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Attacking Latent HIV with convertibleCAR-T Cells, a Highly Adaptable Killing Platform
Author(s) -
Eytan Herzig,
Kaman Chan Kim,
Thomas Packard,
Noam Vardi,
Roland Schwarzer,
Andrea Gramatica,
Steven G. Deeks,
Steven R. Williams,
Kyle E. Landgraf,
Nigel Killeen,
David W. Martin,
Leor S. Weinberger,
Warner C. Greene
Publication year - 2019
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2019.10.002
Subject(s) - biology , human immunodeficiency virus (hiv) , virology , computational biology , microbiology and biotechnology , genetics
Current approaches to reducing the latent HIV reservoir entail first reactivating virus-containing cells to become visible to the immune system. A critical second step is killing these cells to reduce reservoir size. Endogenous cytotoxic T-lymphocytes (CTLs) may not be adequate because of cellular exhaustion and the evolution of CTL-resistant viruses. We have designed a universal CAR-T cell platform based on CTLs engineered to bind a variety of broadly neutralizing anti-HIV antibodies. We show that this platform, convertibleCAR-T cells, effectively kills HIV-infected, but not uninfected, CD4 T cells from blood, tonsil, or spleen and only when armed with anti-HIV antibodies. convertibleCAR-T cells also kill within 48 h more than half of the inducible reservoir found in blood of HIV-infected individuals on antiretroviral therapy. The modularity of convertibleCAR-T cell system, which allows multiplexing with several anti-HIV antibodies yielding greater breadth and control, makes it a promising tool for attacking the latent HIV reservoir.

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