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What determines Th2 differentiation, in vitro and in vivo?

期刊

IMMUNOLOGY AND CELL BIOLOGY
卷 88, 期 3, 页码 236-239

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NATURE PUBLISHING GROUP
DOI: 10.1038/icb.2010.2

关键词

IL-4; IL-13; GATA3; Th1/Th2; basophils; STAT5

资金

  1. Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, USA
  2. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [ZIAAI000493] Funding Source: NIH RePORTER

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We have known since 1991 how to induce naive CD4 T cells to differentiate in vitro into Th2 cells and, over the ensuing years, a comprehensive picture of the molecules involved in this important process has emerged. GATA3 and STAT5 are both essential for in vitro differentiation, stimulating naive cells through a process involving induction, which is T-cell receptor (TCR) dependent but interleukin (IL)-4 independent, and commitment, which is IL-4 dependent. Th2 differentiation in vivo appears more complex. GATA3 and probably STAT5 are required in vivo but, at least for certain helminth infections, the IL-4/IL-4Ra/STAT6 pathway is dispensable. The role of thymic stromal lymphopoietin and of low TCR signal strength and the participation of basophils in establishing a Th2-baising in vivo environment have achieved considerable attention. Here I discuss the major players in Th2 differentiation particularly as they may exert their effects in vivo. Immunology and Cell Biology (2010) 88, 236-239; doi: 10.1038/icb.2010.2; published online 16 February 2010

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