Kalina Warren V, Woolums Amelia R, Gershwin Laurel J
Department of Pathology, Microbiology, & Immunology, School of Veterinary Medicine, University of California, Davis, CA 95616, USA.
Vaccine. 2005 Aug 31;23(37):4625-30. doi: 10.1016/j.vaccine.2005.04.032.
Respiratory syncytial virus (RSV) causes severe respiratory disease in calves and human infants. In response to outbreaks, formalin inactivated (FI)-RSV vaccines were developed and found to exacerbate disease following a live RSV infection. We have reproduced vaccination induced disease enhancement in calves and screened various antibody isotypes in bronchoalveolar lavage fluid (BALF) from two studies: one with disease enhancement and another where moderate protection resulted from FI-bovine RSV (BRSV) vaccination. Semi-protected vaccinated calves produced BRSV-specific BALF IgG1, but not IgA and IgG2 prior to infection; whereas, calves with enhanced disease failed to develop BRSV-specific IgG1 in BALF. Ultimately, the formulation and delivery of RSV vaccines influences protective antibody levels in respiratory secretions.
呼吸道合胞病毒(RSV)可导致犊牛和人类婴儿患严重呼吸道疾病。为应对疫情,研发了福尔马林灭活(FI)-RSV疫苗,但发现其在活RSV感染后会加重病情。我们在犊牛中重现了疫苗接种引起的疾病增强现象,并在两项研究的支气管肺泡灌洗液(BALF)中筛选了各种抗体亚型:一项研究出现了疾病增强,另一项研究中FI-牛呼吸道合胞病毒(BRSV)疫苗接种产生了中度保护作用。半保护的接种疫苗犊牛在感染前产生了BRSV特异性BALF IgG1,但未产生IgA和IgG2;而疾病增强的犊牛未能在BALF中产生BRSV特异性IgG1。最终,RSV疫苗的配方和给药方式会影响呼吸道分泌物中的保护性抗体水平。