| Literature DB >> 27085913 |
Dan H Barouch1, Khader Ghneim2, William J Bosche3, Yuan Li3, Brian Berkemeier3, Michael Hull3, Sanghamitra Bhattacharyya2, Mark Cameron2, Jinyan Liu4, Kaitlin Smith4, Erica Borducchi4, Crystal Cabral4, Lauren Peter4, Amanda Brinkman4, Mayuri Shetty4, Hualin Li4, Courtney Gittens5, Chantelle Baker5, Wendeline Wagner5, Mark G Lewis5, Arnaud Colantonio6, Hyung-Joo Kang7, Wenjun Li7, Jeffrey D Lifson3, Michael Piatak3, Rafick-Pierre Sekaly2.
Abstract
The earliest events following mucosal HIV-1 infection, prior to measurable viremia, remain poorly understood. Here, by detailed necropsy studies, we show that the virus can rapidly disseminate following mucosal SIV infection of rhesus monkeys and trigger components of the inflammasome, both at the site of inoculation and at early sites of distal virus spread. By 24 hr following inoculation, a proinflammatory signature that lacked antiviral restriction factors was observed in viral RNA-positive tissues. The early innate response included expression of NLRX1, which inhibits antiviral responses, and activation of the TGF-β pathway, which negatively regulates adaptive immune responses. These data suggest a model in which the virus triggers specific host mechanisms that suppress the generation of antiviral innate and adaptive immune responses in the first few days of infection, thus facilitating its own replication. These findings have important implications for the development of vaccines and other strategies to prevent infection.Entities:
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Year: 2016 PMID: 27085913 PMCID: PMC4842119 DOI: 10.1016/j.cell.2016.03.021
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582