Surfactant protein A - Regulation of innate and adaptive immune responses in lung inflammation

被引:47
|
作者
Wright, JR
Borron, P
Brinker, KG
Folz, RJ
机构
[1] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
关键词
D O I
10.1165/ajrcmb.24.5.f208
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although the bulk of available studies demonstrate a role for SP-A and SP-D in pulmonary innate immunity, a growing body of literature supports the possibility that the lung collectins directly mediate functions of cells of the adaptive immune response. The report by Yang and coworkers (1) lends credence to the hypothesis that SP-A and SP-D may mediate cross-talk between innate and adaptive immunity in the lungs, a prospect that requires further investigation. The current study also raises the provocative possibility that SP-A containing surfactant preparations may be important for treatment of idiopathic pneumonitits syndrome and other pulmonary inflammatory diseases. Currently, neither SP-A nor SP-D are components of the surfactant replacement therapies that are routinely used to treat infant respiratory distress syndrome or in the surfactant preparations that have been tested as therapies for acute respiratory distress syndrome, an inflammatory disease associated with deficiencies in SP-A and SP-D (60) as well as other surfactant components (61-63). Although there are still many unanswered questions about the functions of these proteins, the rationale is building for considering these proteins as therapies for lung inflammation.
引用
收藏
页码:513 / 517
页数:5
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