Hertoghs Nina, van der Aar Angelic M G, Setiawan Laurentia C, Kootstra Neeltje A, Gringhuis Sonja I, Geijtenbeek Teunis B H
Department of Experimental Immunology, Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, the Netherlands; and.
Department of Experimental Immunology, Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, the Netherlands; and Laboratory of Viral Immune Pathogenesis, Department of Experimental Immunology, Center for Infection and Immunity Amsterdam, Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, the Netherlands.
J Immunol. 2015 May 1;194(9):4431-7. doi: 10.4049/jimmunol.1403016. Epub 2015 Mar 30.
A hallmark of HIV-1 infection is the lack of sterilizing immunity. Dendritic cells (DCs) are crucial in the induction of immunity, and lack of DC activation might underlie the absence of an effective anti-HIV-1 response. We have investigated how HIV-1 infection affects maturation of DCs. Our data show that even though DCs are productively infected by HIV-1, infection does not induce DC maturation. HIV-1 infection actively suppresses DC maturation, as HIV-1 infection inhibited TLR-induced maturation of DCs and thereby decreased the immune stimulatory capacity of DCs. Interfering with SAMHD1 restriction further increased infection of DCs, but did not lead to DC maturation. Notably, higher infection observed with SAMHD1 depletion correlated with a stronger suppression of maturation. Furthermore, blocking reverse transcription rescued TLR-induced maturation. These data strongly indicate that HIV-1 replication does not trigger immune activation in DCs, but that HIV-1 escapes immune surveillance by actively suppressing DC maturation independent of SAMHD1. Elucidation of the mechanism of suppression can lead to promising targets for therapy or vaccine design.
HIV-1感染的一个标志是缺乏无菌免疫。树突状细胞(DCs)在免疫诱导中至关重要,DC激活的缺乏可能是缺乏有效的抗HIV-1反应的基础。我们研究了HIV-1感染如何影响DCs的成熟。我们的数据表明,尽管DCs被HIV-1有效感染,但感染并未诱导DC成熟。HIV-1感染积极抑制DC成熟,因为HIV-1感染抑制了TLR诱导的DC成熟,从而降低了DC的免疫刺激能力。干扰SAMHD1限制进一步增加了DCs的感染,但并未导致DC成熟。值得注意的是,SAMHD1缺失时观察到的更高感染率与更强的成熟抑制相关。此外,阻断逆转录可挽救TLR诱导的成熟。这些数据强烈表明,HIV-1复制不会触发DCs中的免疫激活,而是HIV-1通过独立于SAMHD1积极抑制DC成熟来逃避免疫监视。阐明抑制机制可为治疗或疫苗设计带来有前景的靶点。