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Ia反应性CD8⁺小鼠T细胞的分化不需要Ia参与。CD4和CD8辅助分子在T细胞分化中的作用探讨。

Differentiation of Ia-reactive CD8+ murine T cells does not require Ia engagement. Implications for the role of CD4 and CD8 accessory molecules in T cell differentiation.

作者信息

Mizuochi T, Tentori L, Sharrow S O, Kruisbeek A M, Singer A

机构信息

Immunology Branch, National Cancer Institute, Bethesda, Maryland 20892.

出版信息

J Exp Med. 1988 Jul 1;168(1):437-42. doi: 10.1084/jem.168.1.437.

Abstract

The present study was undertaken to assess the Ia differentiation requirements of CD8+ class II-allospecific CTL, whose CD8+ phenotype is apparently "discordant" with their MHC class II reactivity. To do so, we compared the effect of in vivo anti-Ia blockade on the differentiation of Ia-reactive CD8+ CTL with its effect on the differentiation of CD4+ T cells. We found that anti-Ia blockade did not detectably interfere with the differentiation of CD8+ Ia-reactive CTL, even though it arrested the differentiation of CD4+ T cells. Thus, the differentiation of CD4+ T cells is strictly dependent upon Ia engagement, whereas the differentiation of CD8+ T cells, even those with reactivity against MHC class II alloantigens, does not require Ia engagement. These results support the concept that Ia-reactive CD8+ T cells are conventional CD8+ CTL, probably selected by self-class I MHC molecules during differentiation, whose receptors fortuitously crossreact on MHC class II alloantigens. Taken together, the present data indicate an intimate relationship between CD4/CD8 expression with MHC class specificity during T cell differentiation and selection. We suggest that an active triggering role for CD4 and CD8 accessory molecules in T cell differentiation is best able to explain these observations.

摘要

本研究旨在评估CD8⁺ Ⅱ类同种异体特异性CTL的Ia分化需求,其CD8⁺ 表型显然与其MHC Ⅱ类反应性“不一致”。为此,我们比较了体内抗Ia阻断对Ia反应性CD8⁺ CTL分化的影响及其对CD4⁺ T细胞分化的影响。我们发现,抗Ia阻断并未明显干扰CD8⁺ Ia反应性CTL的分化,尽管它阻止了CD4⁺ T细胞的分化。因此,CD4⁺ T细胞的分化严格依赖于Ia的参与,而CD8⁺ T细胞的分化,即使是那些对MHC Ⅱ类同种异体抗原具有反应性的细胞,也不需要Ia的参与。这些结果支持了这样一种概念,即Ia反应性CD8⁺ T细胞是传统的CD8⁺ CTL,可能在分化过程中由自身I类MHC分子选择,其受体偶然地与MHC Ⅱ类同种异体抗原发生交叉反应。综上所述,目前的数据表明在T细胞分化和选择过程中,CD4/CD8表达与MHC类特异性之间存在密切关系。我们认为,CD4和CD8辅助分子在T细胞分化中起积极的触发作用最能解释这些观察结果。

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