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肺表面活性物质对自然杀伤细胞及抗体依赖性细胞毒性的免疫调节作用。

Immunomodulatory effects of pulmonary surfactant on natural killer cell and antibody-dependent cytotoxicity.

作者信息

Wilsher M L, Hughes D A, Haslam P L

机构信息

Cell Biology Unit, Cardiothoracic Institute, London.

出版信息

Clin Exp Immunol. 1988 Dec;74(3):465-70.

Abstract

Alveolar natural killer (NK) cells are functionally weak compared to their blood and interstitial counterparts. Having previously demonstrated that pulmonary surfactant suppresses lymphocyte responses to a variety of stimuli we sought in this study to determine if surfactant exerts a similar suppressive effect on cytotoxic function. Lipids were purified from the bronchoalveolar lavage (BAL) fluid from normal human volunteers. Human peripheral blood lymphocytes (n = 10 subjects) were cultured overnight in the presence or absence of purified BAL lipids (0.2 mg/ml), or pure preparations of phosphatidylcholine (PC), phosphatidylethanolamine (PE), and phosphatidylglycerol (PG) (0.4 mg/ml). Standard NK and antibody-dependent cytotoxicity (ADCC) assays were performed using K562 and Chang target cells. The pooled BAL lipids significantly suppressed both NK (P less than 0.01) and ADCC (P = 0.01) activity in a dose-dependent manner. Whereas pure PC did not exert a significant effect, PG significantly suppressed (P less than 0.01) and PE significantly enhanced (P less than 0.01) both cytotoxic functions. There was no change in the expression of leu 7 or 11b antigens by lymphocytes after culture in BAL lipids. These results suggest that under normal circumstances pulmonary surfactant may suppress alveolar cytotoxic responses but that imbalances in the phospholipid profile might affect this immunoregulatory property.

摘要

与血液和间质中的自然杀伤(NK)细胞相比,肺泡NK细胞的功能较弱。此前我们已经证明肺表面活性剂会抑制淋巴细胞对多种刺激的反应,在本研究中,我们试图确定表面活性剂是否对细胞毒性功能也有类似的抑制作用。从正常人类志愿者的支气管肺泡灌洗(BAL)液中纯化脂质。将人类外周血淋巴细胞(n = 10名受试者)在存在或不存在纯化的BAL脂质(0.2 mg/ml)或磷脂酰胆碱(PC)、磷脂酰乙醇胺(PE)和磷脂酰甘油(PG)的纯制剂(0.4 mg/ml)的情况下培养过夜。使用K562和Chang靶细胞进行标准NK和抗体依赖性细胞毒性(ADCC)测定。合并的BAL脂质以剂量依赖性方式显著抑制NK(P < 0.01)和ADCC(P = 0.01)活性。而纯PC没有显著作用,PG显著抑制(P < 0.01)且PE显著增强(P < 0.01)两种细胞毒性功能。淋巴细胞在BAL脂质中培养后,leu 7或11b抗原的表达没有变化。这些结果表明,在正常情况下,肺表面活性剂可能会抑制肺泡细胞毒性反应,但磷脂谱的失衡可能会影响这种免疫调节特性。

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