R5 HIV-1 envelope attracts dendritic cells to cross the human intestinal epithelium and sample luminal virions via engagement of the CCR5

被引:58
作者
Cavarelli, Mariangela [1 ]
Foglieni, Chiara [1 ]
Rescigno, Maria [2 ]
Scarlatti, Gabriella [1 ]
机构
[1] Ist Sci San Raffaele, DITID, Unit Viral Evolut & Transmiss, I-20132 Milan, Italy
[2] European Inst Oncol, Dept Expt Oncol, Milan, Italy
关键词
dendritic cells; HIV-1; mucosal transmission; HUMAN-IMMUNODEFICIENCY-VIRUS; CD4(+) T-CELLS; INTRAVAGINAL INOCULATION; MICROBIAL TRANSLOCATION; PRODUCTIVE INFECTION; MASSIVE INFECTION; CORECEPTOR USAGE; BARRIER FUNCTION; RHESUS MACAQUES; LONG-TERM;
D O I
10.1002/emmm.201202232
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
The gastrointestinal tract is a principal route of entry and site of persistence of human immunodeficiency virus type 1 (HIV-1). The intestinal mucosa, being rich of cells that are the main target of the virus, represents a primary site of viral replication and CD4+ T-cell depletion. Here, we show both in vitro and ex vivo that HIV-1 of R5 but not X4 phenotype is capable of selectively triggering dendritic cells (DCs) to migrate within 30min between intestinal epithelial cells to sample virions and transfer infection to target cells. The engagement of the chemokine receptor 5 on DCs and the viral envelope, regardless of the genetic subtype, drive DC migration. Viruses penetrating through transient opening of the tight junctions likely create a paracellular gradient to attract DCs. The formation of junctions with epithelial cells may initiate a haptotactic process of DCs and at the same time favour cell-to-cell viral transmission. Our findings indicate that HIV-1 translocation across the intestinal mucosa occurs through the selective engagement of DCs by R5 viruses, and may guide the design of new prevention strategies. See accompanying article http://dx.doi.org/10.1002/emmm.201302763
引用
收藏
页码:776 / 794
页数:19
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