Unique phenotypes and clonal expansions of human CD4 effector memory T cells re-expressing CD45RA

Yuan Tian(La Jolla Institute for Immunology), Mariana Babor(La Jolla Institute for Immunology), Jerome C. Lane(La Jolla Institute for Immunology), Véronique Schulten(La Jolla Institute for Immunology), Veena S. Patil(La Jolla Institute for Immunology), Grégory Seumois(La Jolla Institute for Immunology), Sandy L. Rosales(La Jolla Institute for Immunology), Zheng Fu(La Jolla Institute for Immunology), Gaëlle Picarda(La Jolla Institute for Immunology), Julie G. Burel(La Jolla Institute for Immunology), Jose Zapardiel‐Gonzalo(La Jolla Institute for Immunology), Rashika N. Tennekoon(La Jolla Institute for Immunology), Aruna Dharshan De Silva(La Jolla Institute for Immunology), Sunil Premawansa(University of Colombo), Gayani Premawansa(Colombo North Teaching Hospital), Ananda Wijewickrama, Jason Greenbaum(La Jolla Institute for Immunology), Pandurangan Vijayanand(La Jolla Institute for Immunology), Daniela Weiskopf(La Jolla Institute for Immunology), Alessandro Sette(La Jolla Institute for Immunology), Bjoern Peters(La Jolla Institute for Immunology)
Nature Communications
November 7, 2017
Cited by 280Open Access
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Abstract

Abstract The expression of CD45RA is generally associated with naive T cells. However, a subset of effector memory T cells re-expresses CD45RA (termed TEMRA) after antigenic stimulation with unknown molecular characteristics and functions. CD4 TEMRA cells have been implicated in protective immunity against pathogens such as dengue virus (DENV). Here we show that not only the frequency but also the phenotype of CD4 TEMRA cells are heterogeneous between individuals. These cells can be subdivided into two major subsets based on the expression of the adhesion G protein-coupled receptor GPR56, and GPR56 + TEMRA cells display a transcriptional and proteomic program with cytotoxic features that is distinct from effector memory T cells. Moreover, GPR56 + TEMRA cells have higher levels of clonal expansion and contain the majority of virus-specific TEMRA cells. Overall, this study reveals the heterogeneity of CD4 TEMRA cells and provides insights into T-cell responses against DENV and other viral pathogens.


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