Strayer D S, Merritt T A, Lwebuga-Mukasa J, Hallman M
Am J Pathol. 1986 Feb;122(2):353-62.
The authors sought to determine whether treatment of respiratory distress syndrome (RDS) with human surfactant resulted in the formation of detectable circulating immune complexes. Preterm infants with severe RDS were divided into two groups: one group received human surfactant by intratracheal instillation and the other group did not. Both groups received ventilatory management involving intermittent mandatory ventilation. Plasma samples were drawn from these babies prior to treatment and at intervals thereafter. The authors developed an ELISA assay specific for surfactant-anti-surfactant immune complexes and analyzed the plasma samples for such immune complexes. Complement levels were also measured. They found that with time plasma from RDS infants in both groups showed evidence of surfactant-anti-surfactant immune complex formation. The concentrations of immune complexes generally peaked within the first week of life and then appeared to diminish over 1-4 weeks after birth in RDS infants. There was no evidence at any time in either group of immune-complex-mediated injury or of decreased serum complement levels. It is concluded that circulating immune complexes between surfactant and antibodies to surfactant are probably found in most neonates with respiratory distress syndrome, that they do not produce pulmonary damage detectable by clinical and serologic means, and that treatment of neonatal RDS with human surfactant similarly does not produce lung injury as determined with these techniques.
作者试图确定用人肺表面活性物质治疗呼吸窘迫综合征(RDS)是否会导致可检测到的循环免疫复合物形成。患有严重RDS的早产儿被分为两组:一组通过气管内滴注接受人肺表面活性物质,另一组不接受。两组均接受包括间歇强制通气的通气管理。在治疗前及之后的不同时间从这些婴儿身上采集血浆样本。作者开发了一种针对肺表面活性物质-抗肺表面活性物质免疫复合物的酶联免疫吸附测定(ELISA),并分析血浆样本中的此类免疫复合物。同时也测量了补体水平。他们发现,随着时间推移,两组RDS婴儿的血浆都显示出肺表面活性物质-抗肺表面活性物质免疫复合物形成的迹象。免疫复合物的浓度通常在出生后的第一周内达到峰值,然后在RDS婴儿出生后的1 - 4周内似乎逐渐下降。两组在任何时候都没有免疫复合物介导的损伤证据或血清补体水平降低的证据。得出的结论是,大多数患有呼吸窘迫综合征的新生儿体内可能存在肺表面活性物质与抗肺表面活性物质抗体之间的循环免疫复合物,它们不会产生通过临床和血清学方法可检测到的肺损伤,并且用人肺表面活性物质治疗新生儿RDS同样不会产生用这些技术确定的肺损伤。