Benoit A, Huang Y, Proctor J, Rowden G, Anderson R
Departments of Microbiology and Immunology, Dalhousie University, Halifax, Nova Scotia, Canada.
Clin Exp Immunol. 2006 Jul;145(1):147-54. doi: 10.1111/j.1365-2249.2006.03114.x.
Little is known about the identities and roles of antigen-presenting cells upon exposure to antigens of respiratory syncytial virus (RSV). Here, we focused on elucidating the importance of alveolar macrophages in conferring protective immunity in mice administered a liposome-encapsulated recombinant fragment of the RSV G protein. Mice were depleted of alveolar macrophages by intranasal inoculation of liposome-encapsulated dichloromethylenediphosphonic acid (DMDP). Mice depleted of alveolar macrophages prior to immunization developed reduced levels of serum RSV-neutralizing antibody and showed dramatically impaired protection against RSV challenge. The severity of interstitial inflammation was also markedly reduced in macrophage-depleted mice. In conclusion, this study demonstrates a pivotal role for alveolar macrophages during exposure to liposome-encapsulated RSV antigen in initiating both protective and histopathological responses against RSV.
关于抗原呈递细胞在接触呼吸道合胞病毒(RSV)抗原后的身份和作用,人们了解甚少。在此,我们着重阐明肺泡巨噬细胞在给予脂质体包裹的RSV G蛋白重组片段的小鼠中赋予保护性免疫的重要性。通过鼻内接种脂质体包裹的二氯亚甲基二膦酸(DMDP)使小鼠的肺泡巨噬细胞耗竭。免疫前肺泡巨噬细胞耗竭的小鼠血清RSV中和抗体水平降低,并且对RSV攻击的保护作用显著受损。巨噬细胞耗竭的小鼠间质炎症的严重程度也明显降低。总之,本研究证明了肺泡巨噬细胞在接触脂质体包裹的RSV抗原期间在引发针对RSV的保护性和组织病理学反应中起关键作用。