Cell Reports (Nov 2014)

CD161 Defines a Transcriptional and Functional Phenotype across Distinct Human T Cell Lineages

  • Joannah R. Fergusson,
  • Kira E. Smith,
  • Vicki M. Fleming,
  • Neil Rajoriya,
  • Evan W. Newell,
  • Ruth Simmons,
  • Emanuele Marchi,
  • Sophia Björkander,
  • Yu-Hoi Kang,
  • Leo Swadling,
  • Ayako Kurioka,
  • Natasha Sahgal,
  • Helen Lockstone,
  • Dilair Baban,
  • Gordon J. Freeman,
  • Eva Sverremark-Ekström,
  • Mark M. Davis,
  • Miles P. Davenport,
  • Vanessa Venturi,
  • James E. Ussher,
  • Christian B. Willberg,
  • Paul Klenerman

DOI
https://doi.org/10.1016/j.celrep.2014.09.045
Journal volume & issue
Vol. 9, no. 3
pp. 1075 – 1088

Abstract

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The C-type lectin CD161 is expressed by a large proportion of human T lymphocytes of all lineages, including a population known as mucosal-associated invariant T (MAIT) cells. To understand whether different T cell subsets expressing CD161 have similar properties, we examined these populations in parallel using mass cytometry and mRNA microarray approaches. The analysis identified a conserved CD161++/MAIT cell transcriptional signature enriched in CD161+CD8+ T cells, which can be extended to CD161+ CD4+ and CD161+TCRγδ+ T cells. Furthermore, this led to the identification of a shared innate-like, TCR-independent response to interleukin (IL)-12 plus IL-18 by different CD161-expressing T cell populations. This response was independent of regulation by CD161, which acted as a costimulatory molecule in the context of T cell receptor stimulation. Expression of CD161 hence identifies a transcriptional and functional phenotype, shared across human T lymphocytes and independent of both T cell receptor (TCR) expression and cell lineage.