| Literature DB >> 27265874 |
Shabnum Patel1, R Brad Jones2, Douglas F Nixon2, Catherine M Bollard3.
Abstract
Although antiretroviral therapy (ART) has been successful in controlling HIV infection, it does not provide a permanent cure, requires lifelong treatment, and HIV-positive individuals are left with social concerns such as stigma. The recent application of T cells to treat cancer and viral reactivations post-transplant offers a potential strategy to control HIV infection. It is known that naturally occurring HIV-specific T cells can inhibit HIV initially, but this response is not sustained in the majority of people living with HIV. Genetically modifying T cells to target HIV, resist infection, and persist in the immunosuppressive environment found in chronically infected HIV-positive individuals might provide a therapeutic solution for HIV. This review focuses on successful preclinical studies and current clinical strategies using T-cell therapy to control HIV infection and mediate a functional cure solution.Entities:
Keywords: CRISPR; HDACIs; HIV; ZFN; adoptive T-cell therapy; artificial TCR; chimeric antigen receptors; gene editing
Mesh:
Year: 2016 PMID: 27265874 PMCID: PMC4935558 DOI: 10.1016/j.jcyt.2016.04.007
Source DB: PubMed Journal: Cytotherapy ISSN: 1465-3249 Impact factor: 5.414