Differential IL-2 expression defines developmental fates of follicular versus nonfollicular helper T cells

Author:

DiToro Daniel1,Winstead Colleen J.1,Pham Duy1ORCID,Witte Steven1ORCID,Andargachew Rakieb2ORCID,Singer Jeffrey R.1ORCID,Wilson C. Garrett1,Zindl Carlene L.1,Luther Rita J.1ORCID,Silberger Daniel J.1,Weaver Benjamin T.3,Kolawole E. Motunrayo2,Martinez Ryan J.2,Turner Henrietta1,Hatton Robin D.1ORCID,Moon James J.4ORCID,Way Sing Sing5,Evavold Brian D.2ORCID,Weaver Casey T.1ORCID

Affiliation:

1. Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35203, USA.

2. Department of Microbiology and Immunology, Emory University, Atlanta, GA 30322, USA.

3. HudsonAlpha Institute for Biotechnology, Huntsville, AL 35806, USA.

4. Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02129, USA.

5. Division of Infectious Diseases and Perinatal Institute, Cincinnati Children’s Hospital, Cincinnati, OH 45229, USA.

Abstract

(IL-)2 be or not to be? Immunological T follicular helper (T FH ) cells are a subpopulation of CD4 + T cells that support B cell antibody production and the establishment of B cell memory. By contrast, non-T FH cells orchestrate enhanced innate immune cell functions at sites of pathogen encounter. The factors underlying differentiation into a T FH or non-T FH cell remain poorly understood, though there is evidence to suggest that the T cell growth factor interleukin-2 (IL-2) may play a role. Using IL-2 reporter mice, DiToro et al. show that naïve CD4 + T cells that produce IL-2 are fated to become T FH cells, whereas nonproducers, which receive IL-2, become non-T FH cells. The CD4 + T cell–fate decision was linked to T cell receptor strength—only those naïve CD4 + T cells that received the highest T cell receptor signals were able to produce IL-2. Science , this issue p. eaao2933

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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