Journal article

Persistence of integrated HIV DNA in CXCR3 CCR6 memory CD4R T cells in HIV-infected individuals on antiretroviral therapy

G Khoury, JL Anderson, R Fromentin, W Hartogenesis, MZ Smith, P Bacchetti, FM Hecht, N Chomont, PU Cameron, SG Deeks, SR Lewin

AIDS | Published : 2016

Abstract

Background: HIV latent infection can be established in vitro by treating resting CD4+ T cells with chemokines that bind to chemokine receptors (CKR), CCR7, CXCR3, and CCR6, highly expressed on T cells. Objective: To determine if CKR identify CD4+ T cells enriched for HIV in HIV-infected individuals receiving suppressive antiretroviral therapy (ART). Design: A cross-sectional study of CKR expression and HIV persistence in blood from HIV-infected individuals on suppressive ART for more than 3 years (n=48). A subset of 20 individuals underwent leukapheresis and sorting of specific CD4+ T-cell subsets. Methods: We used flow cytometry to quantify CCR5, CCR6, CXCR3, and CXCR5 expression on CD4+ T ..

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University of Melbourne Researchers

Grants

Awarded by National Institute of Allergy and Infectious Diseases


Funding Acknowledgements

The work was supported by the National Institutes of Health Delaney AIDS Research Enterprise (Grant U19 A1096109). G.K. is a recipient of a National Health and Medical Research Council of Australia (NHMRC) Dora Lush biomedical postgraduate scholarship (579719). M.Z.S. is a recipient of an NHMRC Overseas Biomedical Research Fellowship (490988). S.R.L. is an NHMRC practitioner fellow.