期刊
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
卷 20, 期 14, 页码 -出版社
MDPI
DOI: 10.3390/ijms20143400
关键词
mast cells; coeliac disease; gliadin immunology; p31-43 fragment; 33-mer peptide; 25-mer fragment
资金
- Tuscany section of the Associazione Italiana Celiachia
Over the last decades, there has been an impressive progress in our understanding of coeliac disease pathogenesis and it has become clear that the disorder is the final result of complex interactions of environmental, genetic, and immunological factors. Coeliac disease is now considered a prototype of T-cell-mediated disease characterized by loss of tolerance to dietary gluten and the targeted killing of enterocytes by T-cell receptor alpha beta intraepithelial lymphocytes. Accumulating evidence, however, indicates that the induction of a gluten-specific T helper-1 response must be preceded by the activation of the innate immune system. Mast cells are key players of the innate immune response and contribute to the pathogenesis of a multitude of diseases. Here, we review the results of studies aimed at investigating the role of mast cells in the pathogenesis of coeliac disease, showing that these cells increase in number during the progression of the disease and contribute to define a pro-inflammatory microenvironment.
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