Alveolar macrophages, surfactant lipids, and surfactant protein B regulate the induction of immune responses via the airways

被引:30
作者
van Iwaarden, JF
Claassen, E
Jeurissen, SHM
Haagsman, HP
Kraal, G
机构
[1] Erasmus Univ, Pediat Lab, NL-3015 GE Rotterdam, Netherlands
[2] Vrije Univ Amsterdam, Fac Med, Dept Cell Biol & Immunol, NL-1081 HV Amsterdam, Netherlands
[3] Univ Utrecht, Inst Anim Sci & Hlth, Utrecht, Netherlands
[4] Univ Utrecht, Vet Biochem Lab, NL-3508 TD Utrecht, Netherlands
关键词
D O I
10.1165/ajrcmb.24.4.4239
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
The influences of alveolar macrophages (AM) and pulmonary surfactant on the induction of immune responses via the airways were assessed. Mice were depleted of their AM by intratracheal instillation of multilamellar vesicles containing dichloromethylene-diphosphonate followed by intratracheal instillation of a T cell-dependent antigen, trinitrophenyl-keyhole limpet hemocyanin, in vesicles of various compositions. The primary immune response was determined in the spleen of these animals using an ELI-Spot assay. The secondary immune responses in the sera of the mice were assessed using enzyme-linked immunosorbent assays. An immune response was detected in animals depleted of their AM and intratracheally instilled with antigen in small unilamellar vesicles consisting of either phosphatidylcholine cholesterol or surfactant lipids. Incorporation of surfactant protein (SP)-B in the antigen vesicles enhanced the immune response, whereas SP-A or SP-C in the antigen vesicle did not have an effect. Strikingly, intratracheal instillation of SP-B containing antigen vesicles can induce an immunoglobulin M immune response in mice without depletion of AM. These results indicate that SP-B containing vesicles can enhance the induction of immune responses via the airways and further illustrate the important roles of both AM and pulmonary surfactant in the pulmonary immune system.
引用
收藏
页码:452 / 458
页数:7
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