Godding V, Vaerman J P, Sibille Y
Experimental Medicine Unit, UCL St. Luc, Brussel, Belgium.
Acta Otorhinolaryngol Belg. 2000;54(3):255-61.
Mucosal immune mechanisms in the airways are the first specific line of defense, protecting the body from pathogens. The respiratory epithelium actively transports locally produced dimeric IgA in the respiratory secretions by transcytosis, through the pIgR. S-IgA production therefore requires epithelial integrity. S-IgA at the epithelial level is active in several non-inflammatory pathways including intracellular neutralization of virus, antigen excretion, binding to bacterial adhesins. Local IgA production is regulated by various growth factors and cytokines of both epithelial and non-epithelial origin. The respiratory epithelium is thought to play a crucial role in this process. In addition, in chronic airway inflammation, IgA production demonstrates a correlation with eosinophil activation both in vitro and in vivo. While increased IgA and S-IgA production is reported in asthmatics, decreased SC production has been documented in CF and COPD patients, further impairing their local defense mechanisms.
气道中的黏膜免疫机制是第一道特异性防线,保护身体免受病原体侵害。呼吸道上皮细胞通过多聚免疫球蛋白受体(pIgR)的转胞吞作用,主动转运呼吸道分泌物中局部产生的二聚体IgA。因此,分泌型IgA(S-IgA)的产生需要上皮的完整性。上皮水平的S-IgA在多种非炎症途径中发挥作用,包括病毒的细胞内中和、抗原排泄、与细菌黏附素结合。局部IgA的产生受上皮和非上皮来源的多种生长因子和细胞因子调节。呼吸道上皮细胞被认为在这一过程中起关键作用。此外,在慢性气道炎症中,IgA的产生在体外和体内均与嗜酸性粒细胞活化相关。虽然哮喘患者中报道了IgA和S-IgA产生增加,但在囊性纤维化(CF)和慢性阻塞性肺疾病(COPD)患者中已记录到分泌成分(SC)产生减少,进一步损害了他们的局部防御机制。