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诱导CD4+CD25+ T细胞抑制功能的激活要求。

Activation requirements for the induction of CD4+CD25+ T cell suppressor function.

作者信息

Thornton Angela M, Piccirillo Ciriaco A, Shevach Ethan M

机构信息

Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda 20892-1892, USA.

出版信息

Eur J Immunol. 2004 Feb;34(2):366-76. doi: 10.1002/eji.200324455.

Abstract

The in vivo differentiation/survival of CD4(+)CD25(+) T suppressor cells is dependent on IL-2 and CD28-mediated costimulatory signals. To determine the cytokine and costimulatory requirements for CD25(+) T cells in vitro, we established a two-stage culture system where CD25(+) T cells were activated in a primary culture. In the subsequent culture, activated CD4(+)CD25(+) cells were then mixed with responders in order to assess their suppressor function. Pre-culture of CD25(+) T cells with anti-CD3 alone resulted in poor survival and minimal induction of suppressor activity. Pre-culture in the presence of anti-CD3 and IL-2 or IL-4, but not IL-6, IL-7, IL-9, IL-10 or IL-15, resulted in proliferation of the CD25(+) cells and induction of potent suppressor function. Inhibition of the interaction of CD28 or cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) with CD80/CD86 in the pre-culture of CD4(+)CD25(+) cells did not prevent the induction of suppressor function. Furthermore, the inhibition of costimulatory signals did not inhibit the ability of fresh CD25(+) T cells to inhibit CD8(+) responders under conditions where activation of the responders was independent of CD80/CD86. These studies support the view that activation of CD25(+) T cells requires IL-2/IL-4 for their survival/differentiation into effector cells, but is independent of CD28/CTLA-4-mediated costimulation.

摘要

CD4(+)CD25(+) 调节性T细胞在体内的分化/存活依赖于白细胞介素-2(IL-2)和CD28介导的共刺激信号。为了确定体外培养CD25(+) T细胞所需的细胞因子和共刺激条件,我们建立了一个两阶段培养系统,其中CD25(+) T细胞在原代培养中被激活。在随后的培养中,将活化的CD4(+)CD25(+) 细胞与反应细胞混合,以评估它们的抑制功能。单独用抗CD3对CD25(+) T细胞进行预培养,导致细胞存活不佳且抑制活性诱导极少。在抗CD3和IL-2或IL-4存在下进行预培养,但不是IL-6、IL-7、IL-9、IL-10或IL-15,导致CD25(+) 细胞增殖并诱导出强大的抑制功能。在CD4(+)CD25(+) 细胞的预培养中,抑制CD28或细胞毒性T淋巴细胞相关抗原4(CTLA-4)与CD80/CD86的相互作用并不能阻止抑制功能的诱导。此外,在反应细胞的激活不依赖于CD80/CD86的条件下,共刺激信号的抑制并不抑制新鲜CD25(+) T细胞抑制CD8(+) 反应细胞的能力。这些研究支持这样一种观点,即CD25(+) T细胞的激活需要IL-2/IL-4来实现其存活/分化为效应细胞,但独立于CD28/CTLA-4介导的共刺激。

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