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细胞因子调节人类成熟树突状细胞上HIV共受体CXCR4的表达和功能。

Cytokines regulate expression and function of the HIV coreceptor CXCR4 on human mature dendritic cells.

作者信息

Zoeteweij J P, Golding H, Mostowski H, Blauvelt A

机构信息

Dermatology Branch, National Cancer Institute, Bethesda, MD 20892, USA.

出版信息

J Immunol. 1998 Oct 1;161(7):3219-23.

PMID:9759835
Abstract

HIV-infected dendritic cells (DC) efficiently transmit infection to CD4+ T cells during the process of T cell activation. To further understand interactions between DC and HIV, cytokine regulation of HIV coreceptors on cultured Langerhans cells (cLC, as prototypes of mature DC) was studied. Expression of cell surface CXCR4 on cLC was up-regulated by IL-4 and TGF-beta1 and inhibited by IFN-alpha, IFN-beta, and IFN-gamma, whereas cytokines did not appreciably regulate CCR5. Changes in cell surface CXCR4 expression on cLC correlated with T cell-tropic (X4)-HIV envelope-mediated syncytium formation and X4-HIV infection levels. A relative increase in the ratio of type 2/type 1 cytokine production, which can occur in HIV disease, may up-regulate CXCR4 expression on mature DC and promote infection by X4 viruses. Importantly, these findings suggest that cytokine dysregulation may be linked to the emergence of X4-HIV strains as HIV-infected individuals progress to AIDS.

摘要

HIV感染的树突状细胞(DC)在T细胞激活过程中能有效地将感染传递给CD4+ T细胞。为了进一步了解DC与HIV之间的相互作用,研究了细胞因子对培养的朗格汉斯细胞(cLC,作为成熟DC的原型)上HIV共受体的调节作用。cLC表面CXCR4的表达受IL-4和TGF-β1上调,而受IFN-α、IFN-β和IFN-γ抑制,而细胞因子对CCR5没有明显调节作用。cLC表面CXCR4表达的变化与T细胞嗜性(X4)-HIV包膜介导的合胞体形成及X4-HIV感染水平相关。在HIV疾病中可能出现的2型/1型细胞因子产生比例的相对增加,可能会上调成熟DC上CXCR4的表达并促进X4病毒的感染。重要的是,这些发现表明,随着HIV感染个体进展为艾滋病,细胞因子失调可能与X4-HIV毒株的出现有关。

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