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具有CD38(+)CD62L(+)的静息CD4(+) T细胞产生白细胞介素-4,这有助于增强嗜T细胞性1型人类免疫缺陷病毒的复制。

Resting CD4(+) T cells with CD38(+)CD62L(+) produce interleukin-4 which contributes to enhanced replication of T-tropic human immunodeficiency virus type 1.

作者信息

Horikoshi Haruko, Kinomoto Masanobu, Kurosu Takeshi, Komoto Satoshi, Shiraga Miki, Otake Toru, Mukai Tetsu, Ikuta Kazuyoshi

机构信息

Department of Virology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan.

出版信息

Virology. 2002 Feb 1;293(1):94-102. doi: 10.1006/viro.2001.1272.

DOI:10.1006/viro.2001.1272
PMID:11853403
Abstract

A significant increase in the CD38(+) population among T lymphocytes has been observed in human immunodeficiency virus type 1 (HIV-1)-infected carriers. We previously reported a higher replication rate of T-tropic HIV-1 in the CD4(+)CD38(+)CD62L(+) than CD38(-) subset under conditions of mitogen stimulation after infection. Here, we revealed a similarly high susceptibility in the CD38(+) subset on culture with conditioned medium containing Th2 cytokine, interleukin (IL)-4 that was produced endogenously from this subset on stimulation with mitogen or anti-CD3 antibody for 3 days. The contribution of IL-4 to the upregulated production of virus in the CD38(+) subset was confirmed by culture of this subset with recombinant human IL-4. In contrast, the rate of replication in the CD38(-) subset was not augmented in the conditioned medium from either subset or with IL-4. However, there were no differences in the surface expression of IL-4 receptor or HIV-1 receptors CD4 and CXCR4 between the two subsets. Thus, the CD4(+)CD38(+)CD62L(+) subset comprises a specific cell population secreting endogenous Th2 cytokine that contributes to the efficient production of T-tropic HIV-1 through upregulation at a certain stage of the viral life cycle, probably after the adsorption step.

摘要

在人类免疫缺陷病毒1型(HIV-1)感染携带者中,已观察到T淋巴细胞中CD38(+)群体显著增加。我们之前报道,感染后在有丝分裂原刺激条件下,嗜T细胞型HIV-1在CD4(+)CD38(+)CD62L(+)亚群中的复制率高于CD38(-)亚群。在此,我们发现,用含有Th2细胞因子白细胞介素(IL)-4的条件培养基培养时,CD38(+)亚群具有同样高的易感性,IL-4是该亚群在有丝分裂原或抗CD3抗体刺激3天后内源性产生的。用重组人IL-4培养该亚群,证实了IL-4对CD38(+)亚群中病毒产生上调的作用。相比之下,CD38(-)亚群在来自任一亚群的条件培养基中或用IL-4培养时,其复制率均未增加。然而,两个亚群之间IL-4受体或HIV-1受体CD4和CXCR4的表面表达没有差异。因此,CD4(+)CD38(+)CD62L(+)亚群包含一个分泌内源性Th2细胞因子的特定细胞群体,该细胞因子通过在病毒生命周期的某个阶段(可能在吸附步骤之后)上调,有助于嗜T细胞型HIV-1的高效产生。

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引用本文的文献

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