Relationship between CD4 regulatory T cells and anergy in vivo

Lokesh A. Kalekar, Daniel L Mueller

Research output: Contribution to journalReview articlepeer-review

30 Scopus citations

Abstract

Selective suppression of effector CD4+ T cell functions is necessary to prevent immune cell-mediated damage to healthy tissues. This appears especially true during pregnancy or in individuals predisposed to autoimmunity. Foxp3+ regulatory T (Treg) cells and induction of anergy, an acquired state of T cell functional unresponsiveness in Foxp32 cells, have both been implicated as mechanisms to suppress dangerous immune responses to tissue-restricted self-Ags. Anergic CD4+ T cells and Treg cells share a number of phenotypic and mechanistic traits-including the expression of CD73 and folate receptor 4, and the epigenetic modification of Treg cell signature genes-and an interesting relationship between these two subsets has recently emerged. In this review, we will compare and contrast these two subsets, as well as explore the role of anergy in the generation of peripheral Treg cells.

Original languageEnglish (US)
Pages (from-to)2527-2533
Number of pages7
JournalJournal of Immunology
Volume198
Issue number7
DOIs
StatePublished - Apr 1 2017

Bibliographical note

Funding Information:
This work was supported by a Within Our Reach: Finding a Cure for Rheumatoid Arthritis campaign grant from the Rheumatology Research Foundation and by National Institutes of Health Grant P01 AI35296.

Publisher Copyright:
Copyright © 2017 by The American Association of Immunologists, Inc.

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