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Standardization of the experimental autoimmune myasthenia gravis (EAMG) model by immunization of rats with Torpedo californica acetylcholine receptors — Recommendations for methods and experimental designs

机译:通过用加州鱼雷乙酰胆碱受体免疫大鼠对实验性自身免疫性重症肌无力(EAMG)模型进行标准化-方法和实验设计的建议

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摘要

Myasthenia gravis (MG) with antibodies against the acetylcholine receptor (AChR) is characterized by a chronic, fatigable weakness of voluntary muscles. The production of autoantibodies involves the dysregulation of T cells which provide the environment for the development of autoreactive B cells. The symptoms are caused by destruction of the postsynaptic membrane and degradation of the AChR by IgG autoantibodies, predominantly of the G1 and G3 subclasses. Active immunization of animals with AChR from mammalian muscles, AChR from Torpedo or Electrophorus electric organs, and recombinant or synthetic AChR fragments generates a chronic model of MG, termed experimental autoimmune myasthenia gravis (EAMG). This model covers cellular mechanisms involved in the immune response against the AChR, e.g. antigen presentation, T cell-help and regulation, B cell selection and differentiation into plasma cells. Our aim is to define standard operation procedures and recommendations for the rat EAMG model using purified AChR from the Torpedo californica electric organ, in order to facilitate more rapid translation of preclinical proof of concept or efficacy studies into clinical trials and, ultimately, clinical practice.
机译:重症肌无力(MG)带有针对乙酰胆碱受体(AChR)的抗体,其特征在于自愿性肌肉的慢性,可察觉的虚弱。自身抗体的产生涉及T细胞的失调,这为自身反应性B细胞的发育提供了环境。症状是由IgG自身抗体(主要是G1和G3亚类)的突触后膜破坏和AChR降解引起的。用哺乳动物肌肉中的AChR,鱼雷或电泳电器官中的AChR以及重组或合成的AChR片段对动物进行主动免疫可产生MG的慢性模型,称为实验性自身免疫性重症肌无力(EAMG)。该模型涵盖了参与针对AChR的免疫反应的细胞机制,例如AChR。抗原呈递,T细胞帮助和调节,B细胞选择和分化为浆细胞。我们的目标是使用来自加州鱼雷电器官的纯净AChR定义大鼠EAMG模型的标准操作程序和建议,以促进将概念前或临床研究的临床前证据更快速地转化为临床试验,并最终转化为临床实践。

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