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麸质共济失调中针对脑和肠道转谷氨酰胺酶的自身抗体靶向作用

Autoantibody targeting of brain and intestinal transglutaminase in gluten ataxia.

作者信息

Hadjivassiliou M, Mäki M, Sanders D S, Williamson C A, Grünewald R A, Woodroofe N M, Korponay-Szabó I R

机构信息

Department of Neurology, Royal Hallamshire Hospital, Sheffield, UK.

出版信息

Neurology. 2006 Feb 14;66(3):373-7. doi: 10.1212/01.wnl.0000196480.55601.3a.

Abstract

OBJECTIVE

To investigate the presence of autoantibody deposition against type 2 tissue transglutaminase (TG2; a reliable marker of the whole spectrum of gluten sensitivity) in the jejunal tissue and brain of patients with gluten ataxia and in control subjects.

METHODS

The authors evaluated jejunal biopsy samples from nine patients with gluten ataxia and seven patients with other causes of ataxia for the presence of TG2-related immunoglobulin deposits using double-color immunofluorescence. Autopsy brain tissue from one patient with gluten ataxia and one neurologically intact brain were also studied.

RESULTS

IgA deposition on jejunal TG2 was found in the jejunal tissue of all patients with gluten ataxia and in none of the controls. The intestinal IgA deposition pattern was similar to that seen in patients with overt and latent celiac disease and in those with dermatitis herpetiformis. Widespread IgA deposition around vessels was found in the brain of the patient with gluten ataxia but not the control brain. The deposition was most pronounced in the cerebellum, pons, and medulla.

CONCLUSIONS

Anti-tissue transglutaminase IgA antibodies are present in the gut and brain of patients with gluten ataxia with or without an enteropathy in a similar fashion to patients with celiac disease, latent celiac disease, and dermatitis herpetiformis but not in ataxia control subjects. This finding strengthens the contention that gluten ataxia is immune mediated and belongs to the same spectrum of gluten sensitivity as celiac disease and dermatitis herpetiformis.

摘要

目的

研究麸质共济失调患者及对照者空肠组织和大脑中针对2型组织转谷氨酰胺酶(TG2;麸质敏感性全谱的可靠标志物)的自身抗体沉积情况。

方法

作者使用双色免疫荧光法评估了9例麸质共济失调患者和7例其他原因所致共济失调患者的空肠活检样本中与TG2相关的免疫球蛋白沉积情况。还研究了1例麸质共济失调患者的尸检脑组织和1例神经功能正常者的脑组织。

结果

在所有麸质共济失调患者的空肠组织中均发现空肠TG2上有IgA沉积,而对照组中均未发现。肠道IgA沉积模式与显性和隐性乳糜泻患者以及疱疹样皮炎患者所见相似。在麸质共济失调患者的大脑中发现血管周围广泛存在IgA沉积,而对照者大脑中未发现。沉积在小脑、脑桥和延髓最为明显。

结论

麸质共济失调患者无论有无肠病,其肠道和大脑中均存在抗组织转谷氨酰胺酶IgA抗体,其方式与乳糜泻、隐性乳糜泻和疱疹样皮炎患者相似,但共济失调对照者中未发现。这一发现强化了麸质共济失调是免疫介导的这一观点,且其与乳糜泻和疱疹样皮炎属于同一麸质敏感性谱系。

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