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Reduced lysis by CD8+ cytotoxic T cells in mixed lymphocyte reactions induced via CD4+ T cells exposed to chemically modified antigen presenting cells.

机译:在暴露于化学修饰的抗原呈递细胞的CD4 + T细胞诱导的混合淋巴细胞反应中CD8 +细胞毒性T细胞的裂解降低。

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摘要

The resistance by T lymphocytes to activation by antigen (anergy) is well documented for CD4+ T-helper (Th) cells, although less is known about CD8+ cytotoxic T lymphocytes (CTL). One widely used method of inducing anergy of CD4+Th is presentation of antigen by ECDI (1-ethyl-3-(3-dimethylamino-propyl)carbodiimide)-fixed antigen-presenting cells (APCs). We report here that in murine mixed lymphocyte reactions (MLRs), a marked reduction in detected cytotoxicity (which is mediated predominantly by CD8+ CTL) occurs on day 7 if the bulk cultures are restimulated 2 days previously with ECDI-fixed allogeneic splenocytes. No differences were seen between untreated cultures on days 5 and 7, or on day 7 of cultures to which were added unfixed allogeneic splenocytes, fixed or unfixed syngeneic splenocytes, or 'third-party' allogeneic splenocytes, 2 days previously. The effect is not mediated directly on CD8+ cells, since MLRs depleted of CD4+ cells immediately prior to exposure to fixed allogeneic splenocytes fail to show reduced lysis. On the other hand, reduced lysis did occur if CD4+ cells, purified from the MLRs on day 4, were exposed to ECDI-fixed allogeneic splenocytes and then returned to MLRs previously depleted of CD4+ cells. Moreover the effect is overcome using exogenous interleukin-2 (IL-2). We propose that CD4+ cells, restimulated by a regimen shown previously to induce their anergy, can cause a reduction in CD(8+)-mediated cytotoxicity in MLRs.
机译:尽管对CD8 +细胞毒性T淋巴细胞(CTL)知之甚少,但CD4 + T辅助(Th)细胞对T淋巴细胞对抗原激活的抗性(无能)已有充分的文献记载。一种广泛使用的诱导CD4 + Th无能的方法是通过ECDI(1-乙基-3-(3-二甲基氨基丙基)碳二亚胺)固定的抗原呈递细胞(APC)呈递抗原。我们在这里报告说,如果将大批培养物在2天前用ECDI固定的同种异体脾细胞重新刺激,则在鼠类混合淋巴细胞反应(MLR)中,检测到的细胞毒性显着降低(主要由CD8 + CTL介导)。未处理的培养物在第5天和第7天,或在培养的第7天,在2天前添加未固定的同种异体脾细胞,固定或未固定的同基因脾细胞或“第三方”同种异体脾细胞,未见差异。该作用未直接介导于CD8 +细胞,因为紧接暴露于固定的同种异体脾细胞之前耗尽了CD4 +细胞的MLR未能显示出减少的裂解作用。另一方面,如果将在第4天从MLR中纯化的CD4 +细胞暴露于ECDI固定的同种异体脾细胞,然后返回到先前已耗尽CD4 +细胞的MLR中,则裂解的确发生了。此外,使用外源白介素-2(IL-2)可以克服这种作用。我们建议,CD4 +细胞,由先前显示的诱导其无反应性的疗法再刺激,可导致MLRs中CD(8+)介导的细胞毒性降低。

著录项

  • 期刊名称 Immunology
  • 作者

    L Corlett; D H Davies;

  • 作者单位
  • 年(卷),期 1995(84),3
  • 年度 1995
  • 页码 488–494
  • 总页数 7
  • 原文格式 PDF
  • 正文语种
  • 中图分类 免疫学;
  • 关键词

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