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CD8 T细胞转变为产生TH2细胞因子并辅助B细胞的非细胞溶解性CD8-CD4-细胞。

Switch of CD8 T cells to noncytolytic CD8-CD4- cells that make TH2 cytokines and help B cells.

作者信息

Erard F, Wild M T, Garcia-Sanz J A, Le Gros G

机构信息

Department of Allergy/Immunology, Ciba-Geigy Ltd., Basel, Switzerland.

出版信息

Science. 1993 Jun 18;260(5115):1802-5. doi: 10.1126/science.8511588.

Abstract

CD8+ T cells are a major defense against viral infections and intracellular parasites. Their production of interferon-gamma (IFN-gamma) and their cytolytic activity are key elements in the immune response to these pathogens. Mature mouse CD8+ T cells that were activated in the presence of interleukin-4 (IL-4) developed into a CD8-CD4- population that was not cytolytic and did not produce IFN-gamma. However, these CD8- cells produced large amounts of IL-4, IL-5, and IL-10 and helped activate resting B cells. Thus, CD8 effector functions are potentially diverse and could be exploited by infectious agents that switch off host protective cytolytic responses.

摘要

CD8 + T细胞是抵御病毒感染和细胞内寄生虫的主要防线。它们产生的γ干扰素(IFN - γ)及其细胞溶解活性是针对这些病原体的免疫反应中的关键要素。在白细胞介素-4(IL - 4)存在的情况下被激活的成熟小鼠CD8 + T细胞会发育成一个不具有细胞溶解活性且不产生IFN - γ的CD8 - CD4 - 群体。然而,这些CD8 - 细胞会产生大量的IL - 4、IL - 5和IL - 10,并有助于激活静止的B细胞。因此,CD8效应功能可能具有多样性,并且可能被关闭宿主保护性细胞溶解反应的感染因子所利用。

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