Pringle C R
Bull World Health Organ. 1987;65(2):133-7.
Many of the common respiratory illnesses of infancy and childhood are caused by viruses of the Paramyxoviridae family, in particular measles virus, respiratory syncytial (RS) virus and parainfluenzavirus type 3 (PI3). Effective measles vaccine was developed by classical methods, but these same methods have failed to provide vaccines to control RS and PI3 virus infections. The WHO Programme for Vaccine Development was initiated in 1983 to encourage the application of the new biotechnologies to continuing problems, such as the acute virus-induced respiratory diseases of childhood. At a meeting of research workers held in July 1986 under the auspices of this programme, renewed optimism was expressed concerning the prospects for immunoprophylaxis of RS virus-induced disease. Animal models are now available for evaluation of the immunogenic potential of candidate vaccines. Vaccinia/RS recombinant viruses have been produced which have allowed the immunogenic properties of individual RS virus proteins to be defined. Complete protection without the exacerbation of disease, which earlier had accompanied the use of formalin-inactivated vaccines, has been achieved in animals immunized with vaccinia virus recombinants expressing the F protein; partial protection was obtained using G protein gene vectors. PI3 appears to be an inherently stable virus and evidence from animal experiments suggests that bovine PI3 might be suitable for use as a live vaccine in man.
婴幼儿时期的许多常见呼吸道疾病是由副粘病毒科的病毒引起的,尤其是麻疹病毒、呼吸道合胞(RS)病毒和3型副流感病毒(PI3)。有效的麻疹疫苗是通过经典方法研制出来的,但同样的方法未能提供控制RS和PI3病毒感染的疫苗。世界卫生组织疫苗开发计划于1983年启动,旨在鼓励将新生物技术应用于一些持续性问题,比如儿童急性病毒诱发的呼吸道疾病。在该计划主持下于1986年7月召开的一次研究人员会议上,人们对RS病毒诱发疾病的免疫预防前景再次表达了乐观态度。现在已有动物模型可用于评估候选疫苗的免疫原性潜力。已经制备出痘苗/RS重组病毒,这使得能够确定单个RS病毒蛋白的免疫原性特性。在用表达F蛋白的痘苗病毒重组体免疫的动物中,实现了完全保护且不会加剧疾病,而早期使用福尔马林灭活疫苗时曾出现疾病加剧的情况;使用G蛋白基因载体获得了部分保护。PI3似乎是一种本质上稳定的病毒,动物实验的证据表明牛PI3可能适合用作人类的活疫苗。