iScience (Jan 2021)

Memory CD8+ T cell heterogeneity is primarily driven by pathogen-specific cues and additionally shaped by the tissue environment

  • Esmé T.I. van der Gracht,
  • Guillaume Beyrend,
  • Tamim Abdelaal,
  • Iris N. Pardieck,
  • Thomas H. Wesselink,
  • Floortje J. van Haften,
  • Suzanne van Duikeren,
  • Frits Koning,
  • Ramon Arens

Journal volume & issue
Vol. 24, no. 1
p. 101954

Abstract

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Summary: Factors that govern the complex formation of memory T cells are not completely understood. A better understanding of the development of memory T cell heterogeneity is however required to enhance vaccination and immunotherapy approaches. Here we examined the impact of pathogen- and tissue-specific cues on memory CD8+ T cell heterogeneity using high-dimensional single-cell mass cytometry and a tailored bioinformatics pipeline. We identified distinct populations of pathogen-specific CD8+ T cells that uniquely connected to a specific pathogen or associated to multiple types of acute and persistent infections. In addition, the tissue environment shaped the memory CD8+ T cell heterogeneity, albeit to a lesser extent than infection. The programming of memory CD8+ T cell differentiation during acute infection is eventually superseded by persistent infection. Thus, the plethora of distinct memory CD8+ T cell subsets that arise upon infection is dominantly sculpted by the pathogen-specific cues and further shaped by the tissue environment.

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