Ekdahl K, Truedsson L, Sjöholm A G, Braconier J H
Department of Infectious Diseases, Lund University Hospital, Sweden.
Scand J Infect Dis. 1995;27(2):111-7. doi: 10.3109/00365549509018989.
Complement deficiencies are known to be associated with increased susceptibility to bacterial infections. In the present study we investigated 80 patients with either a history of pneumococcal bacteremic infection, or recurrent pneumonia, or both. Hemolytic screening tests for complement deficiency were performed and serum concentrations of C1q, C1s, C2, C3, C4, C4 isotypes, factor B, factor D, and properdin were determined. Complete deficiencies of single complement proteins were not found. 10 patients (12%) had a C4 isotype deficiency, but the frequency of homozygous C4A and C4B deficiency was not significantly increased. Seven patients (9%) had hypocomplementemia with low concentrations of at least 2 complement proteins. One of these patients had profound depletion of classical pathway components and findings suggesting acquired C1 esterase inhibitor deficiency. 16 patients (20%) had minor complement aberrations. A majority of the patients with hypocomplementemia suffered from other conditions associated with pneumococcal infections. However, impaired complement function could be a significant predisposing factor in some patients with invasive pneumococcal infections or recurrent pneumonia.
已知补体缺陷与细菌感染易感性增加有关。在本研究中,我们调查了80例有肺炎球菌菌血症感染史、复发性肺炎病史或两者兼有的患者。进行了补体缺陷的溶血筛查试验,并测定了C1q、C1s、C2、C3、C4、C4同种型、B因子、D因子和备解素的血清浓度。未发现单一补体蛋白的完全缺陷。10例患者(12%)存在C4同种型缺陷,但纯合子C4A和C4B缺陷的频率未显著增加。7例患者(9%)存在补体血症,至少2种补体蛋白浓度较低。其中1例患者经典途径成分严重耗竭,并有提示获得性C1酯酶抑制剂缺乏的表现。16例患者(20%)存在轻微的补体异常。大多数补体血症患者患有与肺炎球菌感染相关的其他疾病。然而,补体功能受损可能是一些侵袭性肺炎球菌感染或复发性肺炎患者的重要易感因素。