Schiøtz P O, Nielsen H, Høiby N, Glikmann G, Svehag S E
Acta Pathol Microbiol Scand C. 1978 Feb;86(1):37-40. doi: 10.1111/j.1699-0463.1978.tb02555.x.
12 cystic fibrosis (CF) patients chronically infected with mucoid P. aeruginosa and presenting multiple precipitins in serum against this bacterium and 12 patients without P. aeruginosa infection were examined for occurrence of soluble immune complexes in their sputum sol phase by a complement consumption assay and a solid phase rheumatoid factor binding assay. The correlation between the results obtained in the two assays was significant (r = 0.625, p less than 0.01). The patients chronically infected with P. aeruginosa showed a significantly (p less than 0.01) higher frequency of immune complex activity in their sputum sol phase, as compared to the patients without P. aeruginosa lung infection. These findings point to the possibility that chronic lung infection with mucoid P. aeruginosa in CF may be an immune complex disease.
对12名长期感染黏液型铜绿假单胞菌且血清中针对该细菌呈现多种沉淀素的囊性纤维化(CF)患者,以及12名未感染铜绿假单胞菌的患者,通过补体消耗试验和固相类风湿因子结合试验检测其痰液可溶性相中的可溶性免疫复合物。两种试验结果之间的相关性显著(r = 0.625,p < 0.01)。与未发生铜绿假单胞菌肺部感染的患者相比,长期感染铜绿假单胞菌的患者痰液可溶性相中免疫复合物活性频率显著更高(p < 0.01)。这些发现表明,CF患者中黏液型铜绿假单胞菌的慢性肺部感染可能是一种免疫复合物疾病。