VISTA is a checkpoint regulator for naïve T cell quiescence and peripheral tolerance

Mohamed ElTanbouly(Dartmouth College), Yanding Zhao(Dartmouth College), Elizabeth C. Nowak(Dartmouth College), Jiannan Li(Adimab (United States)), Evelien Schaafsma(Dartmouth College), Isabelle Le Mercier(Q Therapeutics (United States)), Sabrina Ceeraz(Springhouse), J. Louise Lines(Dartmouth College), Changwei Peng(University of Minnesota), Catherine Carrière(ImmuNext (United States)), Xin Huang(ImmuNext (United States)), Maria Day(ImmuNext (United States)), Brent H. Koehn(University of Minnesota), Sam W. Lee(Yale University), Milagros Silva Morales(University of Minnesota Medical Center), Kristin A. Hogquist(University of Minnesota), Stephen C. Jameson(University of Minnesota), Daniel L. Mueller(University of Minnesota), Jay L. Rothstein(ImmuNext (United States)), Bruce R. Blazar(University of Minnesota), Chao Cheng(Dartmouth College), Randolph J. Noelle(Dartmouth College)
Science
January 16, 2020
Cited by 281Open Access
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Abstract

Negative checkpoint regulators (NCRs) temper the T cell immune response to self-antigens and limit the development of autoimmunity. Unlike all other NCRs that are expressed on activated T lymphocytes, V-type immunoglobulin domain-containing suppressor of T cell activation (VISTA) is expressed on naïve T cells. We report an unexpected heterogeneity within the naïve T cell compartment in mice, where loss of VISTA disrupted the major quiescent naïve T cell subset and enhanced self-reactivity. Agonistic VISTA engagement increased T cell tolerance by promoting antigen-induced peripheral T cell deletion. Although a critical player in naïve T cell homeostasis, the ability of VISTA to restrain naïve T cell responses was lost under inflammatory conditions. VISTA is therefore a distinctive NCR of naïve T cells that is critical for steady-state maintenance of quiescence and peripheral tolerance.


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