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Science 325 (5943): 953-955

Copyright © 2009 by the American Association for the Advancement of Science

Immunology

The Yin and Yang of Follicular Helper T Cells

Amit Awasthi, and Vijay K. Kuchroo

The human immune system can harness an arsenal of lymphocytes called CD4+ T cells, in an adaptive response to infection by a variety of pathogens, including parasites, bacteria, and fungi. Once activated, CD4+ T cells can differentiate into subsets of helper T cells [TH1, TH2, TH17, regulatory T (Treg), and follicular T (TFH)], whose effector functions include secreting the cytokines necessary for clearing pathogens and inducing inflammatory responses. Each helper T cell subtype is also critical for helping B lymphocytes produce pathogen-specific antibodies (1). Until now, master transcription factors have been identified that regulate the generation of helper T cell lineages except for TFH cells. On pages 1006 and 1001 of this issue, Johnston et al. (2) and Nurieva et al. (3), and a study by Yu et al. (4), report that the transcription factor Bcl6 is a master transcription factor that controls the generation of TFH cells. However, Bcl6 must work against another transcription factor, Blimp-1, to promote this differentiation process.

Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.

E-mail: vkuchroo{at}rics.bwh.harvard.edu

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
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