Kim Hyeong Won, Shin Seokwon, Park So Hui, Park Jong-Hyeon, Kim Su-Mi, Lee Yoon-Hee, Lee Min Ja
Center for Foot-and-Mouth Disease Vaccine Research, Animal and Plant Quarantine Agency, Gimcheon-si, Gyeongsangbuk-do, Republic of Korea.
Front Immunol. 2024 Dec 11;15:1491043. doi: 10.3389/fimmu.2024.1491043. eCollection 2024.
Many countries use commercial foot-and-mouth disease (FMD) vaccines to prevent FMD pandemics, but these vaccines have disadvantages, such as repeated vaccinations due to the short persistence of antibody (Ab) titers and incomplete host defense despite high Ab titers. To address these shortcomings, we aimed to develop a novel FMD vaccine containing furfurman as an adjuvant.
To demonstrate the efficacy of the test vaccine, adaptive immunity was evaluated by measuring Ab and neutralizing Ab titers and host defense against viral infections in experimental and target animals. In addition, the expression levels of cytokines [interferon (IFN)α, IFNβ, IFNγ, interleukin (IL)-1β, IL-2, and IL-12p40] were evaluated at the early stages of vaccination to confirm the simultaneous induction of cellular and humoral immune responses induced by the test vaccine.
The groups that received vaccine containing furfurman showed a strong early, mid-term, and long-term immune response and host defense against viral infections compared to the control groups. The significant upregulation observed in cytokine levels in the furfurman group compared to those in the control groups strongly suggest that the test vaccine strengthens cellular immune response and effectively induces a humoral immune response.
Our study demonstrated that furfurman, as an FMD vaccine adjuvant, achieves long-lasting immunity and host defense against viral infections by eliciting potent cellular and humoral immune responses. Therefore, our findings contribute to the design of next-generation FMD vaccines and highlight the potential application of furfurman as an adjuvant for other viral diseases.
许多国家使用商业口蹄疫(FMD)疫苗来预防FMD大流行,但这些疫苗存在缺点,例如由于抗体(Ab)滴度持续时间短而需要重复接种,以及尽管Ab滴度高但宿主防御仍不完整。为了解决这些缺点,我们旨在开发一种含有糠醛的新型FMD疫苗。
为了证明试验疫苗的有效性,通过测量实验动物和目标动物中的Ab和中和Ab滴度以及针对病毒感染的宿主防御来评估适应性免疫。此外,在接种疫苗的早期阶段评估细胞因子[干扰素(IFN)α、IFNβ、IFNγ、白细胞介素(IL)-1β、IL-2和IL-12p40]的表达水平,以确认试验疫苗诱导的细胞免疫和体液免疫反应的同时诱导。
与对照组相比,接受含有糠醛疫苗的组在早期、中期和长期均表现出强烈的免疫反应和针对病毒感染的宿主防御。与对照组相比,糠醛组中细胞因子水平的显著上调强烈表明试验疫苗增强了细胞免疫反应并有效诱导了体液免疫反应。
我们的研究表明,糠醛作为FMD疫苗佐剂,通过引发强大的细胞免疫和体液免疫反应,实现了持久的免疫力和针对病毒感染的宿主防御。因此,我们的研究结果有助于下一代FMD疫苗的设计,并突出了糠醛作为其他病毒性疾病佐剂的潜在应用。