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10.1172/JCI95127

http://scihub22266oqcxt.onion/10.1172/JCI95127
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C5873886!5873886!29553486
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suck abstract from ncbi


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pmid29553486      J+Clin+Invest ä ; 128 (4): 1627-40
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  • The anti-caspase inhibitor Q-VD-OPH prevents AIDS disease progression in SIV-infected rhesus macaques #MMPMID29553486
  • Laforge M; Silvestre R; Rodrigues V; Garibal J; Campillo-Gimenez L; Mouhamad S; Monceaux V; Cumont MC; Rabezanahary H; Pruvost A; Cordeiro-da-Silva A; Hurtrel B; Silvestri G; Senik A; Estaquier J
  • J Clin Invest ä[]; 128 (4): 1627-40 PMID29553486show ga
  • Apoptosis has been proposed as a key mechanism responsible for CD4+ T cell depletion and immune dysfunction during HIV infection. We demonstrated that Q-VD-OPH, a caspase inhibitor, inhibits spontaneous and activation-induced death of T cells from SIV-infected rhesus macaques (RMs). When administered during the acute phase of infection, Q-VD-OPH was associated with (a) reduced levels of T cell death, (b) preservation of CD4+/CD8+ T cell ratio in lymphoid organs and in the gut, (c) maintenance of memory CD4+ T cells, and (d) increased specific CD4+ T cell response associated with the expression of cytotoxic molecules. Although therapy was limited to the acute phase of infection, Q-VD-OPH?treated RMs showed lower levels of both viral load and cell-associated SIV DNA as compared with control SIV-infected RMs throughout the chronic phase of infection, and prevented the development of AIDS. Overall, our data demonstrate that Q-VD-OPH injection in SIV-infected RMs may represent an adjunctive therapeutic agent to control HIV infection and delaying disease progression to AIDS.
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