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CD80在CD4+细胞毒性T细胞生成中的作用。

Involvement of CD80 in the generation of CD4+ cytotoxic T cells.

作者信息

Mauri D, Pichler W J

机构信息

Institute of Immunology and Allergology, Bern, Switzerland.

出版信息

Immunol Res. 1996;15(2):126-40. doi: 10.1007/BF02918502.

Abstract

CD4+ T cells can exert different effector functions, which are partly distinguishable by the secretion of different cytokines, namely by either IFN-gamma, IL-2 and lymphotoxins for Th1-like or IL-4, IL-5, IL-10 and IL-13 for Th2-like T cells. Th1-like T cells can exert cytotoxic functions, too. The cytokinetic phenotype of an activated T cell clone (TCC) is mainly influenced by the cytokinetic pattern of the microenvironment where it was activated. However, the interaction between certain adhesion molecules (i.e. CD28-CD80 and CD28-CD86) may also have an influence on the functionality of the reactive T cell. On the contrary, the requirements for the induction of CD4+ cytotoxic T cells (CD4+ CTLs) are not well understood. We have focused this review on studies investigating the development of CD4+ T cells with cytotoxic effector functions. In particular, we discuss here whether the type of antigen-presenting cells (APCs) and the distinct expression of important adhesion molecules like CD80 and CD86 may influence the generation of CD4+ CTLs. Among a large panel of APCs only dendritic cells and TCCs are able to induce cytotoxicity. The level of CD80, but not of CD86, present on the APCs appears to be crucial for the induction of CD4+ CTLs.

摘要

CD4+ T细胞可发挥不同的效应功能,部分可通过不同细胞因子的分泌来区分,即Th1样细胞分泌干扰素-γ、白细胞介素-2和淋巴毒素,而Th2样T细胞分泌白细胞介素-4、白细胞介素-5、白细胞介素-10和白细胞介素-13。Th1样T细胞也可发挥细胞毒性功能。活化的T细胞克隆(TCC)的细胞因子表型主要受其活化时微环境的细胞因子模式影响。然而,某些黏附分子(即CD28-CD80和CD28-CD86)之间的相互作用也可能影响反应性T细胞的功能。相反,诱导CD4+细胞毒性T细胞(CD4+ CTL)的条件尚不清楚。本综述重点关注了研究具有细胞毒性效应功能的CD4+ T细胞发育的研究。特别是,我们在此讨论抗原呈递细胞(APC)的类型以及重要黏附分子如CD80和CD86的不同表达是否可能影响CD4+ CTL的产生。在众多APC中,只有树突状细胞和TCC能够诱导细胞毒性。APC上CD80的水平而非CD86的水平似乎对诱导CD4+ CTL至关重要。

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