Walker-Sperling Victoria E, Merlo Christian A, Buckheit Robert W, Lambert Allison, Tarwater Patrick, Kirk Greg D, Drummond M Bradley, Blankson Joel N
1 Department of Medicine, Johns Hopkins University School of Medicine , Baltimore, Maryland.
2 Division of Biostatistics and Epidemiology, Paul L. Foster School of Medicine , El Paso, Texas.
AIDS Res Hum Retroviruses. 2016 Oct/Nov;32(10-11):1097-1099. doi: 10.1089/AID.2016.0082. Epub 2016 Aug 2.
Macrophages are targets of HIV-1 infection, and control of viral replication within these cells may be an important component of a T-cell-based vaccine. Although several studies have analyzed the ability of CD8 T cells to inhibit viral replication in monocyte-derived macrophages, the effect of T cells on HIV-1-infected tissue macrophages is less clear. We demonstrate here that both CD4 and CD8 T-cell effectors from HIV controllers are capable of suppressing viral replication in bronchoalveolar lavage-derived alveolar macrophages. These findings have implications for HIV-1 vaccine and eradication strategies.
巨噬细胞是HIV-1感染的靶细胞,控制这些细胞内的病毒复制可能是以T细胞为基础的疫苗的一个重要组成部分。尽管有几项研究分析了CD8 T细胞抑制单核细胞衍生巨噬细胞中病毒复制的能力,但T细胞对HIV-1感染的组织巨噬细胞的影响尚不清楚。我们在此证明,来自HIV控制者的CD4和CD8 T细胞效应器都能够抑制支气管肺泡灌洗来源的肺泡巨噬细胞中的病毒复制。这些发现对HIV-1疫苗和根除策略具有重要意义。