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

Joannah R. Fergusson(University of Oxford), Kira Smith(Medawar Building for Pathogen Research), Vicki M. Fleming(Oxford University Hospitals NHS Trust), Neil Rajoriya(Medawar Building for Pathogen Research), Evan W. Newell(Stanford University), Ruth Simmons(Medawar Building for Pathogen Research), Emanuele Marchi(Medawar Building for Pathogen Research), Sophia Björkander(Stockholm University), Yu-Hoi Kang(University of Oxford), Leo Swadling(Medawar Building for Pathogen Research), Ayako Kurioka(Medawar Building for Pathogen Research), Natasha Sahgal(Centre for Human Genetics), Helen Lockstone(Centre for Human Genetics), Dilair Baban(University of Oxford), Gordon J. Freeman(Dana-Farber Cancer Institute), Eva Sverremark‐Ekström(Stockholm University), Mark M. Davis(Stanford University), Miles P. Davenport(Prince of Wales Hospital), Vanessa Venturi(Prince of Wales Hospital), James E. Ussher(University of Otago), Christian B. Willberg(University of Oxford), Paul Klenerman(Medawar Building for Pathogen Research)
Cell Reports
October 24, 2014
Cited by 320Open Access
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Abstract

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.


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