Guillevin L, Ronco P, Verroust P
Hôpital Avicenne, Department of Internal Medicine, Bobigny, France.
J Autoimmun. 1990 Dec;3(6):789-92. doi: 10.1016/s0896-8411(05)80044-7.
Levels of immune complexes (IC) were measured before treatment in 16 patients affected with classic polyarteritis nodosa (PN) or Churg Strauss Angiitis (CSA). The six patients with PN were positive for HBV markers. The others presented severe asthma. IgG containing immune complexes were measured using Raji cell assay. Normal level was 4,642 +/- 509 (mean +/- SEM). IC levels were significantly different in patients with and without HBV markers. When HBV was present, mean IC level was 7,185 +/- 2,472. In the absence of HBV markers, mean IC level was 26,462 +/- 10,796. These results confirm that systemic vasculitis is an heterogeneous group of diseases and further suggest that pathogenesis of vasculitis is different in patients with asthma and those with HBV markers.
在16例患有经典结节性多动脉炎(PN)或变应性肉芽肿性血管炎(CSA)的患者治疗前检测免疫复合物(IC)水平。6例PN患者乙肝标志物呈阳性。其他患者有严重哮喘。使用Raji细胞试验检测含IgG的免疫复合物。正常水平为4,642±509(平均值±标准误)。有和没有乙肝标志物的患者IC水平有显著差异。当存在乙肝病毒时,平均IC水平为7,185±2,472。在没有乙肝标志物时,平均IC水平为26,462±10,796。这些结果证实系统性血管炎是一组异质性疾病,并进一步表明哮喘患者和有乙肝标志物患者的血管炎发病机制不同。