Journal article

Persistence of envelopes in different CD4 T-cell subsets in antiretroviral therapy-suppressed people with HIV

MJ Gartner, C Tumpach, A Dantanarayana, J Stern, JM Zerbato, JJ Chang, TA Angelovich, JL Anderson, J Symons, SG Deeks, JK Flynn, SR Lewin, MJ Churchill, PR Gorry, M Roche

AIDS | LIPPINCOTT WILLIAMS & WILKINS | Published : 2023

Abstract

Objectives: Despite suppressive antiretroviral therapy (ART), HIV can persist in a diverse range of CD4+ T-cell subsets. Through longitudinal env sampling from people with HIV (PWH) on ART, we characterized the persistence and phenotypic properties of HIV envs over two time-points (T1 and T2). Methods: Longitudinal blood and lymphoid tissue samples were obtained from eight PWH on suppressive ART. Single genome amplification (SGA) was performed on env to understand the genetic diversity and degree of clonal expansions over time. A subset of envs were used to generate pseudovirus particles to assess sensitivity to autologous plasma IgG and broadly neutralizing antibodies (bNAbs). Results: Iden..

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Grants

Awarded by National Institutes of Health


Funding Acknowledgements

This study was supported by a grant from amfAR, The Foundation for AIDS Research (109114-57-RGRL) to M.R. M.G. was supported by an Australian Research Training Program Award from RMIT University. J.K.F. and T.A.A. were supported by RMIT Vice Chancellor Postdoctoral Fellowships. M.R. was supported by an NHMRC Early Career Fellowship. S.R.L. is an NHMRC practitioner fellow and is supported by the National Institutes of Health(NIH) Delaney AIDS Research Enterprise (DARE U19AI096109 and UM1 AI126611-01).