A unique role for IL-23 in promoting cellular immunity

被引:171
作者
Lankford, CSR [1 ]
Frucht, DM [1 ]
机构
[1] US FDA, DMA, CBER, Cell Biol Lab, Bethesda, MD 20892 USA
关键词
IL-23R; IL-12; IL-12R; Stat4;
D O I
10.1189/jlb.0602326
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent discoveries of interleukin (IL)-23, its receptor, and its signal-transduction pathway add to our understanding of cellular immunity. IL-23 is a heterodimer, comprising IL-12 p40 and the recently cloned IL-23-specific p19 subunit. IL-23 uses many of the same signal-transduction components as IL-12, including IL-12Rbeta1, Janus kinase 2, Tyk2, signal transducer and activator of transcription (Stat)1, Stat3, Stat4, and Stat5. This may explain the similar actions of IL-12 and IL-23 in promoting cellular immunity by inducing interferon-gamma production and proliferative responses in target cells. Additionally, both cytokines promote the T helper cell type 1 costimulatory function of antigen-presenting cells. IL-23 does differ from IL-12 in the T cell subsets that it targets. Whereas IL-12 acts on naive CD4(+) T cells, IL-23 preferentially acts on memory CD4(+) T cells. This review summarizes recent advances regarding IL-23, providing a functional and mechanistic basis for the unique niche that IL-23 occupies in cellular immunity.
引用
收藏
页码:49 / 56
页数:8
相关论文
共 43 条
[1]   Impairment of mycobacterial immunity in human interleukin-12 receptor deficiency [J].
Altare, F ;
Durandy, A ;
Lammas, D ;
Emile, JF ;
Lamhamedi, S ;
Le Deist, F ;
Drysdale, P ;
Jouanguy, E ;
Döffinger, R ;
Bernaudin, F ;
Jeppsson, O ;
Gollob, JA ;
Meinl, E ;
Segal, AW ;
Fischer, A ;
Kumararatne, D ;
Casanova, JL .
SCIENCE, 1998, 280 (5368) :1432-1435
[2]   INTERLEUKIN-12 INDUCES TYROSINE PHOSPHORYLATION AND ACTIVATION OF STAT4 IN HUMAN-LYMPHOCYTES [J].
BACON, CM ;
PETRICOIN, EF ;
ORTALDO, JR ;
REES, RC ;
LARNER, AC ;
JOHNSTON, JA ;
O'SHEA, JJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7307-7311
[3]   IL-23 and IL-12 have overlapping, but distinct, effects on murine dendritic cells [J].
Belladonna, ML ;
Renauld, JC ;
Bianchi, R ;
Vacca, C ;
Fallarino, F ;
Orabona, C ;
Fioretti, MC ;
Grohmann, U ;
Puccetti, P .
JOURNAL OF IMMUNOLOGY, 2002, 168 (11) :5448-5454
[4]  
Camoglio L, 2002, EUR J IMMUNOL, V32, P261, DOI 10.1002/1521-4141(200201)32:1<261::AID-IMMU261>3.0.CO
[5]  
2-X
[6]   Development of Th1-type immune responses requires the type I cytokine receptor TCCR [J].
Chen, Q ;
Ghilardi, N ;
Wang, H ;
Baker, T ;
Xie, MH ;
Gurney, A ;
Grewal, IS ;
de Sauvage, FJ .
NATURE, 2000, 407 (6806) :916-920
[7]  
Cho SS, 1996, J IMMUNOL, V157, P4781
[8]   Mice lacking bioactive IL-12 can generate protective, antigen-specific cellular responses to mycobacterial infection only if the IL-12 p40 subunit is present [J].
Cooper, AM ;
Kipnis, A ;
Turner, J ;
Magram, J ;
Ferrante, J ;
Orme, IM .
JOURNAL OF IMMUNOLOGY, 2002, 168 (03) :1322-1327
[9]   STATs and gene regulation [J].
Darnell, JE .
SCIENCE, 1997, 277 (5332) :1630-1635
[10]  
de Jong R, 1998, SCIENCE, V280, P1435