CD32(+)CD4(+) memory T cells are enriched for total HIV-1 DNA in tissues from humanized mice

  • Philipp Alexander Adams
  • , Virginie Fievez
  • , Rafaela Schober
  • , Mathieu Amand
  • , Gilles Iserentant
  • , Sofie Rutsaert
  • , Geraldine Dessilly
  • , Guido Vanham
  • , Fanny Hedin
  • , Antonio Cosma
  • , Michel Moutschen
  • , Linos Vandekerckhove
  • , Carole Seguin-Devaux

Research output: Contribution to journalA1: Web of Science-articlepeer-review

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Abstract

CD32 has raised conflicting results as a putative marker of the HIV-1 reservoir. We measured CD32 expression in tissues from viremic and virally suppressed humanized mice treated relatively early or late after HIV-1 infection with combined antiretroviral therapy. CD32 was expressed in a small fraction of the memory CD4(+) T-cell subsets from different tissues in viremic and aviremic mice, regardless of treatment initiation time. CD32(+) memory CD4(+) T cells were enriched in cell associated (CA) HIV-1 DNA but not in CA HIV-1 RNA as compared to the CD32(-) CD4(+) fraction. Using multidimensional reduction analysis, several memory CD4(+)CD32(+) T-cell clusters were identified expressing HLA-DR, TIGIT, or PD-1. Importantly, although tissue-resident CD32(+)CD4(+) memory cells were enriched with translation-competent reservoirs, most of it was detected in memory CD32-CD4(+) T cells. Our findings support that CD32 labels highly activated/exhausted memory CD4(+) T-cell subsets that contain only a small proportion of the translation-competent reservoir.

Original languageEnglish
Article number101881
JournalIscience
Volume24
Issue number1
Number of pages33
DOIs
Publication statusPublished - 2021

Keywords

  • ANTIRETROVIRAL THERAPY
  • LATENT RESERVOIR
  • INFECTED INDIVIDUALS
  • IMMUNE ACTIVATION
  • ANTIVIRAL THERAPY
  • CD4(+)
  • REPLICATION
  • PERSISTENCE
  • EXPRESSION
  • BLOOD

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