TH17 (and TH1) signatures of intestinal biopsies of CD patients in response to gliadin

被引:90
作者
Castellanos-Rubio, Ainara [1 ]
Santin, Izortze [1 ]
Irastorza, Inaki [2 ]
Castano, Luis [1 ,3 ]
Carlos Vitoria, Juan [2 ,3 ]
Ramon Bilbao, Jose [1 ,4 ]
机构
[1] Hosp Cruces, Endocrinol Diabet & Nutr Res Grp, Immunogenet Lab, E-48903 Baracaldo, Bizkaia, Spain
[2] Hosp Cruces, Pediat Gastroenterol Unit, Baracaldo, Spain
[3] Univ Basque Country, Dept Pediat, Bilbao, Spain
[4] Univ Basque Country, Dept Genet Anim Physiol & Phys Anthropol, Bilbao, Spain
关键词
Celiac disease; intestinal biopsy; Th17; response; Th1; interleukins; DISEASE; EXPRESSION; INDUCTION; MUCOSA; MICA;
D O I
10.1080/08916930802350789
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Celiac disease (CD) is an immunological disorder caused by intolerance to ingested gliadin and other cereal prolamins that has been included in the TH1-dominated group of diseases, where IL-12 induced IFN is the major proinflamatory signal. Recently, another linage of T cells has been described, namely TH17, characterized by production of IL-17, that differentiate in response to TGF and IL-6 and participate in the pathogenesis of several autoimmune diseases. Using RT-PCR analysis of gene expression, we analyzed the presence of TH1 (IL-12 and IFN) and TH17 (TGF, IL-6, IL-17A, IL-17F and IL-23) related cytokines in intestinal biopsies from CD patients with active disease compared to remission and from treated patients after acute, in vitro re-exposure to gliadin. Potent TH1 and TH17 responses were present in the active stage of the disease, whereas short incubation of normalized biopsies with gliadin did not increase the expression of the effector cytokines, although a tendency of upregulation for both TH1 and TH17 promoting factors was observed, suggestive of a reactivation of proinflammatory pathways. These results place CD into the group of autoimmune disorders in which TH17 cells also participate, although the relative importance of each T cell response and their role in the initial events of the disease need further investigation.
引用
收藏
页码:69 / 73
页数:5
相关论文
共 13 条
[1]   Th17 cell induction and immune regulatory effects [J].
Bi, Yujing ;
Liu, Guangwei ;
Yang, Ruifu .
JOURNAL OF CELLULAR PHYSIOLOGY, 2007, 211 (02) :273-278
[2]  
Blauvelt A., 2007, Expert Rev. Dermatol, V2, P69, DOI DOI 10.1586/17469872.2.1.69
[3]  
Cooke Anne, 2006, Review of Diabetic Studies, V3, P72, DOI 10.1900/RDS.2006.3.72
[4]   FiRe and microarrays:: a fast answer to burning questions [J].
Garcion, Christophe ;
Metraux, Jean-Pierre .
TRENDS IN PLANT SCIENCE, 2006, 11 (07) :320-322
[5]   Expanding the effector CD4 T-cell repertoire: the Th17 lineage [J].
Harrington, Laurie E. ;
Mangan, Paul R. ;
Weaver, Casey T. .
CURRENT OPINION IN IMMUNOLOGY, 2006, 18 (03) :349-356
[6]   The IL-23/IL-17 axis in inflammation [J].
Iwakura, Y ;
Ishigame, H .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (05) :1218-1222
[7]   Either a Th17 or a Th1 effector response can drive autoimmunity: conditions of disease induction affect dominant effector category [J].
Luger, Dror ;
Silver, Phyllis B. ;
Tang, Jun ;
Cua, Daniel ;
Chen, Zoe ;
Iwakura, Yoichiro ;
Bowman, Edward P. ;
Sgambellone, Nicole M. ;
Chan, Chi-Chao ;
Caspi, Rachel R. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2008, 205 (04) :799-810
[8]   MICA response to gliadin in intestinal mucosa from celiac patients [J].
Martín-Pagola, A ;
Pérez-Nanclares, G ;
Ortiz, L ;
Vitoria, J ;
Hualde, I ;
Zaballa, R ;
Preciado, E ;
Castaño, L ;
Bilbao, JR .
IMMUNOGENETICS, 2004, 56 (08) :549-554
[9]   Analysis of the expression of MICA in small intestinal mucosa of patients with celiac disease [J].
Martín-Pagola, A ;
Ortiz, L ;
De Nanclares, GP ;
Vitoria, JC ;
Castaño, L ;
Bilbao, JR .
JOURNAL OF CLINICAL IMMUNOLOGY, 2003, 23 (06) :498-503
[10]  
Montale E, 2001, AKZENTE-Z LIT, V48, P429