| Literature DB >> 27406996 |
David Shasha1, Dan Karel1, Olivia Angiuli1, Adam Greenblatt1, Musie Ghebremichael1, Xu Yu1, Filippos Porichis2, Bruce D Walker3.
Abstract
Mechanisms modulating HIV-specific CD8+ T cell-mediated viral inhibition are not well defined. To delineate features of effective control, we compared the ability of CD8+ T cells from HIV ECs and CPs to inhibit HIV ex vivo. ECs showed superior inhibition compared to HAART-treated or untreated CPs in a typical VIA in which CD8+ T cells are rested 3 d before use (P = 0.025). In contrast, comparable antiviral activity was observed in freshly thawed cells. Rested CD8+ T cells underwent apoptosis with preferential loss of HIV-specific cells. EC CD8+ T cells showed greater capacity to sustain polyfunctionality ex vivo compared with those of CPs, and incubation of CD8+ T cells with IL-15 augmented inhibition. These results indicate that superior ex vivo inhibition of viral replication by CD8+ T cells from ECs is associated with enhanced retention of functional qualities and that in vitro antiviral function is enhanced by IL-15. © Society for Leukocyte Biology.Entities:
Keywords: HIV control; IL-15; apoptosis; polyfunctionality
Mesh:
Substances:
Year: 2016 PMID: 27406996 PMCID: PMC5109996 DOI: 10.1189/jlb.4A0915-422R
Source DB: PubMed Journal: J Leukoc Biol ISSN: 0741-5400 Impact factor: 4.962