Future therapeutic options for celiac disease

被引:118
作者
Sollid, LM [1 ]
Khosla, C
机构
[1] Univ Oslo, Rikshop Univ Hosp, Inst Immunol, N-0027 Oslo, Norway
[2] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Biochem, Stanford, CA 94305 USA
来源
NATURE CLINICAL PRACTICE GASTROENTEROLOGY & HEPATOLOGY | 2005年 / 2卷 / 03期
关键词
celiac disease; gluten; T cells; therapy; tissue transglutaminase;
D O I
10.1038/ncpgasthep0111
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Celiac disease is a disorder of the small intestine caused by an inappropriate immune response to wheat gluten and similar proteins of barley and rye. At present, the only available treatment is a strict gluten-exclusion diet; hence the need for alternative treatments. Recent advances have improved our understanding of the molecular basis for this disorder and there are several attractive targets for new treatments. Oral enzyme supplementation is designed to accelerate gastrointestinal degradation of proline-rich gluten, especially its proteolytically stable antigenic peptides. Complementary strategies aiming to interfere with activation of gluten-reactive T cells include the inhibition of intestinal tissue transglutaminase activity to prevent selective deamidation of gluten peptides, and blocking the binding of gluten peptides to the HLA-DQ2 or HLA-DQ8 molecules. Other possible treatments include cytokine therapy, and selective adhesion molecule inhibitors that interfere with inflammatory reactions, some of which are already showing promise in the clinic for other gastrointestinal diseases.
引用
收藏
页码:140 / 147
页数:8
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