| Literature DB >> 22535446 |
Shuo-Wang Qiao1, Rasmus Iversen, Melinda Ráki, Ludvig M Sollid.
Abstract
Compared to other human leukocyte antigen (HLA)-associated diseases such as type 1 diabetes, multiple sclerosis, and rheumatoid arthritis, fundamental aspects of the pathogenesis in celiac disease are relatively well understood. This is mostly because the causative antigen in celiac disease-cereal gluten proteins-is known and the culprit HLA molecules are well defined. This has facilitated the dissection of the disease-relevant CD4+ T cells interacting with the disease-associated HLA molecules. In addition, celiac disease has distinct antibody responses to gluten and the autoantigen transglutaminase 2, which give strong handles to understand all sides of the adaptive immune response leading to disease. Here we review recent developments in the understanding of the role of T cells, B cells, and antigen-presenting cells in the pathogenic immune response of this instructive disorder.Entities:
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Year: 2012 PMID: 22535446 DOI: 10.1007/s00281-012-0314-z
Source DB: PubMed Journal: Semin Immunopathol ISSN: 1863-2297 Impact factor: 9.623