Publication | Closed Access
Human Leukocyte Antigen DQ2.2 and Celiac Disease
48
Citations
18
References
2012
Year
HlaHistocompatibilityImmunodeficienciesImmunologyGenetic EpidemiologyGastroenterologyPathologyClinical PresentationCeliac DiseaseImportant Hla-typeHematologyAutoimmune DiseaseHuman Leukocyte AntigenAutoimmunityImmunologic DiseaseInborn Error Of ImmunityPediatricsHla TypingMedicine
Patients with celiac disease (CD) lacking both human leukocyte antigen (HLA)-DQ2.5 in cis (DQA1*05:01, DQB1*02:01) or trans (DQA1*05:05, DQB1*02:02) configuration and HLA-DQ8 (DQA1*03:01, DQB1*03:02) are considered to be rare. Therefore, absence of these genotypes is commonly used to exclude the diagnosis of CD. To investigate whether this approach is justified, the HLA-distribution in 155 children with CD was studied. A total of 139 (89.7%) patients carried HLA-DQ2.5. Of the remaining patients, 7 (4.5%) carried HLA-DQ8. Interestingly, the 9 (5.8%) patients lacking HLA-DQ2.5 and HLA-DQ8 carried HLA-DQA1*02:01 and -DQB1*02:02 (HLA-DQ2.2). Therefore, HLA-DQ2.2 should be included as an important HLA-type related to CD.
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