Exogenous surfactant therapy: newer developments

Thierry Lacaze-Masmonteil
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引用次数: 16

Abstract

There are numerous pulmonary conditions in which qualitative or quantitative anomalies of the surfactant system have been demonstrated. In premature newborns with immature lungs, a functional deficit in surfactant is the main physiopathologic mechanism of the neonatal respiratory distress syndrome (RDS). Since the landmark pilot study of Fujiwara, published more than 20 years ago, the efficacy of exogenous surfactant for the treatment of neonatal RDS has been established by numerous controlled studies and meta-analyses. Promising results have also been reported in infants suffering from other lung disorders in which endogenous surfactant function is compromised. Enlightened by a growing insight into both the structure and function of the different surfactant components, a new generation of synthetic surfactants has been developed. Various complementary approaches have confirmed the fundamental role of the two hydrophobic proteins, SP-B and SP-C, in the surfactant system, thus opening the way to the design of analogues, either by chemical synthesis or expression in a prokaryotic system. These peptide-containing synthetic surfactant preparations are presently undergoing clinical trials, and may eventually replace the animal-derived surfactants currently used for the treatment of RDS.

外源性表面活性剂治疗:最新进展
在许多肺部疾病中,表面活性剂系统的定性或定量异常已被证实。在肺功能不成熟的早产儿中,表面活性剂的功能缺陷是新生儿呼吸窘迫综合征(RDS)的主要生理病理机制。自20多年前发表具有里程碑意义的Fujiwara试点研究以来,外源性表面活性剂治疗新生儿RDS的疗效已被大量对照研究和荟萃分析所证实。在患有内源性表面活性剂功能受损的其他肺部疾病的婴儿中也报道了有希望的结果。随着人们对不同表面活性剂组分的结构和功能的深入了解,新一代的合成表面活性剂已经被开发出来。各种互补的方法已经证实了SP-B和SP-C这两种疏水蛋白在表面活性剂体系中的基本作用,从而为通过化学合成或在原核系统中表达设计类似物开辟了道路。这些含有肽的合成表面活性剂制剂目前正在进行临床试验,并可能最终取代目前用于治疗RDS的动物源性表面活性剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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