Quarter Century of Anti-HIV CAR T Cells
- PMID: 29500712
- PMCID: PMC5884727
- DOI: 10.1007/s11904-018-0388-x
Quarter Century of Anti-HIV CAR T Cells
Abstract
Purpose of review: A therapy that might cure HIV is a very important goal for the 30-40 million people living with HIV. Chimeric antigen receptor T cells have recently had remarkable success against certain leukemias, and there are reasons to believe they could be successful for HIV. This manuscript summarizes the published research on HIV CAR T cells and reviews the current anti-HIV chimeric antigen receptor strategies.
Recent findings: Research on anti-HIV chimeric antigen receptor T cells has been going on for at least the last 25 years. First- and second-generation anti-HIV chimeric antigen receptors have been developed. First-generation anti-HIV chimeric antigen receptors were studied in clinical trials more than 15 years ago, but did not have meaningful clinical efficacy. There are some reasons to be optimistic about second-generation anti-HIV chimeric antigen receptor T cells, but they have not yet been tested in vivo.
Keywords: Chimeric antigen receptor (CAR); HIV; HIV cure; Review; T cell therapy; Therapy.
Conflict of interest statement
Thor A. Wagner declares a patent PCT/US2015/024876 pending to Seattle Childrens Hospital.
References
-
- Tran AC, Zhang D, Byrn R, Roberts MR. Chimeric zeta-receptors direct human natural killer (NK) effector function to permit killing of NK-resistant tumor cells and HIV-infected T lymphocytes. J Immunol. 1995;155(2):1000–9. - PubMed
-
- Ni Z, Knorr DA, Bendzick L, Allred J, Kaufman DS. Expression of chimeric receptor CD4zeta by natural killer cells derived from human pluripotent stem cells improves in vitro activity but does not enhance suppression of HIV infection in vivo. Stem Cells. 2014;32(4):1021–31. doi: 10.1002/stem.1611. - DOI - PMC - PubMed
-
- Global report: UNAIDS report on the global AIDS epidemic 2012. Joint United Nations Programme on HIV/AIDS (UNAIDS) 2012
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