CXCR4-Using HIV Strains Predominate in Naive and Central Memory CD4 + T Cells in People Living with HIV on Antiretroviral Therapy: Implications for How Latency Is Established and Maintained

Author:

Roche Michael12,Tumpach Carolin12,Symons Jori1,Gartner Matthew2,Anderson Jenny L.1,Khoury Gabriela1,Cashin Kieran2,Cameron Paul U.13ORCID,Churchill Melissa J.2,Deeks Steven G.4,Gorry Paul R.2,Lewin Sharon R.13

Affiliation:

1. The Peter Doherty Institute for Infection and Immunity, University of Melbourne and Royal Melbourne Hospital, Melbourne, Australia

2. School of Health and Biomedical Sciences, RMIT University, Bundoora, Australia

3. Department of Infectious Diseases, Monash University and Alfred Hospital, Melbourne, Australia

4. Department of Medicine, University of California, San Francisco, California, USA

Abstract

In people living with HIV (PLWH) on suppressive ART, latent HIV can be found in a diverse range of CD4 + T cells, including quiescent naive and central memory cells that are typically difficult to infect in vitro . It is currently unclear how latency is established in these cells in vivo . We show that in CD4 + T cells from PLWH on suppressive ART, the use of the coreceptor CXCR4 was prevalent among viruses amplified from naive and central memory CD4 + T cells. Furthermore, we found that expanded numbers of identical viral sequences were most common in the effector memory population, and these identical sequences were also found in multiple different CD4 + T cell subsets. Our results help to shed light on how a range of CD4 + T cell subsets come to harbor HIV DNA, which is one of the major barriers to eradicating the virus from PLWH.

Funder

amfAR, The Foundation for AIDS Research

Department of Health | National Health and Medical Research Council

Delaney AIDS Research Enterprise

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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