Endoscopy Center and Endoscopy Research Institute, Zhongshan Hospital, Fudan University, Shanghai, China.
Shanghai Medical College, Fudan University, Shanghai, China.
J Dig Dis. 2021 Mar;22(3):126-135. doi: 10.1111/1751-2980.12973.
There is accumulating evidence suggesting that an autoimmune component is involved in esophageal achalasia. An increase in immune cells, cytokines, chemokines, and autoimmune antibodies in serum and infiltration of immune cells in tissues support the view that immune-mediated inflammation is a crucial pathogenesis of inhibitory neuron degeneration in the lower esophageal sphincter. Infection of viruses such as the herpes virus family has been suspected of provoking the autoimmune reaction. Meanwhile, previous reports on immunogenetics have proposed that specific risk alleles on the human leukocyte antigen complex define the susceptible population to achalasia. In this study we reviewed current knowledge regarding the immune-related factors of achalasia, including immunology, viral infection and immunogenetic variations.
越来越多的证据表明,自身免疫成分参与了食管失弛缓症的发生。免疫细胞、细胞因子、趋化因子和自身抗体在血清中的增加,以及免疫细胞在组织中的浸润,支持了免疫介导的炎症是下食管括约肌抑制性神经元退行性变的关键发病机制的观点。病毒感染,如疱疹病毒家族,被怀疑引发了自身免疫反应。与此同时,先前关于免疫遗传学的报告提出,人类白细胞抗原复合体上的特定风险等位基因定义了对失弛缓症易感的人群。在这项研究中,我们回顾了目前关于失弛缓症的免疫相关因素的知识,包括免疫学、病毒感染和免疫遗传学的变异。