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先天免疫细胞上 Fc 受体表达的降低与慢性 HIV-1 感染个体中抗体介导的细胞吞噬活性受损有关。

Decreased Fc receptor expression on innate immune cells is associated with impaired antibody-mediated cellular phagocytic activity in chronically HIV-1 infected individuals.

机构信息

Ragon Institute of Massachusetts General Hospital, Harvard University and Massachusetts Institute of Technology (formerly known as Partners AIDS Research Center of Massachusetts General Hospital), Boston, MA, USA.

出版信息

Virology. 2011 Jul 5;415(2):160-7. doi: 10.1016/j.virol.2011.03.012. Epub 2011 May 12.

Abstract

In addition to neutralization, antibodies mediate other antiviral activities including antibody-dependent cellular phagocytosis (ADCP), antibody-dependent cellular cytotoxicity (ADCC), as well as complement deposition. While it is established that progressive HIV infection is associated with reduced ADCC and ADCP, the underlying mechanism for this loss of function is unknown. Here we report considerable changes in FcR expression over the course of HIV infection on both mDCs and monocytes, including elevated FcγRI expression in acute HIV infection and reduced expression of FcγRII and FcγRIIIa in chronic HIV infection. Furthermore, selective blockade of FcγRII alone was associated with a loss in ADCP activity, suggesting that FcγRII plays a central role in modulating ADCP. Overall, HIV infection is associated with a number of changes in FcR expression on phagocytic cells that are associated with changes in their ability to respond to antibody-opsonized targets, potentially contributing to a failure in viral clearance in progressive HIV-1 infection.

摘要

除了中和作用,抗体还介导其他抗病毒活性,包括抗体依赖的细胞吞噬作用(ADCP)、抗体依赖的细胞细胞毒性(ADCC)以及补体沉积。虽然已经证实,HIV 感染的进展与 ADCC 和 ADCP 的降低有关,但这种功能丧失的潜在机制尚不清楚。在这里,我们报告了在 HIV 感染过程中,mDC 和单核细胞上 FcR 表达的显著变化,包括急性 HIV 感染中 FcγRI 的表达升高和慢性 HIV 感染中 FcγRII 和 FcγRIIIa 的表达降低。此外,仅选择性阻断 FcγRII 就与 ADCP 活性的丧失有关,表明 FcγRII 在调节 ADCP 中发挥核心作用。总的来说,HIV 感染与吞噬细胞上 FcR 表达的许多变化有关,这些变化与它们对抗体调理靶标的反应能力的变化有关,可能导致 HIV-1 感染进展中病毒清除的失败。

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