Blanchet, Fabien, Moris, Arnaud, Nikolic, Damjan S., Lehmann, Martin, Cardinaud, Sylvain, Stalder, Romaine, Garcia, Eduardo, Dinkins, Christina, Leuba, Florence, Wu, Li, Schwartz, Olivier, Deretic, Vojo and Piguet, Vincent 2010. Human immunodeficiency virus-1 inhibition of immunoamphisomes in dendritic cells impairs early innate and adaptive immune responses. Immunity 32 (5) , pp. 654-669. 10.1016/j.immuni.2010.04.011 |
Abstract
Dendritic cells (DCs) in mucosal surfaces are early targets for human immunodeficiency virus-1 (HIV-1). DCs mount rapid and robust immune responses upon pathogen encounter. However, immune response in the early events of HIV-1 transmission appears limited, suggesting that HIV-1 evade early immune control by DCs. We report that HIV-1 induces a rapid shutdown of autophagy and immunoamphisomes in DCs. HIV-1 envelope activated the mammalian target of rapamycin pathway in DCs, leading to autophagy exhaustion. HIV-1-induced inhibition of autophagy in DC increased cell-associated HIV-1 and transfer of HIV-1 infection to CD4+ T cells. HIV-1-mediated downregulation of autophagy in DCs impaired innate and adaptive immune responses. Immunoamphisomes in DCs engulf incoming pathogens and appear to amplify pathogen degradation as well as Toll-like receptor responses and antigen presentation. The findings that HIV-1 downregulates autophagy and impedes immune functions of DCs represent a pathogenesis mechanism that can be pharmacologically countered with therapeutic and prophylactic implications.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Medicine Systems Immunity Research Institute (SIURI) |
Subjects: | Q Science > QR Microbiology > QR180 Immunology |
Uncontrolled Keywords: | Molimmuno; microbio; cellbio |
Publisher: | Elsevier |
ISSN: | 1074-7613 |
Last Modified: | 04 Jun 2017 04:21 |
URI: | https://orca.cardiff.ac.uk/id/eprint/37359 |
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