The Role of Human Leukocyte Antigen in Celiac Disease Diagnostics

被引:13
作者
Lazar-Molnar, Eszter [1 ]
Snyder, Melissa [2 ]
机构
[1] Univ Utah, Sch Med, Dept Pathol, ARUP Labs, 500 Chipeta Way,MS 115, Salt Lake City, UT 84108 USA
[2] Mayo Clin, Dept Lab Med & Pathol, 200 First St Southwest, Rochester, MN 55905 USA
关键词
Celiac disease; HLA-DQ2; HLA-DQ8; Disease association; EUROPEAN GENETICS CLUSTER; GENOME-WIDE ASSOCIATION; TISSUE TRANSGLUTAMINASE; UNITED-STATES; T-CELLS; AT-RISK; ANTIBODY; GLUTEN; IDENTIFICATION; PREVALENCE;
D O I
10.1016/j.cll.2018.07.007
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 is an autoimmune disease affecting the small intestine, triggered by gluten sensitization in genetically susceptible individuals worldwide. Celiac disease development is strongly linked to the presence of HLA-DQ2 and/or DQ8, which present the immunogenic gluten peptides and trigger the immune response leading to pathogenesis. Because of the variability of clinical symptoms, the disease is often underdiagnosed. Intestinal biopsy and the presence of antibodies to deamidated gliadin and tissue transglutaminase are recommended diagnostic tools. Genetic testing for HLA DQ2 and DQ8 can be used to rule out disease in at-risk populations.
引用
收藏
页码:655 / 668
页数:14
相关论文
共 42 条
[1]   Integration of Genetic and Immunological Insights into a Model of Celiac Disease Pathogenesis [J].
Abadie, Valerie ;
Sollid, Ludvig M. ;
Barreiro, Luis B. ;
Jabri, Bana .
ANNUAL REVIEW OF IMMUNOLOGY, VOL 29, 2011, 29 :493-525
[2]  
Aleanzi M, 2001, CLIN CHEM, V47, P2023
[3]   Antibody responses to deamidated gliadin peptide show high specificity and parallel antibodies to tissue transglutaminase in developing coeliac disease [J].
Ankelo, M. ;
Kleimola, V. ;
Simell, S. ;
Simell, O. ;
Knip, M. ;
Jokisalo, E. ;
Tarkia, M. ;
Westerlund, A. ;
He, Q. ;
Viander, M. ;
Ilonen, J. ;
Hinkkanen, A. E. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2007, 150 (02) :285-293
[4]  
[Anonymous], 2016, WORLD GASTR ORG GLOB
[5]  
Bevan S, 1999, J MED GENET, V36, P687
[6]   T-Cell Response to Gluten in Patients With HLA-DQ2.2 Reveals Requirement of Peptide-MHC Stability in Celiac Disease [J].
Bodd, Michael ;
Kim, Chu-Young ;
Lundin, Knut E. A. ;
Sollid, Ludvig M. .
GASTROENTEROLOGY, 2012, 142 (03) :552-561
[7]   IGA ANTI-ENDOMYSIUM ANTIBODY - A NEW IMMUNOLOGICAL MARKER OF DERMATITIS-HERPETIFORMIS AND CELIAC-DISEASE [J].
CHORZELSKI, TP ;
BEUTNER, EH ;
SULEJ, J ;
TCHORZEWSKA, H ;
JABLONSKA, S ;
KUMAR, V ;
KAPUSCINSKA, A .
BRITISH JOURNAL OF DERMATOLOGY, 1984, 111 (04) :395-402
[8]   Genetics of Type 1A Diabetes [J].
Concannon, Patrick ;
Rich, Stephen S. ;
Nepom, Gerald T. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (16) :1646-1654
[9]   Coeliac disease [J].
Di Sabatino, Antonio ;
Corazza, Gino Roberto .
LANCET, 2009, 373 (9673) :1480-1493
[10]   Identification of tissue transglutaminase as the autoantigen of celiac disease [J].
Dieterich, W ;
Ehnis, T ;
Bauer, M ;
Donner, P ;
Volta, U ;
Riecken, EO ;
Schuppan, D .
NATURE MEDICINE, 1997, 3 (07) :797-801