Schickli Jeanne H, Dubovsky Filip, Tang Roderick S
Research Department, MedImmune, Mountain View, CA, USA.
Hum Vaccin. 2009 Sep;5(9):582-91. doi: 10.4161/hv.9131. Epub 2009 Sep 28.
RSV bronchiolitis is the leading cause of infant hospitalization in industrialized countries. There is an unmet need to prevent RSV lower respiratory tract infection in young infants. Although many vaccinology approaches, including live attenuated, viral and bacterial vectored and adjuvanted subunit vaccines have been evaluated in rodent and primate models there is currently no approved RSV vaccine. A vaccine candidate for RSV-naive infants must provide immunogenicity in the presence of maternally acquired antibodies, avoid enhanced disease and have minimal reactogenicity. Because live RSV infection does not potentiate for enhanced disease and elicits systemic and mucosal immune responses, live RSV vaccine candidates are currently preferred. Two live attenuated RSV vaccine candidates, rA2cpts248/404/1030/DeltaSH, a temperature sensitive RSV with a deletion of the SH gene, and rb/h PIV3/RSV F2 which has RSV F vectored into a bovine/human chimeric parainfluenza type 3 genome, have recently advanced into clinical studies.
呼吸道合胞病毒(RSV)细支气管炎是工业化国家婴儿住院的主要原因。预防幼儿RSV下呼吸道感染的需求尚未得到满足。尽管已经在啮齿动物和灵长类动物模型中评估了许多疫苗学方法,包括减毒活疫苗、病毒和细菌载体疫苗以及佐剂亚单位疫苗,但目前尚无获批的RSV疫苗。针对未感染过RSV的婴儿的候选疫苗必须在存在母体获得性抗体的情况下提供免疫原性,避免疾病加重且反应原性最小。由于活RSV感染不会导致疾病加重,且能引发全身和黏膜免疫反应,因此目前活RSV候选疫苗更受青睐。两种减毒活RSV候选疫苗,rA2cpts248/404/1030/DeltaSH(一种温度敏感型RSV,缺失SH基因)和rb/h PIV3/RSV F2(将RSV F基因导入牛/人嵌合3型副流感病毒基因组),最近已进入临床研究阶段。