Ryan Nathan M, Hess Jessica A, Robertson Erica J, Tricoche Nancy, Turner Cheri, Davis Jenn, Petrovsky Nikolai, Ferguson Melissa, Rinaldi William J, Wong Valerie M, Shimada Ayako, Zhan Bin, Bottazzi Maria Elena, Makepeace Benjamin L, Gray Sean A, Carter Darrick, Lustigman Sara, Abraham David
Department of Microbiology and Immunology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Laboratory of Molecular Parasitology, Lindsey F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Vaccines (Basel). 2023 Jul 6;11(7):1212. doi: 10.3390/vaccines11071212.
Onchocerciasis remains a debilitating neglected tropical disease. Due to the many challenges of current control methods, an effective vaccine against the causative agent is urgently needed. Mice and cynomolgus macaque non-human primates (NHPs) were immunized with a vaccine consisting of a fusion of two protein antigens, -103 and -RAL-2 (-FUS-1), and three different adjuvants: Advax-CpG, alum, and AlT4. All vaccine formulations induced high antigen-specific IgG titers in both mice and NHPs. Challenging mice with L3 contained within subcutaneous diffusion chambers demonstrated that -FUS-1/Advax-CpG-immunized animals developed protective immunity, durable for at least 11 weeks. Passive transfer of sera, collected at several time points, from both mice and NHPs immunized with -FUS-1/Advax-CpG transferred protection to naïve mice. These results demonstrate that -FUS-1 with the adjuvant Advax-CpG induces durable protective immunity against in mice and NHPs that is mediated by vaccine-induced humoral factors.
盘尾丝虫病仍然是一种使人衰弱的被忽视热带病。由于当前控制方法面临诸多挑战,迫切需要一种针对病原体的有效疫苗。用由两种蛋白质抗原-103和-RAL-2融合而成的疫苗(-FUS-1)以及三种不同佐剂:Advax-CpG、明矾和AlT4对小鼠和食蟹猴非人灵长类动物(NHPs)进行免疫接种。所有疫苗制剂在小鼠和NHPs中均诱导出高抗原特异性IgG滴度。用皮下扩散室中所含的L3攻击小鼠表明,用-FUS-1/Advax-CpG免疫的动物产生了保护性免疫,持续至少11周。在多个时间点收集的来自用-FUS-1/Advax-CpG免疫的小鼠和NHPs的血清的被动转移将保护作用传递给了未免疫的小鼠。这些结果表明,-FUS-1与佐剂Advax-CpG在小鼠和NHPs中诱导出由疫苗诱导的体液因子介导的针对的持久保护性免疫。