Emergence of the Th17 Pathway and Its Role in Host Defense

被引:105
作者
O'Quinn, Darrell B. [1 ]
Palmer, Matthew T. [1 ]
Lee, Yun Kyung [1 ]
Weaver, Casey T. [1 ]
机构
[1] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
来源
ADVANCES IN IMMUNOLOGY, VOL 99 | 2008年 / 99卷
关键词
D O I
10.1016/S0065-2776(08)00605-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recently, a paradigm shift has emerged in T-cell-mediated adaptive immunity. On the heels of the discovery of T cells with immunosuppressive function, so-called regulatory T cells (Tregs), the diversity of effector cells has expanded to include a third helper T cell, termed Th17. The appreciation that Th17 cells are products of a distinct effector pathway depended critically on observations made during investigations of mouse models of autoimmunity, advanced by discovery of the cytokines IL-17 and IL-23. These studies understandably led investigators to highlight the role played by Th17 cells in autoimmunity. Yet while the dysfunctional behavior of this phenotype as a contributor to inflammatory disease remains a central issue, this pathway evolved to meet a need for host protection against potential pathogens. It has become apparent that the Th17 pathway promotes host defense against certain extracellular bacteria and fungi, but more recent studies also implicate a role in protection against some protozoa and viruses. Here we review the experimental history that ultimately uncovered the existence and nature of Th17 cells, and then turn the reader's attention to what is currently known about Th-17 cells as a bulwark against pathogens.
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页码:115 / 163
页数:49
相关论文
共 262 条
[1]  
Aarvak T, 1999, J IMMUNOL, V162, P1246
[2]   Surface phenotype and antigenic specificity of human interleukin 17-producing T helper memory cells [J].
Acosta-Rodriguez, Eva V. ;
Rivino, Laura ;
Geginat, Jens ;
Jarrossay, David ;
Gattorno, Marco ;
Lanzavecchia, Antonio ;
Sallusto, Federica ;
Napolitani, Giorgio .
NATURE IMMUNOLOGY, 2007, 8 (06) :639-646
[3]   Interleukin-12, a key cytokine in Th1-mediated autoimmune diseases [J].
Adorini, L .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1999, 55 (12) :1610-1625
[4]   T-bet is a STAT1-induced regulator of IL-12R expression in naive CD4+ T cells [J].
Afkarian, M ;
Sedy, JR ;
Yang, J ;
Jacobson, NG ;
Cereb, N ;
Yang, SY ;
Murphy, TL ;
Murphy, KM .
NATURE IMMUNOLOGY, 2002, 3 (06) :549-557
[5]   Interleukin-23 promotes a distinct CD4 T cell activation state characterized by the production of interleukin-17 [J].
Aggarwal, S ;
Ghilardi, N ;
Xie, MH ;
de Sauvage, FJ ;
Gurney, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (03) :1910-1914
[6]   TLR3 and TLR7 are involved in expression of IL-23 subunits while TLR3 but not TLR7 is involved in expression of IFN-β by Theiler's virus-infected RAW264.7 cells [J].
Al-Salleeh, Fahd ;
Petro, Thomas M. .
MICROBES AND INFECTION, 2007, 9 (11) :1384-1392
[7]   Host response to Helicobacter pylori infection before initiation of the adaptive immune response [J].
Algood, Holly M. Scott ;
Gallo-Romero, Judith ;
Wilson, Keith T. ;
Peek, Richard M., Jr. ;
Cover, Timothy L. .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2007, 51 (03) :577-586
[8]   ENCEPHALITOGENIC T-CELLS IN THE B10.PL MODEL OF EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS (EAE) ARE OF THE TH-1 LYMPHOKINE SUBTYPE [J].
ANDO, DG ;
CLAYTON, J ;
KONO, D ;
URBAN, JL ;
SERCARZ, EE .
CELLULAR IMMUNOLOGY, 1989, 124 (01) :132-143
[9]   Th17 cells and mucosal host defense [J].
Auja, Shean J. ;
Dubin, Patricia J. ;
Kolls, Jay K. .
SEMINARS IN IMMUNOLOGY, 2007, 19 (06) :377-382
[10]   IL-22 mediates mucosal host defense against Gram-negative bacterial pneumonia [J].
Aujla, Shean J. ;
Chan, Yvonne R. ;
Zheng, Mingquan ;
Fei, Mingjian ;
Askew, David J. ;
Pociask, Derek A. ;
Reinhart, Todd A. ;
McAllister, Florencia ;
Edeal, Jennifer ;
Gaus, Kristi ;
Husain, Shahid ;
Kreindler, James L. ;
Dubin, Patricia J. ;
Pilewski, Joseph M. ;
Myerburg, Mike M. ;
Mason, Carol A. ;
Iwakura, Yoichiro ;
Kolls, Jay K. .
NATURE MEDICINE, 2008, 14 (03) :275-281