IL-9 is associated with an impaired Th1 immune response in patients with tuberculosis

被引:58
作者
Wu, Bo [1 ]
Huang, Chunhong [1 ]
Kato-Maeda, Midori [2 ]
Hopewell, Philip C. [2 ]
Daley, Charles L. [2 ,3 ]
Krensky, Alan M. [1 ]
Clayberger, Carol [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Pediat, Stanford, CA 94305 USA
[2] Univ Calif San Francisco, Div Pulm & Crit Care Med, San Francisco, CA 94110 USA
[3] Natl Jewish Med & Res Ctr, Div Mycobacterial & Respirat Infect, Denver, CO 80206 USA
关键词
cytokines; mycobacterium tuberculosis; dendritic cell; human;
D O I
10.1016/j.clim.2007.09.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although a defective Th1 response has been demonstrated in patients infected with Mycobacterium tuberculosis (Mtb), the mechanisms leading to this defect are not well understood. To study the immune response to Mtb infection, we stimulated PBMC from individuals with latent tuberculosis infection (LTBI) or patients with tuberculosis (TB) with the Mtb specific antigen early secretory antigenic target-6 (ESAT-6). mRNAs for a panel of cytokines were measured using quantitative real-time PCR (qPCR). PBMC from TB patients exhibited low levels of IFN-gamma, IL-12 alpha, IL-12 beta, and IL-23 mRNA but high levels of IL-9 mRNA. Sera from TB patients blocked the differentiation and function of dendritic cells from TST negative (TST-) donors. Exogenous IL-9 reduced IFN-gamma mRNA expression in PBMC from LTBI by 30% (n=4) and neutralization of IL-9 restored the IFN-gamma mRNA expression in PBMC from TB patients by 66% (n = 8). Thus, increased expression of IL-9 may contribute to the development of TB. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:202 / 210
页数:9
相关论文
共 39 条
[31]  
SANCHEZ FO, 1994, INFECT IMMUN, V62, P5673
[32]   Type 2 cytokine gene activation and its relationship to extent of disease in patients with tuberculosis [J].
Seah, GT ;
Scott, GM ;
Rook, GAW .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (01) :385-389
[33]  
Seah GT, 2001, SCAND J INFECT DIS, V33, P106, DOI 10.1080/003655401750065472
[34]   CCR8 expression identifies CD4 memory T cells enriched for FOXP3+ regulatory and Th2 effector lymphocytes [J].
Soler, Dulce ;
Chapman, Tobias R. ;
Poisson, Louis R. ;
Wang, Lin ;
Cote-Sierra, Javier ;
Ryan, Mark ;
McDonald, Alice ;
Badola, Sunita ;
Fedyk, Eric ;
Coyle, Anthony J. ;
Hodge, Martin R. ;
Kolbeck, Roland .
JOURNAL OF IMMUNOLOGY, 2006, 177 (10) :6940-6951
[35]   Type 1 type 2 immunity in infectious diseases [J].
Spellberg, B ;
Edwards, JE .
CLINICAL INFECTIOUS DISEASES, 2001, 32 (01) :76-102
[36]  
SURCEL HM, 1994, IMMUNOLOGY, V81, P171
[37]   Immunology - What does it mean to be just 17? [J].
Tato, CM ;
O'Shea, JJ .
NATURE, 2006, 441 (7090) :166-168
[38]   Innate immunity to Mycobacterium tuberculosis [J].
van Crevel, R ;
Ottenhoff, THM ;
van der Meer, JWM .
CLINICAL MICROBIOLOGY REVIEWS, 2002, 15 (02) :294-+
[39]   Messenger RNA expression of IL-8, FOXP3, and IL-12β differentiates latent tuberculosis infection from disease [J].
Wu, Bo ;
Huang, Chunhong ;
Kato-Maeda, Midori ;
Hopewell, Philip C. ;
Daley, Charles L. ;
Krensky, Alan M. ;
Clayberger, Carol .
JOURNAL OF IMMUNOLOGY, 2007, 178 (06) :3688-3694