Kus J, Bergin C, Miller R, Ongley R, Churg A, Enarson D
Chest. 1985 Jun;87(6):826-7. doi: 10.1378/chest.87.6.826.
We report a case of allergic granulomatosis and angiitis (Churg-Strauss syndrome) in which immunologic parameters, including lymphocyte subpopulations, were determined in the acute phase of the disease and during remission. Hyperimmunoglobulinemia E and immune complexes were present. A low proportion of suppressor/cytotoxic (T8+) lymphocytes and a high helper/suppressor ratio were seen throughout the course of the disease, although immunoglobulin levels and circulating immune complex levels decreased with therapy. We hypothesize that the deficiency of suppressor cells may play a role in the pathogenesis of this syndrome.
我们报告了一例变应性肉芽肿病和血管炎(Churg-Strauss综合征),在此病例中,对疾病急性期和缓解期的免疫参数(包括淋巴细胞亚群)进行了测定。存在高免疫球蛋白血症E和免疫复合物。在疾病全过程中均可见抑制/细胞毒性(T8+)淋巴细胞比例低和辅助/抑制比例高,尽管免疫球蛋白水平和循环免疫复合物水平随治疗而下降。我们推测抑制细胞的缺乏可能在该综合征的发病机制中起作用。