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Plasticity of CD4+ T Cell Lineage Differentiation

Journal

IMMUNITY
Volume 30, Issue 5, Pages 646-655

Publisher

CELL PRESS
DOI: 10.1016/j.immuni.2009.05.001

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Funding

  1. Howard Hughes Medical Institute
  2. Sandler Program for Asthma Research
  3. National Multiple Sclerosis Society
  4. Irvington Institute
  5. Cancer Research Institute Fellowship
  6. Helen and Martin Kimmel Center for Stem Cell Biology Award

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The differentiation of naive CD4(+) T cells into lineages with distinct effector functions has been considered to be an irreversible event. T helper type 1 (Th1) cells stably express IFN-gamma, whereas Th2 cells express IL-4. The discovery and investigation of two other CD4(+) T cell subsets, induced regulatory T (iTreg) cells and Th17 cells, has led to a rethinking of the notion that helper T cell subsets represent irreversibly differentiated endpoints. Accumulating evidence suggests that CD4(+) T cells, particularly iTreg and Th17 cells, are more plastic than previously appreciated. It appears that expression of Foxp3 by iTreg cells or IL-17 by Th17 cells may not be stable and that there is a great degree of flexibility in their differentiation options. Here, we will discuss recent findings that demonstrate the plasticity of CD4(+) T cell differentiation and the biological implications of this flexibility.

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