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皮肌炎和多发性肌炎的免疫发病机制 被引量:1

Immunopathogenesis of dermatomyositis and polymyositis
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摘要 皮肌炎和多发性肌炎(DM/PM)的发病机制尚未完全清楚。感染导致的分子模拟以及变性的自身抗原作为疾病的启动因子,导致遗传易感个体免疫细胞包括B细胞、T细胞、树突细胞、吞噬细胞等功能和分化异常以及体液免疫发生改变,从而引起细胞因子和化学分子不适当产生及炎症反应,导致骨骼肌肉损伤以及其他系统受累。该文按照免疫反应发生的过程,系统地对DM/PM免疫发病机制进行综述。
出处 《国际儿科学杂志》 2009年第6期649-651,共3页 International Journal of Pediatrics
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同被引文献15

  • 1谢瑶,卢昕,王国春.肌炎特异性抗体在多发性肌炎和皮肌炎中的意义[J].中华风湿病学杂志,2005,9(11):645-649. 被引量:11
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  • 9张红,周华,毛继芳,秦美华.多发性肌炎、皮肌炎患者的肌电图研究[J].中国临床实用医学,2009,3(6):41-42. 被引量:3
  • 10张欣,史旭华,张烜,崔全才,张奉春.原发性胆汁性肝硬化的临床与肝脏病理相关性研究[J].中华风湿病学杂志,2011,15(2):75-78. 被引量:7

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