期刊文献+

主要组织相容性复合物Ⅰ类抗原在特发性炎性肌病中的表达研究

Study of expression of major histocompability complex Ⅰ antigen in idiopathic inflammatory myopathies
下载PDF
导出
摘要 目的探讨主要组织相容性复合物Ⅰ类抗原(MHC-Ⅰ)在特发性炎性肌病(IIM)中的表达及其意义。方法对15例IIM患者(IIM组,多发性肌炎14例、皮肌炎1例)、23例其他肌病患者(OM组,肢带型肌营养不良18例、脂质沉积性肌病4例、糖原累积性肌病1例)及5例无肌病对照者(NC组)的骨骼肌标本进行MHC-Ⅰ免疫组化染色。结果NC组未见MHC-Ⅰ表达;IIM组肌纤维MHC-Ⅰ阳性率为86.7%(13/15),明显高于OM组(26.1%,6/23)(P<0.005)。IIM组MHC-Ⅰ阳性表达的敏感性为86.7%,95%CI:59%~98%;特异性为73.9%,95%CI:55%~91%。结论 IIM患者肌纤维MHC-Ⅰ阳性表达高。MHC-Ⅰ免疫组化染色是一种较好的辅助IIM病理诊断的方法。 Objective To study the expression and its meaning of major histocompability complex Ⅰ (MHC- Ⅰ) antigen in idiopathic inflammatory myopathy (IIM) . Methods The MHC-Ⅰ antigen was detected by immunohistochemistry in muscle samples of 15 patients with IIM (IIM group,including 14 cases of polymyositis and 1 case of dermatomyositis) ,23 patients with other myopathies (OM group,including 18 cases of limb-girdle muscular dystrophy,4 cases of lipid storage myopathy and 1 case of glycogen storage myopathy) and 5 normal controls without myopathy (NC group) . Results There was no expression of MHC-Ⅰ in NC group. The positive rate of MHC-Ⅰ antigen was 86. 7% (13 /15) in IIM group,which was significantly higher than in OM group (26. 1% ,6 /23) (P 0. 005) . The sensitivity of MHC-Ⅰ in IIM group was 86. 7% ,95% CI: 59% - 98% ; and the specificity of MHC-Ⅰ in IIM group was 73. 9% ,95% CI: 55% - 91% . Conclusions The positive expression of MHC-Ⅰ is high in IIM patients. The immunohistological chemistry staining of MHC-Ⅰ can be a good pathological diagnostic method for IIM.
出处 《临床神经病学杂志》 CAS 北大核心 2010年第5期329-331,共3页 Journal of Clinical Neurology
基金 江西省卫生厅计划课题(20071055)
关键词 特发性炎性肌病 主要组织相容性复合物Ⅰ类抗原 idiopathic inflammatory myopathy major histocompability complex Ⅰ antigen
  • 相关文献

参考文献11

  • 1Dalakas MC, Hohlfeld R. Polymyositis and dermatomyositis [ J]. Lancet, 2003, 362: 971.
  • 2Dalakas MC. Inflammatory disorders of muscle:progress in polymyositis, dermatomyositis and inclusion body myositis [J]. Curr Opin Neurol,2004,17:561.
  • 3焉传祝.特发性炎性肌病的免疫病理及诊断[J].中华神经科杂志,2006,39(4):217-219. 被引量:5
  • 4Appleyard ST,Dunn MJ,Dubowitz V, et al. Increases expression of HLA ABC class I antigens by muscle fibres in Duchenne muscular dystrophy, inflammatory myopathy, and other neuromuscular disorders[J]. Lancet, 1985,8: 361.
  • 5Karpati G, Pouliot Y, Carpenter S. Expression of immunoreactive major histocompatibility complex products in human skeletal muscles [ J ]. Ann Neurol, 1998,23 : 64.
  • 6MeDouall RM, Dunn MJ, Dubowitz V. Expression of class I and class II MHC antigens in neuromuscular diseases[ J ]. J Neurol Sci, 1989,89:213.
  • 7Bohan A,Peter JB. Polymyositis and dermatomyositis[ J ]. N Engl J Med, 1975, 292: 344.
  • 8van der Pas J, Hengstman GJ, Ter Laak HJ, et al. Diagnostic value of MHC class I staining in idiopathic inflammatory myopathies[ J ]. J Neurol Neurosurg Psychiatry,2004,75:136.
  • 9韩顺昌,蒲传强,郎森阳,吴卫平,黄旭升.主要组织相容性抗原-Ⅰ表达在多发性肌炎诊断中的作用[J].中华医学杂志,2007,87(11):754-756. 被引量:2
  • 10郭华,李娜,袁栋才,朱建国,魏琰,胡静.肢带型肌营养不良2B型的临床和病理特点[J].临床神经病学杂志,2008,21(5):321-323. 被引量:2

二级参考文献37

  • 1李志军,唐荣华,胡晓晴,唐娜.脂质沉积性肌病的临床、神经电生理和病理学特征[J].临床神经病学杂志,2006,19(6):450-452. 被引量:12
  • 2笪宇威,贾建平,李彦,王敏.原发性肉碱缺乏致脂质沉积性肌病的临床与病理特点[J].临床神经病学杂志,2007,20(3):191-193. 被引量:6
  • 3Bruno C, DiMauro S. Lipid storage myopathies [ J ]. Curr Opin Neurol, 2008, 21 : 601.
  • 4Bradley WG, Hudgson P, Gardner-Medwin D, et al. Myopathy associated with abnormal lipid metabolism in skeletal muscle [ J]. Lancet, 1969, 1:495.
  • 5Engel AG, Angelini C. Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: a new syndrome [J]. Science, 1973, 179:899.
  • 6Kaplan JC. Gene table of monogenic neuromuscular disorders ( nuclear genome only) [J]. Neuromuscul Disord, 2009, 19: 77.
  • 7Uppin MS, Sundaram C, Meena AK, et al. Lipid storage myopathies with unusual clinical manifestations [ J ]. Neurology India, 2008, 56: 391.
  • 8Bruno C, Bertini E, Di Rocco M, et al. Clinical and genetic characterization of Chanarin-Dorfman syndrome [ J ]. Biochem Biophys Res Commun, 2008, 369: 1125.
  • 9Amat di San Filippo C,Taylor MR, Mestroni L, et al. Cardiomyopathy and carnitine deficiency [ J]. Mol Genet Metab,2008,94:162.
  • 10Gosalakkal JA, Kamoji V. Reye syndrome and Reyelike syndrome [ J]. Pediatr Neurol, 2008, 39 : 198.

共引文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部