首页> 美国卫生研究院文献>Clinical and Experimental Immunology >Antigen-dependent in vitro culture of protective T cells from BCG-primed mice.
【2h】

Antigen-dependent in vitro culture of protective T cells from BCG-primed mice.

机译:来自BCG致敏小鼠的保护性T细胞的抗原依赖性体外培养。

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

Induction of protective immunity against pathogenic mycobacteria depends on vaccination with live organisms such as Bacille Calmette-Guérin (BCG). However, it is not known how many and which antigens are involved in the protective host response. In this study, we developed a system of antigen-dependent in vitro culture which is suitable for the analysis of protective subunits, presented in a soluble form. Spleen cells from Mycobacterium bovis BCG-immune mice, enriched for T cells and depleted of adherent cells on a column of G-10 Sephadex, were cultured for periods varying between 3 and 14 days before transfer and challenge with M. tuberculosis in irradiated hosts. Following 10 days in culture, immune T cells sustained their capacity to transfer protection to tuberculous infection when incubated in the presence of either live BCG or a soluble extract from M. tuberculosis, but lost this ability when cultured in the absence of antigen, or in the presence of the polyclonal mitogen concanavalin A. One immunodominant antigen, represented by the recombinant 38-kD antigen, failed to sustain the adoptive protection, despite pronounced stimulation of lymphoproliferation in culture. Antigenic in vitro stimulation of protective T cells was accompanied by enhanced responsiveness to exogenous IL-2. The experimental system described may be generally suitable to test in vitro the protective potentials of soluble molecular subunits of mycobacteria.
机译:对致病性分枝杆菌的保护性免疫的诱导取决于对活生物体(如巴克·卡莱梅特·盖林(BCG))的接种。然而,尚不知道保护性宿主应答中涉及多少种抗原以及哪些抗原。在这项研究中,我们开发了一种抗原依赖的体外培养系统,适用于分析以可溶性形式存在的保护性亚基。将来自牛分枝杆菌BCG免疫小鼠的脾细胞富集T细胞并去除G-10 Sephadex色谱柱上的贴壁细胞,然后在转移和接受辐照宿主的结核分枝杆菌攻击之前培养3至14天。培养10天后,在活的BCG或结核分枝杆菌的可溶性提取物存在下孵育时,免疫T细胞仍具有将保护转移至结核感染的能力,但在没有抗原或在无抗原的条件下培养时,则失去了这种能力。尽管明显刺激了培养物中的淋巴细胞增殖,但以重组38-kD抗原为代表的一种免疫优势抗原未能维持过继性保护作用。抗原性保护性T细胞的体外刺激伴随着对外源IL-2的增强反应性。所述的实验系统通常可以适合于体外测试分枝杆菌的可溶性分子亚基的保护潜力。

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