Univ. Lille, CNRS, Inserm, CHU Lille, Institute Pasteur de Lille, U1019-UMR9017-CIIL-Centre for Infection and Immunity of Lille, F-59000 Lille, France.
Univ. Lille, CNRS, Inserm, CHU Lille, Institute Pasteur de Lille, U1019-UMR9017-CIIL-Centre for Infection and Immunity of Lille, F-59000 Lille, France.
Vaccine. 2022 Mar 8;40(11):1555-1562. doi: 10.1016/j.vaccine.2021.01.025. Epub 2021 Jan 25.
BPZE1 is a live attenuated vaccine against infection by Bordetella pertussis, the causative agent of whooping cough. It was previously shown that BPZE1 provides heterologous protection in mouse models of disease caused by unrelated pathogens, such as influenza virus and respiratory syncytial virus. Protection was also observed in mouse models of asthma and contact dermatitis. In this study, we demonstrate that BPZE1 also displays protection against an unrelated bacterial pathogen in a mouse model of invasive pneumococcal disease mediated by Streptococcus pneumoniae. While a single administration of BPZE1 provided no protection, two doses of 10 colony-forming units of BPZE1 given in a three-week interval protected against mortality, lung colonization and dissemination in both BALB/c and C57BL/6 mice. Unlike for the previously reported influenza challenge model, protection was short-lived, and waned within days after booster vaccination. Formaldehyde-killed BPZE1 protected only when administered following a live prime, indicating that priming requires live BPZE1 for protection. Protection against mortality was directly linked to substantially decreased bacterial dissemination in the blood and was lost in MyD88 knock-out mice, demonstrating the role of the innate immune system in the mechanism of protection. This is the first report on a heterologous protective effect of the live BPZE1 vaccine candidate against an unrelated bacterial infection.
BPZE1 是一种针对百日咳博德特氏菌感染的减毒活疫苗,百日咳博德特氏菌是百日咳的病原体。先前的研究表明,BPZE1 可在流感病毒和呼吸道合胞病毒等无关病原体引起的疾病的小鼠模型中提供异源保护。在哮喘和接触性皮炎的小鼠模型中也观察到了保护作用。在这项研究中,我们证明 BPZE1 还可在肺炎链球菌介导的侵袭性肺炎球菌病小鼠模型中提供针对无关细菌病原体的保护。虽然单次给予 BPZE1 没有提供保护,但在三周的间隔内给予两次 10 个集落形成单位的 BPZE1 可保护 BALB/c 和 C57BL/6 小鼠免受死亡率、肺部定植和传播的影响。与先前报道的流感挑战模型不同,保护作用是短暂的,在加强疫苗接种后几天内减弱。甲醛灭活的 BPZE1 仅在活疫苗接种后给予时才提供保护,表明启动需要活的 BPZE1 才能提供保护。对死亡率的保护与血液中细菌传播的大量减少直接相关,并且在 MyD88 敲除小鼠中丧失,证明了先天免疫系统在保护机制中的作用。这是关于活的 BPZE1 疫苗候选物对无关细菌感染的异源保护作用的首次报道。