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Subsets of Tissue CD4 T Cells Display Different Susceptibilities to HIV Infection and Death: Analysis by CyTOF and Single Cell RNA-seq.
Luo, Xiaoyu; Frouard, Julie; Zhang, Gang; Neidleman, Jason; Xie, Guorui; Sheedy, Emma; Roan, Nadia R; Greene, Warner C.
Afiliación
  • Luo X; Gladstone Institute of Virology, San Francisco, CA, United States.
  • Frouard J; Gladstone Institute of Virology, San Francisco, CA, United States.
  • Zhang G; Department of Urology, University of California, San Francisco, San Francisco, CA, United States.
  • Neidleman J; Gladstone Institute of Virology, San Francisco, CA, United States.
  • Xie G; Gladstone Institute of Virology, San Francisco, CA, United States.
  • Sheedy E; Department of Urology, University of California, San Francisco, San Francisco, CA, United States.
  • Roan NR; Gladstone Institute of Virology, San Francisco, CA, United States.
  • Greene WC; Department of Urology, University of California, San Francisco, San Francisco, CA, United States.
Front Immunol ; 13: 883420, 2022.
Article en En | MEDLINE | ID: mdl-35784348
ABSTRACT
CD4 T lymphocytes belong to diverse cellular subsets whose sensitivity or resistance to HIV-associated killing remains to be defined. Working with lymphoid cells from human tonsils, we characterized the HIV-associated depletion of various CD4 T cell subsets using mass cytometry and single-cell RNA-seq. CD4 T cell subsets preferentially killed by HIV are phenotypically distinct from those resistant to HIV-associated cell death, in a manner not fully accounted for by their susceptibility to productive infection. Preferentially-killed subsets express CXCR5 and CXCR4 while preferentially-infected subsets exhibit an activated and exhausted effector memory cell phenotype. Single-cell RNA-seq analysis reveals that the subsets of preferentially-killed cells express genes favoring abortive infection and pyroptosis. These studies emphasize a complex interplay between HIV and distinct tissue-based CD4 T cell subsets, and the important contribution of abortive infection and inflammatory programmed cell death to the overall depletion of CD4 T cells that accompanies untreated HIV infection.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / VIH-1 Límite: Humans Idioma: En Revista: Front Immunol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / VIH-1 Límite: Humans Idioma: En Revista: Front Immunol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos