Literature DB >> 25138734

A novel real-time CTL assay to measure designer T-cell function against HIV Env(+) cells.

Andrew G MacLean1, Edith Walker, Gautam K Sahu, Gail Skowron, Preston Marx, Dorothee von Laer, Richard P Junghans, Stephen E Braun.   

Abstract

BACKGROUND: To increase the immunosurveillance in HIV infection, we used retroviral vectors expressing CD4-chimeric antigen receptors (CARs) to genetically modify autologous T cells and redirect CTL toward HIV. The CD4 extracellular domain targets envelope and the intracellular signaling domains activate T cells. The maC46 fusion inhibitor binds HIV and blocks viral replication.
METHODS: We stimulated rhesus PBMCs with antibodies to CD3/CD28 and cotransduced T cells with CD4-CAR and maC46 vectors. CD4-CAR-transduced T cells were added to Env(+) 293T cells at E:T of 1:1. Killing of target cells was measured as reduced impedance.
RESULTS: We observed gene expression in 60-70% of rhesus CD3(+) CD8(+) T cells with the individual vectors and in 35% of the cells with both vectors. CD4-CAR-transduced populations specifically killed Env(+) cells.
CONCLUSIONS: In these studies, we showed that designer T cells were redirected to kill Env(+) cells. Control of viremia without HAART would revolutionize treatment for HIV patients.
© 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  CD4-CAR; cytotoxic T lymphocytes; dTc; maC46; rhesus macaque; transduced T cells

Mesh:

Substances:

Year:  2014        PMID: 25138734      PMCID: PMC4318253          DOI: 10.1111/jmp.12137

Source DB:  PubMed          Journal:  J Med Primatol        ISSN: 0047-2565            Impact factor:   0.667


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