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在次级淋巴组织中组成性表达的趋化因子增强HIV-1复制。

Enhanced HIV-1 replication by chemokines constitutively expressed in secondary lymphoid tissues.

作者信息

Nagira M, Sato A, Miki S, Imai T, Yoshie O

机构信息

Shionogi Institute for Medical Science, Osaka, 566-0022, Japan.

出版信息

Virology. 1999 Nov 25;264(2):422-6. doi: 10.1006/viro.1999.0011.

Abstract

Persistent infection of human immunodeficiency virus (HIV) takes place in the secondary lymphoid tissues even during clinically latent stages. The CC chemokines secondary lymphoid tissue chemokine (SLC) and EBI1-ligand chemokine (ELC) are constitutively expressed in the secondary lymphoid tissues. They share CCR7 expressed on lymphocytes and mature dendritic cells and play key roles in the trafficking of these types of cells into the secondary lymphoid tissues. Here we report that growth of both X4 and R5 strains of HIV-1 in activated peripheral blood T cells was enhanced by SLC. The enhancing effect of SLC was abrogated by pretreatment of cells with pertussis toxin, indicating the involvement of signaling via a receptor coupled with a Galphai class of G-protein. Furthermore, SLC was found to enhance the promoter activity of HIV-1 LTR. These results suggest that signaling via CCR7 has a strong positive effect on HIV growth. Thus, SLC and ELC may contribute to persistent infection of HIV in the secondary lymphoid tissues by promoting viral replication in activated T cells.

摘要

即使在临床潜伏期,人类免疫缺陷病毒(HIV)也会在次级淋巴组织中持续感染。CC趋化因子次级淋巴组织趋化因子(SLC)和EBI1配体趋化因子(ELC)在次级淋巴组织中组成性表达。它们共享淋巴细胞和成熟树突状细胞上表达的CCR7,并在将这些类型的细胞运输到次级淋巴组织中发挥关键作用。在此我们报告,SLC增强了HIV-1的X4和R5毒株在活化外周血T细胞中的生长。用百日咳毒素预处理细胞可消除SLC的增强作用,表明信号传导涉及通过与Galphai类G蛋白偶联的受体。此外,发现SLC可增强HIV-1 LTR的启动子活性。这些结果表明,通过CCR7的信号传导对HIV生长具有强烈的正向作用。因此,SLC和ELC可能通过促进活化T细胞中的病毒复制,导致HIV在次级淋巴组织中的持续感染。

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