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活化的刺激不应性CD4 + T细胞对T细胞反应的抗原非特异性抑制。

Antigen nonspecific suppression of T cell responses by activated stimulation-refractory CD4+ T cells.

作者信息

Duthoit Christine T, Nguyen Phuong, Geiger Terrence L

机构信息

Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

出版信息

J Immunol. 2004 Feb 15;172(4):2238-46. doi: 10.4049/jimmunol.172.4.2238.

DOI:10.4049/jimmunol.172.4.2238
PMID:14764692
Abstract

Several classes of anergic T cells are capable of suppressing naive T cell proliferation and thereby limiting immune responses. Activated T cells, although not anergic, are transiently refractory to restimulation with Ag. We examine in this study whether activated refractory murine T cells can also suppress naive T cell responses. We find that they can, and that they exhibit many of the suppressive properties of anergic T cells. The activated cells strongly diminish Ag-mediated T cell proliferation, an activity that correlates with their refractory period. Suppression is independent of APC numbers and requires cell contact or proximity. Naive T cells stimulated in the presence of activated refractory cells up-regulate CD25 and CD69, but fail to produce IL-2. The addition of IL-2 to culture medium, however, does not prevent the suppression, which is therefore not solely due to the absence of this growth factor. Persistence of the suppressor cells is also not essential. T cells stimulated in their presence and then isolated from them and cultured do not divide. The suppressive cells, however, do not confer a refractory or anergic state on the target T lymphocytes, which can fully respond to antigenic stimulation if removed from the suppressors. Our results therefore provide evidence that activated T cells act as transient suppressor cells, severely constraining bystander T cell stimulation and thereby restricting their response. These results have potentially broad implications for the development and regulation of immune responses.

摘要

几类无反应性T细胞能够抑制初始T细胞增殖,从而限制免疫反应。活化的T细胞虽然并非无反应性,但对再次用抗原刺激具有短暂的不应性。在本研究中,我们检测活化的不应性小鼠T细胞是否也能抑制初始T细胞反应。我们发现它们能够抑制,并且表现出许多无反应性T细胞的抑制特性。活化细胞强烈减少抗原介导的T细胞增殖,这一活性与其不应期相关。抑制作用不依赖于抗原呈递细胞数量,且需要细胞接触或细胞靠近。在活化的不应性细胞存在的情况下受到刺激的初始T细胞上调CD25和CD69,但不产生白细胞介素-2。然而,向培养基中添加白细胞介素-2并不能阻止抑制作用,因此抑制作用并非仅仅由于缺乏这种生长因子。抑制细胞的持续存在也不是必需的。在抑制细胞存在的情况下受到刺激,然后从抑制细胞中分离并培养的T细胞不分裂。然而,抑制细胞并未赋予靶T淋巴细胞不应性或无反应性状态,若将靶T淋巴细胞从抑制细胞中移除,它们能够对抗原刺激作出充分反应。因此,我们的结果提供了证据表明活化的T细胞作为短暂的抑制细胞,严重限制旁观者T细胞刺激,从而限制其反应。这些结果对免疫反应的发生发展和调节可能具有广泛的意义。

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