Korponay-Szabó Ilma R
J Pediatr Gastroenterol Nutr. 2014 Jul;59 Suppl 1:S11-3. doi: 10.1097/01.mpg.0000450395.68897.c1.
Celiac disease (CD) is triggered by the consumption of gluten-containing cereals to which patients mount a T-lymphocyte and antibody response in both immunoglobulin A and immunoglobulin G classes coupled with autoantibody production against self-proteins, predominantly type-2 (tissue) transglutaminase (TG2). TG2 autoantibodies are biologically active and bind to their target protein in the patients' tissues, including the gut and extraintestinal tissues. This peculiar systemic anti-TG2 reaction is dependent on the presence of dietary gluten and stops after its elimination. As both anti-TG2 and anti-gliadin antibodies are activity markers, their detection is valuable for the disease recognition and therapy monitoring. High concentrations of serum anti-TG2 antibody positivity supported by highly specific positivity for endomysial antibodies became the critical component of celiac disease diagnosis, although serum antibodies as indirect markers have limitations and are not able to replace histology analysis in all cases. Studies focusing on tissue-bound antibodies may further improve our understanding of their role.
乳糜泻(CD)由摄入含麸质谷物引发,患者会对其产生T淋巴细胞反应以及免疫球蛋白A和免疫球蛋白G类抗体反应,并产生针对自身蛋白的自身抗体,主要是2型(组织)转谷氨酰胺酶(TG2)。TG2自身抗体具有生物活性,可在患者组织(包括肠道和肠外组织)中与其靶蛋白结合。这种特殊的全身性抗TG2反应取决于饮食中麸质的存在,在麸质消除后停止。由于抗TG2和抗麦醇溶蛋白抗体都是活性标志物,它们的检测对于疾病识别和治疗监测具有重要价值。高浓度血清抗TG2抗体阳性以及肌内膜抗体高度特异性阳性是乳糜泻诊断的关键组成部分,尽管血清抗体作为间接标志物存在局限性,且在所有情况下都无法替代组织学分析。专注于组织结合抗体的研究可能会进一步增进我们对其作用的理解。