The engagement of activating FcγRs inhibits primate lentivirus replication in human macrophages

被引:30
作者
David, Annie
Saez-Cirion, Asier
Versmisse, Pierre
Malbec, Odile
Iannascoli, Bruno
Herschke, Florence
Lucas, Marianne
Barre-Sinoussi, Francoise
Mouscadet, Jean-Francois
Daeron, Marc
Pancino, Gianfranco
机构
[1] Inst Pasteur, Unite Regulat Infect Retrovirales, F-75726 Paris 15, France
[2] Inst Pasteur, Unite Allergol Mol & Cellulaire, Paris, France
[3] INSERM, Unite 760, Paris, France
[4] Inst Pasteur, Unite Postulante Interact Mol Flavivirus Hotes, Paris, France
[5] Ecole Normale Super, CNRS, Lab Biotechnol & Pharmacol Genet Appl, UMR 8113, Cachan, France
关键词
D O I
10.4049/jimmunol.177.9.6291
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We previously reported that the stimulation of monocyte-derived macrophages (MDM) by plate-bound i.v. Igs inhibits HIV-1 replication. In this study, we show that IgG immune complexes also suppress HIV-1 replication in MDMs and that activating receptors for the Fc portion of IgG-Fc gamma RI, FcyRIIA, and FcyRIII-are responsible for the inhibition. MDM stimulation through Fc gamma Rs induces activation signals and the secretion of HIV-1 modulatory cytokines, such as M-CSF, TNF-alpha, and macrophage-derived chemokine. However, none of these cytokines contribute to HIV-1 suppression. HIV-1 entry and postintegration steps of viral replication are not affected, whereas reduced levels of reverse transcription products and of integrated proviruses, as determined by real-time PCR analysis, account for the suppression of HIV-1 gene expression in Fc gamma R-activated MDMs. We found that Fc gamma R-dependent activation of MDMs also inhibits the replication of HIV-2, SIVmac, and SIVagm, suggesting a common control mechanism for primate immunodeficiency lentiviruses inactivated macrophages.
引用
收藏
页码:6291 / 6300
页数:10
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