Pathophysiology and immunogenetics of celiac disease

被引:20
作者
Aboulaghras, Sara [1 ,3 ]
Piancatelli, Daniela [2 ]
Oumhani, Khadija [3 ]
Balahbib, Abdelaali [4 ]
Bouyahya, Abdelhakim [5 ]
Taghzouti, Khalid [1 ]
机构
[1] Mohammed V Univ Rabat, Fac Sci Genom Human Pathol Res, Genom Human Pathol Res, Physiol & Physiopathol Team, Rabat, Morocco
[2] Natl Res Council CNR, Inst Translat Pharmacol IFT, Laquila, Italy
[3] Inst Natl Hyg, Lab Immunol, Rabat, Morocco
[4] Mohammed V Univ Rabat, Fac Sci, Lab Zool & Gen Biol, Rabat, Morocco
[5] Mohammed V Univ Rabat, Fac Sci, Genom Ctr Human Pathol Res, Dept Biol,Lab Human Pathol Biol, Rabat, Morocco
关键词
Celiac disease; HLA; Physiopathology; Transglutaminase; 2; Microbiota; RESTRICTED T-CELLS; GLUTEN-FREE DIET; TISSUE TRANSGLUTAMINASE; HLA-DQ; INTERFERON-GAMMA; GUT MICROBIOTA; INTESTINAL PERMEABILITY; STORAGE PROTEINS; GLIADIN; PREVALENCE;
D O I
10.1016/j.cca.2022.01.022
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Celiac disease (CD) is a chronic inflammatory enteropathy caused by gluten (protein from wheat, rye and, barley) in genetically predisposed individuals carrying the HLA-DQ2/HLA-DQ8 genotype. This pathology has a multi factorial etiology in which HLA genes, the microbiome, gluten and, other environmental factors are involved in the development of the disease. Its pathogenesis involves both innate and adaptive immunity as well as upregulation of IL-15. The objective of this review is to examine the results of current studies on genetic and environmental variables to better understand the pathogenesis of this enteropathy. The complex etiology of celiac disease makes our understanding of the pathogenesis of the disease incomplete, and a better knowledge of the many genetic and environmental components would help us better understand the pathophysiology of celiac disease.
引用
收藏
页码:74 / 83
页数:10
相关论文
共 148 条
[91]   Gliadin specific, HLA DQ2-restricted T cells are commonly found in small intestinal biopsies from coeliac disease patients, but not from controls [J].
Molberg, O ;
Kett, K ;
Scott, H ;
Thorsby, E ;
Sollid, LM ;
Lundin, KEA .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1997, 46 (01) :103-108
[92]   Regulation of the T helper cell type 1 transcription factor T-bet in coeliac disease mucosa [J].
Monteleone, I ;
Monteleone, G ;
Blanco, GD ;
Vavassori, P ;
Cucchiara, S ;
MacDonald, TT ;
Pallone, F .
GUT, 2004, 53 (08) :1090-1095
[93]   Characterization of IL-17A-Producing Cells in Celiac Disease Mucosa [J].
Monteleone, Ivan ;
Sarra, Massimiliano ;
Blanco, Giovanna Del Vecchio ;
Paoluzi, Omero Alessandro ;
Franze, Eleonora ;
Fina, Daniele ;
Fabrizi, Alessia ;
MacDonald, Thomas T. ;
Pallone, Francesco ;
Monteleone, Giovanni .
JOURNAL OF IMMUNOLOGY, 2010, 184 (04) :2211-2218
[94]   HLA-DQ2 and-DQ8 genotype frequency Syrian celiac disease children: HLA-DQ relative risks evaluation [J].
Murad, Hossam ;
Jazairi, Batoul ;
Khansaa, Issam ;
Olabi, Doaa ;
Khouri, Lina .
BMC GASTROENTEROLOGY, 2018, 18
[95]  
Murphy K., 2016, Janeway's Immunobiology
[96]   The prevalence of celiac disease in Europe: Results of a centralized, international mass screening project [J].
Mustalahti, Kirsi ;
Catassi, Carlo ;
Reunanen, Antti ;
Fabiani, Elisabetta ;
Heier, Margit ;
McMillan, Stan ;
Murray, Liam ;
Metzger, Marie-Helene ;
Gasparin, Maurizio ;
Bravi, Enzo ;
Maki, Markku .
ANNALS OF MEDICINE, 2010, 42 (08) :587-595
[97]   P31-43, an undigested gliadin peptide, mimics and enhances the innate immune response to viruses and interferes with endocytic trafficking: a role in celiac disease [J].
Nanayakkara, Merlin ;
Lania, Giuliana ;
Maglio, Mariantonia ;
Auricchio, Renata ;
De Musis, Cristiana ;
Discepolo, Valentina ;
Miele, Erasmo ;
Jabri, Bana ;
Troncone, Riccardo ;
Auricchio, Salvatore ;
Barone, Maria Vittoria .
SCIENTIFIC REPORTS, 2018, 8
[98]   The role of Th1/Th2 polarization in mucosal immunity [J].
Neurath, MF ;
Finotto, S ;
Glimcher, LH .
NATURE MEDICINE, 2002, 8 (06) :567-573
[99]   Gluten induces an intestinal cytokine response strongly dominated by interferon gamma in patients with celiac disease [J].
Nilsen, EM ;
Jahnsen, FL ;
Lundin, KEA ;
Johansen, FE ;
Fausa, O ;
Sollid, LM ;
Jahnsen, J ;
Scott, H ;
Brandtzaeg, P .
GASTROENTEROLOGY, 1998, 115 (03) :551-563
[100]   GLUTEN SPECIFIC, HLA-DQ RESTRICTED T-CELLS FROM CELIAC MUCOSA PRODUCE CYTOKINES WITH THL OR THO PROFILE DOMINATED BY INTERFERON-GAMMA [J].
NILSEN, EM ;
LUNDIN, KEA ;
KRAJCI, P ;
SCOTT, H ;
SOLLID, LM ;
BRANDTZAEG, P .
GUT, 1995, 37 (06) :766-776