仅在伴有乳糜泻合并症的1型糖尿病患者的肠道黏膜中,t细胞介导的麦胶蛋白免疫被激发

IF 6.2 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Diabetes Pub Date : 2025-06-24 DOI:10.2337/db24-1120
Carmen Gianfrani, Alessandra Camarca, Stefania Picascia, Serena Vitale, Ilaria Mottola, Martina Carpinelli, Mariantonia Maglio, Silvia Gregori, Adriana Franzese, Renata Auricchio, Riccardo Troncone
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引用次数: 0

摘要

1型糖尿病(T1D)和乳糜泻(CeD)是两种高度相关的自身免疫性疾病,因为它们具有相同的遗传危险因素和免疫致病机制。一些研究表明,谷蛋白,CeD的致病抗原,在T1D发病机制的含义。我们研究了是否在T1D患儿的肠道黏膜中存在麦胶蛋白特异性t细胞反应性,无论是否合并CeD。纳入33名幼儿(中位年龄10岁),并根据T1D和/或CeD诊断分为五组。所有患者均行上内镜检查,怀疑有CeD或胃肠道不适,并处理十二指肠活检标本,分析淋巴样细胞表型和T细胞介导的对麦胶蛋白的反应。各组之间各种t细胞亚群的百分比没有发现实质性差异。在CeD阴性的T1D儿童中没有发现麦胶蛋白t细胞反应性,也存在中和调节细胞因子白介素10和转化生长因子β的抗体。相比之下,在潜在(CeD相关自身抗体阳性和正常粘膜组织学)或完全CeD(绒毛萎缩)的T1D中检测到对麦胶蛋白的显著t细胞反应。综上所述,在没有CeD合并症的T1D儿童的小肠中没有对谷蛋白的适应性免疫。人们一直假设饮食蛋白质在1型糖尿病的发病过程中起着环境因素的作用。本研究调查了有无乳糜泻合并症的1型糖尿病儿童小肠中是否存在麦胶蛋白特异性T细胞。乳糜泻自身免疫阴性的1型糖尿病儿童的肠道粘膜中未观察到麦胶蛋白反应性T细胞的迹象,无论是促炎细胞还是调节性T细胞。在抗组织转谷氨酰胺酶抗体血清阳性的糖尿病患儿肠黏膜活检标本中检测到产生干扰素γ的T细胞。我们的研究不支持肠道T细胞介导的谷蛋白免疫在1型糖尿病发病中的致病作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
T-Cell Mediated Immunity to Gliadin Is Elicited in the Gut Mucosa of Type 1 Diabetes Patients Only in Presence of Celiac Disease Comorbidity
Type 1 diabetes (T1D) and celiac disease (CeD) are two strongly associated autoimmune disorders, as they share genetic risk factors and immunopathogenic mechanisms. Several studies suggest an implication of gluten proteins, the causative antigen of CeD, in T1D pathogenesis. We investigated whether a gliadin-specific T-cell reactivity is present in the gut mucosa of children with T1D, with or without CeD comorbidity. Thirty-three young children were enrolled (median age 10 years) and divided in five groups based on T1D and/or CeD diagnosis. All patients underwent upper endoscopy for suspicion of CeD or gastrointestinal complaints, and duodenal biopsy specimens were processed for analysis of lymphoid cells phenotype and T cell–mediated reactiveness to gliadin. No substantial differences were found in the percentages of various T-cell subsets between the groups. No gliadin T-cell reactivity was found in T1D children negative for CeD, also in the presence of antibodies neutralizing regulatory cytokines interleukin 10 and transforming growth factor β. By contrast, a marked T-cell response to gliadin was detected in T1D with either potential (positive for CeD-associated autoantibodies and normal mucosa histology) or full-blown CeD (villous atrophy). In conclusion, no adaptive immunity to gluten occurs in the small intestine of T1D children in the absence of CeD comorbidity. Article Highlights It has been hypothesized that dietary proteins act as environmental factors in type 1 diabetes pathogenesis. This study investigated whether gliadin-specific T cells are present in the small intestine of children with type 1 diabetes, without or with celiac disease comorbidity. No sign of gliadin-reactive T cells, either proinflammatory or regulatory, was observed in the gut mucosa of children with type 1 diabetes negative for celiac disease autoimmunity. Interferon-γ producing T cells were detected in gut mucosa biopsy specimens of children with diabetes seropositive for antitissue transglutaminase antibodies. Our study does not support a pathogenic role of intestinal T cell–mediated immunity to gluten in type 1 diabetes pathogenesis.
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来源期刊
Diabetes
Diabetes 医学-内分泌学与代谢
CiteScore
12.50
自引率
2.60%
发文量
1968
审稿时长
1 months
期刊介绍: Diabetes is a scientific journal that publishes original research exploring the physiological and pathophysiological aspects of diabetes mellitus. We encourage submissions of manuscripts pertaining to laboratory, animal, or human research, covering a wide range of topics. Our primary focus is on investigative reports investigating various aspects such as the development and progression of diabetes, along with its associated complications. We also welcome studies delving into normal and pathological pancreatic islet function and intermediary metabolism, as well as exploring the mechanisms of drug and hormone action from a pharmacological perspective. Additionally, we encourage submissions that delve into the biochemical and molecular aspects of both normal and abnormal biological processes. However, it is important to note that we do not publish studies relating to diabetes education or the application of accepted therapeutic and diagnostic approaches to patients with diabetes mellitus. Our aim is to provide a platform for research that contributes to advancing our understanding of the underlying mechanisms and processes of diabetes.
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