Sjöström H, Lundin K E, Molberg O, Körner R, McAdam S N, Anthonsen D, Quarsten H, Norén O, Roepstorff P, Thorsby E, Sollid L M
Department of Medical Biochemistry and Genetics, The Panum Institute, University of Copenhagen, Denmark.
Scand J Immunol. 1998 Aug;48(2):111-5. doi: 10.1046/j.1365-3083.1998.00397.x.
Coeliac disease probably results from a T-cell response to wheat gliadin and is associated to HLA-DQ2. No gliadin epitopes recognized by intestinal T cells have yet been identified, limiting our understanding of the pathogenesis. Gut-lesion-derived DQ2-restricted T cells from coeliac disease patients were used to identify an epitope within a purified gamma-type gliadin. The structure of the epitope was characterized by mass spectrometry and verified by synthesis. The epitope (QPQQSFPEQQ) results from deamidation of a distinct glutamine in the native structure. This deamidation is important for binding to DQ2 and T-cell recognition. Other gut-derived T cells fail to recognize the epitope, although deamidation of unfractionated gliadin enhances the response of all gut-derived DQ2-restricted T cells isolated from several patients. Several DQ2-restricted T-cell epitopes exist, but for all of them deamidation of glutamine residues appears to be critical for creation of active epitopes. Native gliadin has few negatively charged residues but is very rich in glutamine. After deamidation gliadin becomes a rich source of DQ2 epitopes thus providing a link between DQ2, gliadin and coeliac disease. The necessity for modification may have general immunological relevance.
乳糜泻可能是由T细胞对小麦醇溶蛋白的反应引起的,并且与HLA - DQ2相关。目前尚未鉴定出肠道T细胞识别的醇溶蛋白表位,这限制了我们对发病机制的理解。来自乳糜泻患者的肠道病变来源的DQ2限制性T细胞被用于鉴定纯化的γ型醇溶蛋白中的一个表位。通过质谱对该表位的结构进行了表征,并通过合成进行了验证。该表位(QPQQSFPEQQ)是由天然结构中一个独特的谷氨酰胺脱酰胺化产生的。这种脱酰胺化对于与DQ2结合和T细胞识别很重要。其他肠道来源的T细胞无法识别该表位,尽管未分级的醇溶蛋白脱酰胺化增强了从几名患者中分离出的所有肠道来源的DQ2限制性T细胞的反应。存在几种DQ2限制性T细胞表位,但对于所有这些表位,谷氨酰胺残基的脱酰胺化似乎对于活性表位的产生至关重要。天然醇溶蛋白带负电荷的残基很少,但谷氨酰胺非常丰富。脱酰胺化后,醇溶蛋白成为DQ2表位的丰富来源,从而在DQ2、醇溶蛋白和乳糜泻之间建立了联系。这种修饰的必要性可能具有普遍的免疫学意义。