Ottolini MG
Department of Pediatrics, F. Edward Hébert School of Medicine, The Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814-4799, USA. E-mail:
Curr Infect Dis Rep. 2000 Apr;2(2):121-129. doi: 10.1007/s11908-000-0024-x.
Viral and bacterial respiratory infections remain the number one cause of infectious disease-related deaths around the world. In the past, vaccines were often created by repeatedly passing laboratory cultures to develop attenuated strains or simply by inactivating live cultures of pathogens. A variety of new and innovative technologies are being applied to develop vaccines against the more elusive pathogens. A variety of protein conjugates have been used to greatly enhance the immunogenicity of Haemophilus influenzae type B vaccine, and are now being employed for new pneumococcal and meningococcal vaccines. Live attenuated vaccine strains of respiratory syncytial virus and influenza, which induce protective immunity through localized replication in the nasopharynx, may soon be available for routine use. Future innovations may include genetic vaccines that introduce DNA into host cells to produce specific protective antigens, along with a desired cytokine response to induce a protective immune response.
病毒和细菌引起的呼吸道感染仍然是全球与传染病相关死亡的首要原因。过去,疫苗通常通过反复传代实验室培养物来培育减毒株,或者仅仅通过灭活病原体的活培养物来制备。各种新的创新技术正被应用于研发针对更难捉摸病原体的疫苗。多种蛋白质偶联物已被用于大幅增强B型流感嗜血杆菌疫苗的免疫原性,目前正被用于新型肺炎球菌和脑膜炎球菌疫苗。呼吸道合胞病毒和流感的减毒活疫苗株通过在鼻咽部局部复制诱导保护性免疫,可能很快可供常规使用。未来的创新可能包括基因疫苗,即将DNA导入宿主细胞以产生特定的保护性抗原,同时引发所需的细胞因子反应以诱导保护性免疫反应。