4.7 Article

Novel therapies for coeliac disease

期刊

JOURNAL OF INTERNAL MEDICINE
卷 269, 期 6, 页码 604-613

出版社

WILEY
DOI: 10.1111/j.1365-2796.2011.02376.x

关键词

coeliac disease; drug; gluten; human leucocyte antigen; T cell; therapy; transglutaminase

资金

  1. Research Council of Norway
  2. European Commission
  3. South-Eastern Norway Regional Health Authority
  4. Norwegian Foundation for Health and Rehabilitation Research
  5. Juvenile Diabetes Research Foundation
  6. National Institutes of Health [R01 DK 063158]

向作者/读者索取更多资源

Sollid LM, Khosla C. (Institute of Immunology, University of Oslo and Oslo University Hospital, Oslo, Norway; Departments of Chemistry,Chemical Engineering and Biochemistry, Stanford University, Stanford, CA, USA) Novel therapies for coeliac disease (Symposium). J Intern Med 2011; 269: 604-613. Coeliac disease is a widespread, lifelong disorder for which dietary control represents the only accepted form of therapy. There is an unmet need for nondietary therapies to treat this condition. Most ongoing and emerging drug-discovery programmes are based on the understanding that coeliac disease is caused by an inappropriate T-cell-mediated immune response to dietary gluten proteins. Recent genome-wide association studies lend further support to this pathogenic model. The central role of human leucocyte antigen genes has been validated, and a number of new risk loci have been identified, most of which are related to the biology of T cells and antigen-presenting cells. Here, we review the status of potential nondietary therapies under consideration for coeliac disease. We conclude that future development of novel therapies will be aided considerably by the identification of new, preferably noninvasive, surrogate markers for coeliac disease activity.

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