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Dendritic Cell Regulation of T Helper Cells.
Yin, Xiangyun; Chen, Shuting; Eisenbarth, Stephanie C.
Affiliation
  • Yin X; Department of Laboratory Medicine and Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA; email: stephanie.eisenbarth@yale.edu.
  • Chen S; Department of Laboratory Medicine and Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA; email: stephanie.eisenbarth@yale.edu.
  • Eisenbarth SC; Department of Laboratory Medicine and Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA; email: stephanie.eisenbarth@yale.edu.
Annu Rev Immunol ; 39: 759-790, 2021 04 26.
Article in En | MEDLINE | ID: mdl-33710920
ABSTRACT
As the professional antigen-presenting cells of the immune system, dendritic cells (DCs) sense the microenvironment and shape the ensuing adaptive immune response. DCs can induce both immune activation and immune tolerance according to the peripheral cues. Recent work has established that DCs comprise several phenotypically and functionally heterogeneous subsets that differentially regulate T lymphocyte differentiation. This review summarizes both mouse and human DC subset phenotypes, development, diversification, and function. We focus on advances in our understanding of how different DC subsets regulate distinct CD4+ T helper (Th) cell differentiation outcomes, including Th1, Th2, Th17, T follicular helper, and T regulatory cells. We review DC subset intrinsic properties, local tissue microenvironments, and other immune cells that together determine Th cell differentiation during homeostasis and inflammation.
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Full text: 1 Database: MEDLINE Main subject: Lymphocyte Activation / Immune Tolerance Limits: Animals / Humans Language: En Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: Lymphocyte Activation / Immune Tolerance Limits: Animals / Humans Language: En Year: 2021 Type: Article