Th17 cells in inflammation

被引:71
作者
Kimura, Akihiro [2 ]
Kishimoto, Tadamitsu [1 ]
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, Lab Immune Regulat, Osaka, Japan
[2] Keio Univ, Sch Med, Dept Microbiol & Immunol, Tokyo, Japan
关键词
Th17; IL-6; TGF-beta; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; ARYL-HYDROCARBON RECEPTOR; REGULATORY T-CELLS; COLLAGEN-INDUCED ARTHRITIS; TRANSCRIPTION FACTOR FOXP3; CENTRAL-NERVOUS-SYSTEM; HELPER-CELLS; INTERLEUKIN-17; FAMILY; MULTIPLE-SCLEROSIS; LINEAGE COMMITMENT;
D O I
10.1016/j.intimp.2010.10.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Naive T cells are multipotential precursors that differentiate into various effector subsets, such as T helper type 1 (Th1) and Th2 cells, which are characterized by their distinct functions. The IL-17-producing T helper (Th17) cell has been recently identified as a new subset of the T helper cell and a mediator of inflammation associated with various autoimmune diseases. Although several cytokines participate in Th17 cell development, IL-6 and TGF-beta are key factors for the generation of Th17 cells from naive T cells. On the other hand, IL-6 inhibits TGF-beta-induced regulatory T (Treg) cells, which suppress adaptive T cell responses and prevent autoimmunity. Recent studies suggest that it is an effective approach in the treatment of various autoimmune and inflammatory diseases to normalize the balance between Treg and Th17 cell development. Here, we review the discovery of the Th17 subset, its properties and relationship with several autoimmune diseases. Crown Copyright (c) 2010 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:319 / 322
页数:4
相关论文
共 51 条
[1]  
APETOH L, 2010, NAT IMMUNOL
[2]   Interleukin 27 limits autoimmune encephalomyelitis by suppressing the development of interleukin 17-producing T cells [J].
Batten, Marcel ;
Li, Ji ;
Yi, Sothy ;
Kljavin, Noelyn M. ;
Danilenko, Dimitry M. ;
Lucas, Sophie ;
Lee, James ;
de Sauvage, Frederic J. ;
Ghilardi, Nico .
NATURE IMMUNOLOGY, 2006, 7 (09) :929-936
[3]   Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells [J].
Bettelli, E ;
Carrier, YJ ;
Gao, WD ;
Korn, T ;
Strom, TB ;
Oukka, M ;
Weiner, HL ;
Kuchroo, VK .
NATURE, 2006, 441 (7090) :235-238
[4]   A FUNCTIONAL DICHOTOMY IN CD4+ LYMPHOCYTES-T [J].
BOTTOMLY, K .
IMMUNOLOGY TODAY, 1988, 9 (09) :268-274
[5]   The development of inflammatory TH-17 cells requires interferon-regulatory factor 4 [J].
Bruestle, Anne ;
Heink, Sylvia ;
Huber, Magdalena ;
Rosenplaenter, Christine ;
Stadelmann, Christine ;
Yu, Philipp ;
Arpaia, Enrico ;
Mak, Tak W. ;
Kamradt, Thomas ;
Lohoff, Michael .
NATURE IMMUNOLOGY, 2007, 8 (09) :958-966
[6]   Conversion of peripheral CD4+CD25- naive T cells to CD4+CD25+ regulatory T cells by TGF-β induction of transcription factor Foxp3 [J].
Chen, WJ ;
Jin, WW ;
Hardegen, N ;
Lei, KJ ;
Li, L ;
Marinos, N ;
McGrady, G ;
Wahl, SM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (12) :1875-1886
[7]   Cutting edge:: IFN-γ regulates the induction and expansion of IL-17-producing CD4 T cells during mycobacterial infection [J].
Cruz, Andrea ;
Khader, Shabaana A. ;
Torrado, Egidio ;
Fraga, Alexandra ;
Pearl, John E. ;
Pedrosa, Jorge ;
Cooper, Andrea M. ;
Castro, Antonio G. .
JOURNAL OF IMMUNOLOGY, 2006, 177 (03) :1416-1420
[8]   IL-27 Blocks RORc Expression to Inhibit Lineage Commitment of Th17 Cells [J].
Diveu, Caroline ;
McGeachy, Mandy J. ;
Boniface, Katia ;
Stumhofer, Jason S. ;
Sathe, Manjiri ;
Joyce-Shaikh, Barbara ;
Chen, Yi ;
Tato, Cristina M. ;
McClanahan, Terrill K. ;
Malefyt, Rene de Waal ;
Hunter, Christopher A. ;
Cua, Daniel J. ;
Kastelein, Robert A. .
JOURNAL OF IMMUNOLOGY, 2009, 182 (09) :5748-5756
[9]  
Ferber IA, 1996, J IMMUNOL, V156, P5
[10]   Regulatory T cell lineage specification by the forkhead transcription factor FoxP3 [J].
Fontenot, JD ;
Rasmussen, JP ;
Williams, LM ;
Dooley, JL ;
Farr, AG ;
Rudensky, AY .
IMMUNITY, 2005, 22 (03) :329-341