Juers J A, Rogers R M, McCurdy J B, Cook W W
J Clin Invest. 1976 Aug;58(2):271-5. doi: 10.1172/JCI108468.
In vivo studies have shown a major role for the alveolar macrophage in the killing of inhaled bacteria. This contrasted with earlier work which showed a preservation of phagocytic properties but a loss of bactericidal capacity when alveolar macrophages were studied in vitro. Recently, alveolar lining material (ALM) from rats has been shown to enhance the in vitro bactericidal capacity of alveolar macrophages from homologous animals against Staphylococcus aureus. Utilizing a similar system, we have confirmed that rat alveolar macrophages do not kill S. aureus in vitro unless the bacteria have been incubated with rat ALM (R-ALM) before phagocytosis. In addition, human ALM (H-ALM) from 7 of 11 patients assayed showed an enhancement of bactericidal capacity by rat alveolar macrophages which was not significantly different from the results utilizing R-ALM. H-ALM from the other four patients gave results which differed significantly from results with H-ALM from the first seven patients and R-ALM (P less than 0.001). Preliminary results suggest that the factor enhancing the bactericidal capacity of rat alveolar macrophages is present in the lipid fraction of the ALM. Further characterization of the ALM is warranted in an effort to explain the enhancement of the bactericidal capacity of alveolar macrophages by most, but not all, H-ALM tested.
体内研究表明,肺泡巨噬细胞在杀灭吸入细菌方面起主要作用。这与早期的研究结果形成对比,早期研究显示,在体外研究肺泡巨噬细胞时,其吞噬特性得以保留,但杀菌能力丧失。最近,已证明大鼠的肺泡内衬物质(ALM)可增强同源动物肺泡巨噬细胞对金黄色葡萄球菌的体外杀菌能力。利用类似的系统,我们已证实,大鼠肺泡巨噬细胞在体外不会杀灭金黄色葡萄球菌,除非细菌在被吞噬之前已与大鼠ALM(R-ALM)孵育。此外,在检测的11例患者中,有7例患者的人ALM(H-ALM)显示大鼠肺泡巨噬细胞的杀菌能力增强,这与使用R-ALM的结果无显著差异。其他4例患者的H-ALM给出的结果与前7例患者的H-ALM和R-ALM的结果有显著差异(P小于0.001)。初步结果表明,增强大鼠肺泡巨噬细胞杀菌能力的因子存在于ALM的脂质部分。为了解释大多数(但不是全部)测试的H-ALM对肺泡巨噬细胞杀菌能力的增强作用,有必要对ALM进行进一步的特性分析。