Differential Roles of Interleukin-17A and-17F in Host Defense against Mucoepithelial Bacterial Infection and Allergic Responses

被引:841
作者
Ishigame, Harumichi [1 ]
Kakuta, Shigeru [1 ]
Nagai, Takeshi [2 ]
Kadoki, Motohiko [1 ]
Nambu, Aya [1 ]
Komiyama, Yutaka [1 ]
Fujikado, Noriyuki [1 ]
Tanahashi, Yuko [1 ]
Akitsu, Aoi [1 ]
Kotaki, Hayato [1 ]
Sudo, Katsuko [1 ]
Nakae, Susumu [1 ,3 ]
Sasakawa, Chihiro [2 ]
Iwakura, Yoichiro [1 ,4 ]
机构
[1] Univ Tokyo, Ctr Med Expt, Minato Ku, Inst Med Sci, Tokyo 1088639, Japan
[2] Univ Tokyo, Dept Microbiol & Immun, Minato Ku, Inst Med Sci, Tokyo 1088639, Japan
[3] Univ Tokyo, Frontier Res Initiat, Minato Ku, Inst Med Sci, Tokyo 1088639, Japan
[4] Japan Sci & Technol Agcy, CREST, Kawaguchi, Saitama 3320012, Japan
基金
日本学术振兴会;
关键词
IL-1 RECEPTOR ANTAGONIST; T-HELPER-CELLS; CITROBACTER-RODENTIUM; AUTOIMMUNE ENCEPHALOMYELITIS; IL-17-DEFICIENT MICE; FAMILY-MEMBERS; CUTTING EDGE; TNF-ALPHA; INFLAMMATION; CYTOKINE;
D O I
10.1016/j.immuni.2008.11.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin-17A (IL-17A) is a cytokine produced by T helper 17 (Th17) cells and plays important roles in the development of inflammatory diseases. Although IL-17F is highly homologous to IL-17A and binds the same receptor, the functional roles of this molecule remain largely unknown. Here, we demonstrated with II17a(-/-), II17f(-/-), and II17a(-/-)II17f(-/-) mice that IL-17F played only marginal roles, if at all, in the development of delayed-type and contact hypersensitivities, autoimmune encephalomyelitis, collagen-induced arthritis, and arthritis in II1rn(-/-) mice. In contrast, both IL-17F and IL-17A were involved in host defense against mucoepithelial infection by Staphylococcus aureus and Citrobacter rodentium. IL-17A was produced mainly in T cells, whereas IL-17F was produced in T cells, innate immune cells and epithelial cells. Although only IL-17A efficiently; induced cytokines in macrophages, both cytokines activated epithelial innate immune responses. These observations indicate that IL-17A and IL-17F have overlapping yet distinct roles in host immune and defense mechanisms.
引用
收藏
页码:108 / 119
页数:12
相关论文
共 50 条
[1]  
Antonysamy MA, 1999, J IMMUNOL, V162, P577
[2]   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
[3]   Critical role of T cell-dependent serum antibody, but not the gut-associated lymphoid tissue, for surviving acute mucosal infection with Citrobacter rodentium, an attaching and effacing pathogen [J].
Bry, L ;
Brenner, MB .
JOURNAL OF IMMUNOLOGY, 2004, 172 (01) :433-441
[4]   Langerhans cell histiocytosis reveals a new IL-17A dependent pathway of dendritic cell fusion [J].
Coury, Fabienne ;
Annels, Nicola ;
Rivollier, Aymeric ;
Olsson, Selma ;
Santoro, Alessandra ;
Speziani, Carole ;
Azocar, Olga ;
Flacher, Monique ;
Djebali, Sophia ;
Tebib, Jacques ;
Brytting, Maria ;
Egeler, R. Maarten ;
Rabourdin-Combe, Chantal ;
Henter, Jan-Inge ;
Arico, Maurizio ;
Delprat, Christine .
NATURE MEDICINE, 2008, 14 (01) :81-87
[5]   TLR-2 and IL-17A in chitin-induced macrophage activation and acute inflammation [J].
Da Silva, Carla A. ;
Hartl, Dominik ;
Liu, Wei ;
Lee, Chun G. ;
Elias, Jack A. .
JOURNAL OF IMMUNOLOGY, 2008, 181 (06) :4279-4286
[6]   Divergent roles of IL-23 and IL-12 in host defense against Klebsiella pneumoniae [J].
Happel, KI ;
Dubin, PJ ;
Zheng, MQ ;
Ghilardi, N ;
Lockhart, C ;
Quinton, LJ ;
Odden, AR ;
Shellito, JE ;
Bagby, GJ ;
Nelson, S ;
Kolls, JK .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (06) :761-769
[7]   TNF-α is crucial for the development of autoimmune arthritis in IL-1 receptor antagonist-deficient mice [J].
Horai, R ;
Nakajima, A ;
Habiro, K ;
Kotani, M ;
Nakae, S ;
Matsuki, T ;
Nambu, A ;
Saijo, S ;
Kotaki, H ;
Sudo, K ;
Okahara, A ;
Tanioka, H ;
Ikuse, T ;
Ishii, N ;
Schwartzberg, PL ;
Abe, R ;
Iwakura, Y .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (11) :1603-1611
[8]   Interleukin-23 drives innate and T cell-mediated intestinal inflammation [J].
Hue, Sophie ;
Ahern, Philip ;
Buonocore, Sofia ;
Kullberg, Marika C. ;
Cua, Daniel J. ;
McKenzie, Brent S. ;
Powrie, Fiona ;
Maloy, Kevin J. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2006, 203 (11) :2473-2483
[9]   New IL-17 family members promote Th1 or Th2 responses in the lung: In vivo function of the novel cytokine IL-25 [J].
Hurst, SD ;
Muchamuel, T ;
Gorman, DM ;
Gilbert, JM ;
Clifford, T ;
Kwan, S ;
Menon, S ;
Seymour, B ;
Jackson, C ;
Kung, TT ;
Brieland, JK ;
Zurawski, SM ;
Chapman, RW ;
Zurawski, G ;
Coffman, RL .
JOURNAL OF IMMUNOLOGY, 2002, 169 (01) :443-453
[10]   IL-17s adopt a cystine knot fold: structure and activity of a novel cytokine, IL-17F, and implications for receptor binding [J].
Hymowitz, SG ;
Filvaroff, EH ;
Yin, JP ;
Lee, J ;
Cai, LP ;
Risser, P ;
Maruoka, M ;
Mao, WG ;
Foster, J ;
Kelley, RF ;
Pan, GH ;
Gurney, AL ;
de Vos, AM ;
Starovasnik, MA .
EMBO JOURNAL, 2001, 20 (19) :5332-5341