAO模型中抗原特异性耐受的诱导与抗原的产生有关特异性抑制性调节性T(Ts)细胞。为了阐明这些Ts细胞的性质,建立了鼠Ts细胞系(命名为Ts-A)。该系由接受3次静脉内注射的C3H / He小鼠的脾细胞产生。注射可溶性(分解)形式的鼠睾丸抗原(mTA),然后在体外通过mTA刺激重复选择这些脾淋巴细胞。在第一次进行TC注射之前,立即将Ts-A细胞过继转移到幼稚的同系小鼠中,从而降低了主动免疫受体的EAO。转移的Ts-A细胞以抗原特异性方式显着抑制受体中对TC的细胞免疫应答,但是这些细胞对体液对TC的免疫应答没有抑制作用。该品系还可以抑制体外同基因TC驱动的促睾淋巴细胞的增殖。该细胞系的表面表型为CD8 +,CD4-,Thy-1.2 +,CD3 +和TCR alpha beta +。这些发现可能暗示在EAO的调节中,能够抑制辅助性T细胞的抑制性调节淋巴细胞的体内作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号