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• W2078341282 abstract "The current antiretroviral therapy (ART) can effectively reduce plasma HIV loads to undetectable levels, but cannot eliminate latently infected resting memory CD4 T cells that persist for the lifetime of infected patients. Therefore, designing new therapeutic approaches to eliminate these latently infected cells or the cells that produce HIV upon reactivation from latency is a priority in the ART era in order to progress to a cure of HIV. Here, we show that designer T cells expressing chimeric antigen receptor (CAR), CD4-CD28-CD3ζ, can target and kill HIV Env-expressing cells. Further, they secrete effector cytokines upon contact with HIV Env+ target cells that can reactivate latent HIV in a cell line model, thereby exposing those cells to recognition and killing by anti-HIV CAR+ T cells. Taken to the limit, this process could form the basis for an eventual functional or sterilizing cure for HIV in patients." @default.
• W2078341282 created "2016-06-24" @default.
• W2078341282 creator A5020704644 @default.
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• W2078341282 date "2013-11-01" @default.
• W2078341282 modified "2023-10-07" @default.
• W2078341282 title "Anti-HIV designer T cells progressively eradicate a latently infected cell line by sequentially inducing HIV reactivation then killing the newly gp120-positive cells" @default.
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• W2078341282 doi "https://doi.org/10.1016/j.virol.2013.08.002" @default.
• W2078341282 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3791854" @default.
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• W2078341282 hasPublicationYear "2013" @default.
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