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人巨细胞病毒抑制细胞因子诱导的巨噬细胞分化。

Human cytomegalovirus inhibits cytokine-induced macrophage differentiation.

作者信息

Gredmark Sara, Tilburgs Tamara, Söderberg-Nauclér Cecilia

机构信息

Karolinska Systems Biomedicine Center, Department of Medicine, Center for Molecular Medicine, Karolinska Institute, S-171 76 Stockholm, Sweden.

出版信息

J Virol. 2004 Oct;78(19):10378-89. doi: 10.1128/JVI.78.19.10378-10389.2004.

Abstract

Human cytomegalovirus (HCMV) infection in immunocompromised patients is associated with impaired immunological function. Blood monocytes, which differentiate into macrophage effector cells, are of central importance for immune reactivity. Here, we demonstrate that HCMV transiently blocks cytokine-induced differentiation of monocytes into functionally active phagocytic macrophages. In HCMV-treated cultures, the cells had classical macrophage markers but lacked the classical morphological appearance of macrophages and had impairments in migration and phagocytosis. Even at very low multiplicities of infection, macrophage differentiation was almost completely inhibited. The inhibition appeared to be mediated by a soluble factor released upon viral treatment of monocytes. Human immunodeficiency virus or measles virus had no such effects. These findings suggest that HCMV impairs immune function by blocking certain aspects of cytokine-induced differentiation of monocytes and demonstrate an efficient pathway for this virus to evade immune recognition that may have clinical implications for the generalized immunosuppression often observed in HCMV-infected patients.

摘要

免疫功能低下患者的人巨细胞病毒(HCMV)感染与免疫功能受损有关。血液单核细胞可分化为巨噬细胞效应细胞,对免疫反应至关重要。在此,我们证明HCMV可短暂阻断细胞因子诱导的单核细胞分化为功能活跃的吞噬性巨噬细胞。在HCMV处理的培养物中,细胞具有经典的巨噬细胞标志物,但缺乏巨噬细胞的经典形态外观,并且在迁移和吞噬方面存在缺陷。即使在非常低的感染复数下,巨噬细胞分化也几乎被完全抑制。这种抑制似乎是由病毒处理单核细胞后释放的一种可溶性因子介导的。人类免疫缺陷病毒或麻疹病毒没有这种作用。这些发现表明,HCMV通过阻断细胞因子诱导的单核细胞分化的某些方面来损害免疫功能,并证明了该病毒逃避免疫识别的有效途径,这可能对HCMV感染患者中经常观察到的全身性免疫抑制具有临床意义。

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