Low levels of SIV infection in sooty mangabey central-memory CD4+ T-cells is associated with limited CCR5 expression

Naturally SIV-infected sooty mangabeys (SMs) do not progress to AIDS despite high-level virus replication. We previously showed that the fraction of CD4+CCR5+ T-cells is lower in SMs compared to humans and macaques. Here we found that, after in vitro stimulation, SM CD4+ T-cells fail to up-regulate...

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Bibliographic Details
Main Authors: Paiardini, Mirko, Cervasi, Barbara, Reyes-Aviles, Elane, Micci, Luca, Ortiz, Alexandra M., Chahroudi, Ann, Vinton, Carol, Gordon, Shari N., Bosinger, Steven E., Francella, Nicholas, Hallberg, Paul L., Schlub, Timothy, Chan, Ming Liang, Riddick, Nadeene E., Collman, Ronald G., Apetrei, Cristian, Pandrea, Ivona, Else, James, Munch, Jan, Kirchhoff, Frank, Davenport, Miles P., Brenchley, Jason M., Silvestri, Guido
Format: Online
Language:English
Published: 2011
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253129/
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Summary:Naturally SIV-infected sooty mangabeys (SMs) do not progress to AIDS despite high-level virus replication. We previously showed that the fraction of CD4+CCR5+ T-cells is lower in SMs compared to humans and macaques. Here we found that, after in vitro stimulation, SM CD4+ T-cells fail to up-regulate CCR5, and that this phenomenon is more pronounced in CD4+ central-memory T-cells (TCM). CD4+ T-cell activation was similarly uncoupled from CCR5 expression in SMs in vivo during (i) acute SIV infection and (ii) following antibody-mediated CD4+ T-cell depletion. Remarkably, CD4+ TCM of SMs that express low levels of CCR5 demonstrated reduced susceptibility to SIV infection both in vivo and in vitro when compared to CD4+ TCM of RMs. These data suggest that low CCR5 expression on SM CD4+ T-cells favors the preservation of CD4+ T-cell homeostasis and promotes an AIDS-free status by protecting CD4+ TCM from direct virus infection.