Journal article
The pathway to establishing HIV latency is critical to how latency is maintained and reversed
SD Rezaei, HK Lu, J Judy Chang, A Rhodes, SR Lewin, PU Cameron
Journal of Virology | AMER SOC MICROBIOLOGY | Published : 2018
DOI: 10.1128/JVI.02225-17
Abstract
HIV infection requires lifelong antiretroviral therapy because of the persistence of latently infected CD4+ T cells. The induction of virus expression from latently infected cells occurs following T cell receptor (TCR) activation, but not all latently infected cells respond to TCR stimulation. We compared two models of latently infected cells using an enhanced green fluorescent protein (EGFP) reporter virus to infect CCL19-treated resting CD4+ (rCD4+) T cells (preactivation latency) or activated CD4+ T cells that returned to a resting state (postactivation latency). We isolated latently infected cells by sorting for EGFP-negative (EGFP-) cells after infection. These cells were cultured with ..
View full abstractGrants
Awarded by National Institutes of Health
Funding Acknowledgements
This work was supported by NHMRC project grant APP1058891. S.R.L. and P.U.C. are supported by the Division of AIDS, National Institute of Allergy and Infectious Diseases, U.S. National Institutes of Health (Delaney AIDS Research Enterprise [DARE]; U19AI096109). S.R.L. was supported by a NHMRC practitioner fellowship. S.D.R. was the recipient of an Australian postgraduate award.