自身免疫性胰腺炎:是自身免疫性疾病还是免疫炎性疾病?

Yvonne Hsieh, Sudhanshu Agrawal, Leman Yel, Sudhir Gupta
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摘要

自身免疫性胰腺炎(AIP)被广泛认为是一种自身免疫性疾病,其特征是IgG和/或IgG4升高,自身抗体的存在,淋巴细胞和浆细胞浸润伴纤维化。然而,尚未发表详细的免疫学研究。详细定义AIP的免疫学变化,并回顾自身免疫的证据,这些证据可能是抗原特异性的,可能在AIP的发病机制中起作用,从而确定AIP是否为自身免疫性疾病。在一例AIP患者中进行了先天性和适应性免疫反应的详细免疫学调查。文献综述从Pub med和Medline检索中进行。AIP患者的免疫学分析显示,促炎IL-6和IL-17的产生增加,NK细胞活性增加。未检测到器官特异性或非特异性抗体。血清IgG4与疾病活动性或对类固醇治疗的反应之间没有相关性。文献回顾显示AIP缺乏自身抗原特异性T细胞和B细胞反应,自身抗体仅在一部分患者中存在,并且对胰腺组织抗原不具有特异性。因此,我们建议将其称为免疫炎性胰腺炎,而不是自身免疫性胰腺炎。自身免疫性胰腺炎的典型特征是成像显示主胰管弥漫性或节段性狭窄,IgG和/或IgG4升高,自身抗体存在,淋巴细胞和浆细胞浸润,纤维化存在。已检测的自身抗体包括ANA、抗微粒体抗体、抗甲状腺球蛋白抗体、抗胰腺分泌胰蛋白酶抑制剂、乳铁蛋白和碳氨水解酶的抗体(2-5)。然而,这些自身抗体的存在仅在有限数量的病例中零星记录。此外,这些自身抗体中有许多是直接针对同样存在于唾液腺、胆管和远端肾小管中的抗原的。IgG、IgG4、抗核抗体、类风湿因子的检测
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Autoimmune Pancreatitis: An Autoimmune or Immunoinflammatory Disease?
Autoimmune pancreatitis (AIP) has been widely presumed to be an autoimmune disease that is characterized by elevated IgG and/or IgG4, the presence of autoantibodies, and an infiltration of lymphocytes and plasma cells with fi- brosis. However, no detailed immunological studies have been published. To define immunological changes in AIP in de- tail, and to review evidence for autoimmunity which may be antigen specific and may play a role in the pathogenesis of AIP, and therefore, to determine whether AIP is an autoimmune disease. A detailed immunological investigation for both innate and adaptive immune responses was performed in a patient with AIP. Review of literature was performed from Pub med, and Medline search. Immunological analysis of patient with AIP revealed increased production of proinflammatory IL-6, and IL-17, and increased NK cell activity. No organ-specific or non-specific antibodies were detected. There was no correlation between serum IgG4 with disease activity or response to steroid therapy. Review of literature revealed lack of auto-antigen-specific T and B cell responses in AIP, and autoantibodies are present only in a subset of patients, and are not specific to pancreatic tissue antigens. Therefore, we propose the term Immunoinflammatory pancreatitis rather than an autoimmune pancreatitis. Autoimmune pancreatitis is typically characterized by a diffuse or segmental narrowing of the main pancreatic duct on imaging, elevated IgG and/or IgG4, the presence of autoantibodies, an infiltration of lymphocytes and plasma cells, and presence of fibrosis. The autoantibodies that have been examined include ANA, anti-microsomal antibodies, anti-thyroglobulin antibodies, and antibodies against pancre- atic secretory trypsin inhibitor, lactoferrin, and carbonic an- hydrase (2-5). However, the presence of these autoantibodies has been only sporadically documented in limited numbers of cases. In addition, many of these autoantibodies are di- rected against antigens that are also present in the salivary gland, biliary duct, and distal renal tubules. The detection of IgG, IgG4, antinuclear antibodies, and rheumatoid factor
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