Rossman C, Dodlovich J, Dodlovich M, Wilson W, Newhouse M
J Pediatr. 1977 Apr;90(4):579-84. doi: 10.1016/s0022-3476(77)80370-3.
Studies were performed to demonstrate possibly cystic fibrosis-related inhibition of mucociliary clearance in man. Topical application of normal serum or of CF serum did not inhibit in vivo nasal MCC. Induction of local inflammation by topical anti-IgE-reduced nasal MCC in CF subjects, but increased MCC in normal individuals. Furthermore, nasal MCC was inhibited in normal patients by CF serum but not normal serum, applied to the anti-IgE-treated nasal mucosa. These observations are consistent with the hypothesis that CF serum inhibits MCC in vivo in the inflamed mucosa.
开展了多项研究以证明人类中可能与囊性纤维化相关的黏液纤毛清除功能抑制。局部应用正常血清或囊性纤维化血清在体内并未抑制鼻腔黏液纤毛清除功能。局部应用抗IgE减轻了囊性纤维化患者的鼻腔黏液纤毛清除功能,但增加了正常个体的该功能。此外,将囊性纤维化血清而非正常血清应用于经抗IgE处理的鼻黏膜时,正常患者的鼻腔黏液纤毛清除功能受到抑制。这些观察结果与以下假设一致,即囊性纤维化血清在体内抑制炎症黏膜中的黏液纤毛清除功能。