Echebli Nadia, Tchitchek Nicolas, Dupuy Stéphanie, Bruel Timothée, Peireira Bittencourt Passaes Caroline, Bosquet Nathalie, Le Grand Roger, Bourgeois Christine, Favier Benoit, Cheynier Rémi, Lambotte Olivier, Vaslin Bruno
CEA, Université Paris Sud, INSERM U1184, Immunology of Viral Infections and Autoimmune Diseases (IMVA), IDMIT Department / IBFJ, Fontenay-aux-Roses, France.
Cytokines and Viral Infections, Immunology Infection and Inflammation Department, Institut Cochin, INSERM U1016, Paris, France.
PLoS One. 2018 Jan 11;13(1):e0190334. doi: 10.1371/journal.pone.0190334. eCollection 2018.
Interferons (IFNs) play a major role in controlling viral infections including HIV/SIV infections. Persistent up-regulation of interferon stimulated genes (ISGs) is associated with chronic immune activation and progression in SIV/HIV infections, but the respective contribution of different IFNs is unclear. We analyzed the expression of IFN genes and ISGs in tissues of SIV infected macaques to understand the respective roles of type I and type II IFNs. Both IFN types were induced in lymph nodes during early stage of primary infection and to some extent in rectal biopsies but not in PBMCs. Induction of Type II IFN expression persisted during the chronic phase, in contrast to undetectable induction of type I IFN expression. Global gene expression analysis with a major focus on ISGs revealed that at both acute and chronic infection phases most differentially expressed ISGs were inducible by both type I and type II IFNs and displayed the highest increases, indicating strong convergence and synergy between type I and type II IFNs. The analysis of functional signatures of ISG expression revealed temporal changes in IFN expression patterns identifying phase-specific ISGs. These results suggest that IFN-γ strongly contribute to shape ISG upregulation in addition to type I IFN.
干扰素(IFNs)在控制包括HIV/SIV感染在内的病毒感染中发挥着重要作用。干扰素刺激基因(ISGs)的持续上调与SIV/HIV感染中的慢性免疫激活和疾病进展相关,但不同干扰素各自的作用尚不清楚。我们分析了SIV感染猕猴组织中IFN基因和ISGs的表达,以了解I型和II型干扰素各自的作用。在初次感染的早期阶段,两种类型的干扰素在淋巴结中均被诱导表达,在直肠活检组织中也有一定程度的诱导,但在PBMCs中未被诱导。与I型干扰素无法检测到的诱导情况相反,II型干扰素的表达在慢性期持续存在。主要聚焦于ISGs的全基因组表达分析表明,在急性和慢性感染阶段,大多数差异表达的ISGs均可被I型和II型干扰素诱导,且上调幅度最大,这表明I型和II型干扰素之间存在强烈的趋同和协同作用。对ISG表达功能特征的分析揭示了IFN表达模式的时间变化,确定了阶段特异性的ISGs。这些结果表明,除了I型干扰素外,IFN-γ在塑造ISG上调方面也发挥着重要作用。