Rodgers B C, Mims C A
J Med Virol. 1982;9(3):177-84. doi: 10.1002/jmv.1890090304.
Studies with animal models suggest that alveolar macrophages may be important cells in some respiratory virus infections, but little is known about the role of these cells in virus infections in man. In this study human alveolar macrophages were obtained by fibreoptic bronchoscopy and infected in vitro with a variety of influenza viruses. After infection with the NWS strain of influenza virus the haemagglutinin and nucleoprotein viral antigens were demonstrated in greater than 90% of cells at 24 h by immunofluorescence with specific antisera. There was no cytopathic effect at this time, and no virus release was detected by plaque assay of culture fluids on MDCK cells. Alveolar macrophages were also infected with a human vaccine strain (H1N1) of influenza virus and with two recent isolates (H1N1 and H3N2). In each case viral nucleoprotein antigen was produced in 10-20% of the cells by 24 h postincubation, but there was no release of infectious virus. There was no cytopathic effect and the phagocytosis of IgG-coated latex beads was unimpaired 24 h after in vitro infection.
对动物模型的研究表明,肺泡巨噬细胞可能是某些呼吸道病毒感染中的重要细胞,但对于这些细胞在人类病毒感染中的作用却知之甚少。在本研究中,通过纤维支气管镜获取人类肺泡巨噬细胞,并在体外使其感染多种流感病毒。用NWS株流感病毒感染后,在24小时时,用特异性抗血清通过免疫荧光法在超过90%的细胞中检测到了血凝素和核蛋白病毒抗原。此时没有细胞病变效应,通过在MDCK细胞上对培养液进行空斑试验也未检测到病毒释放。肺泡巨噬细胞还用一种人类流感疫苗株(H1N1)以及两种近期分离株(H1N1和H3N2)进行了感染。在每种情况下,孵育24小时后,10%-20%的细胞产生了病毒核蛋白抗原,但未检测到有感染性病毒的释放。没有细胞病变效应,体外感染24小时后,IgG包被的乳胶珠的吞噬作用未受损害。