Institute for Cellular Therapeutics, University of Louisville, Louisville, KY 40202, United States; FasCure Therapeutics, LLC, Louisville, KY 40202, United States.
Institute for Cellular Therapeutics, University of Louisville, Louisville, KY 40202, United States.
Vaccine. 2019 Sep 10;37(38):5708-5716. doi: 10.1016/j.vaccine.2019.07.103. Epub 2019 Aug 12.
Yersinia pestis is the causative agent of plague and is a re-emerging pathogen that also has the potential as a biological weapon, necessitating the development of a preventive vaccine. Despite intense efforts for the last several decades, there is currently not a vaccine approved by the FDA. The rF1-V vaccine adjuvanted with Alhydrogel is a lead candidate subunit vaccine for plague and generates a strong Th2-mediate humoral response with a modest Th1 cellular response. As immune protection against Y. pestis requires both humoral and Th1 cellular responses, modifying the rF1-V subunit vaccine formulation to include a robust inducer of Th1 responses may improve efficacy. Thus, we reformulated the subunit vaccine to include SA-4-1BBL, an agonist of the CD137 costimulatory pathway and a potent inducer of Th1 response, and assessed its protective efficacy against pneumonic plague. We herein show for the first time a sex bias in the prophylactic efficacy of the Alhydrogel adjuvanted rF1-V vaccine, with female mice showing better protection against pneumonic plague than male. The sex bias for protection was irrespective of the generation of comparable levels of rF1-V-specific antibody titers and Th1 cellular responses in both sexes. The subunit vaccine reformulated with SA-4-1BBL generated robust Th1 cellular and humoral responses. A prime-boost vaccination scheme involving prime with rF1-V + Alhydrogel and boost with the rF1-V + SA-4-1BBL provided protection in male mice against pneumonic plague. In marked contrast, prime and boost with rF1-V reformulated with both adjuvants resulted in the loss of protection against pneumonic plague, despite generating high levels of humoral and Th1 cellular responses. While unexpected, these findings demonstrate the complexity of immune mechanisms required for protection. Elucidating mechanisms responsible for these differences in protection will help to guide the development of better prophylactic subunit vaccines effective against pneumonic plague.
鼠疫耶尔森菌是鼠疫的病原体,也是一种具有潜在生物武器能力的重现病原体,因此需要开发预防性疫苗。尽管过去几十年进行了大量努力,但目前还没有获得 FDA 批准的疫苗。用 Alhydrogel 佐剂的 rF1-V 疫苗是鼠疫的主要候选亚单位疫苗,可产生强烈的 Th2 介导的体液免疫应答,并伴有适度的 Th1 细胞免疫应答。由于对 Y. pestis 的免疫保护需要体液和 Th1 细胞免疫应答,因此,我们可以修改 rF1-V 亚单位疫苗的配方,使其包含一种强有力的 Th1 应答诱导剂,从而提高其疗效。因此,我们将亚单位疫苗重新配方,使其包含 SA-4-1BBL,这是一种 CD137 共刺激途径的激动剂,也是 Th1 应答的有效诱导剂,并评估其对肺鼠疫的保护效果。我们首次证明了 Alhydrogel 佐剂 rF1-V 疫苗在预防效果上存在性别差异,女性小鼠比男性小鼠对肺鼠疫的保护更好。这种保护的性别差异与两性中产生可比水平的 rF1-V 特异性抗体滴度和 Th1 细胞应答无关。用 SA-4-1BBL 重新配方的亚单位疫苗产生了强烈的 Th1 细胞和体液免疫应答。用 rF1-V+Alhydrogel 进行初免,然后用 rF1-V+SA-4-1BBL 进行加强的初免-加强免疫方案为雄性小鼠提供了针对肺鼠疫的保护。相比之下,用两种佐剂重新配方的 rF1-V 进行初免和加强免疫导致对肺鼠疫的保护丧失,尽管产生了高水平的体液和 Th1 细胞应答。虽然出人意料,但这些发现表明了保护所需的免疫机制的复杂性。阐明导致这些保护差异的机制将有助于指导针对肺鼠疫的更有效的预防性亚单位疫苗的开发。