Th2 Cells in Health and Disease

Author:

Nakayama Toshinori12,Hirahara Kiyoshi1,Onodera Atsushi13,Endo Yusuke1,Hosokawa Hiroyuki1,Shinoda Kenta1,Tumes Damon J.14,Okamoto Yoshitaka5

Affiliation:

1. Department of Immunology, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan;, , , , , , ,

2. AMED-CREST, AMED, Chiba 260-8670, Japan

3. Institute for Global Prominent Research, Chiba University, Chiba 260-8670, Japan

4. South Australian Health and Medical Research Institute, North Terrace, Adelaide SA 5000, Australia

5. Department of Otorhinolaryngology, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan

Abstract

Helper T (Th) cell subsets direct immune responses by producing signature cytokines. Th2 cells produce IL-4, IL-5, and IL-13, which are important in humoral immunity and protection from helminth infection and are central to the pathogenesis of many allergic inflammatory diseases. Molecular analysis of Th2 cell differentiation and maintenance of function has led to recent discoveries that have refined our understanding of Th2 cell biology. Epigenetic regulation of Gata3 expression by chromatin remodeling complexes such as Polycomb and Trithorax is crucial for maintaining Th2 cell identity. In the context of allergic diseases, memory-type pathogenic Th2 cells have been identified in both mice and humans. To better understand these disease-driving cell populations, we have developed a model called the pathogenic Th population disease induction model. The concept of defined subsets of pathogenic Th cells may spur new, effective strategies for treating intractable chronic inflammatory disorders.

Publisher

Annual Reviews

Subject

Immunology,Immunology and Allergy

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