Qian Chengyu, Fan Xueting, Wang Ruihuan, Cao Bin, Yu Jinjie, Luan Xiuli, Li Guilian, Jiang Yi, Li Machao, Zhao Xiuqin, Fang Danang, Wan Kanglin, Liu Haican, Lou Yongliang
School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou 325035, China.
State Key Laboratory for Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China.
Vaccines (Basel). 2023 Mar 7;11(3):609. doi: 10.3390/vaccines11030609.
Tuberculosis (TB) remains a serious global health problem. Despite the widespread use of the (BCG) vaccine, the primary factor for the TB pandemic and deaths is adult TB, which mainly result from endogenous reactivation of latent (MTB) infection. Improved new TB vaccines with eligible safety and long-lasting protective efficacy remains a crucial step toward the prevention and control of TB. In this study, five immunodominant antigens, including three early secreted antigens and two latency associated antigens, were used to construct a single recombinant fusion protein (Epera013f) and a protein mixture (Epera013m). When formulated with aluminum adjuvant, the two subunit vaccines Epera013m and Epera013f were administered to BALB/c mice. The humoral immune responses, cellular responses and MTB growth inhibiting capacity elicited after Epera013m and Epera013f immunization were analyzed. In the present study, we demonstrated that both the Epera013f and Epera013m were capable of inducing a considerable immune response and protective efficacy against H37Rv infection compared with BCG groups. In addition, Epera013f generated a more comprehensive and balanced immune status, including Th1, Th2 and innate immune response, over Epera013f and BCG. The multistage antigen complex Epera013f possesses considerable immunogenicity and protective efficacy against MTB infection ex vivo indicating its potential and promising applications in further TB vaccine development.
结核病(TB)仍然是一个严重的全球健康问题。尽管广泛使用了卡介苗(BCG),但结核病大流行和死亡的主要因素是成人结核病,这主要是由潜伏性结核分枝杆菌(MTB)感染的内源性重新激活引起的。开发具有合格安全性和持久保护效力的新型结核病疫苗仍然是预防和控制结核病的关键一步。在本研究中,使用了五种免疫显性抗原,包括三种早期分泌抗原和两种潜伏相关抗原,构建了一种单一重组融合蛋白(Epera013f)和一种蛋白混合物(Epera013m)。当与铝佐剂配制时,将两种亚单位疫苗Epera013m和Epera013f接种给BALB/c小鼠。分析了Epera013m和Epera013f免疫后引发的体液免疫反应、细胞反应和MTB生长抑制能力。在本研究中,我们证明,与卡介苗组相比,Epera013f和Epera013m均能够诱导针对H37Rv感染的显著免疫反应和保护效力。此外,与Epera013m和卡介苗相比,Epera013f产生了更全面和平衡的免疫状态,包括Th1、Th2和先天免疫反应。多阶段抗原复合物Epera013f在体外对MTB感染具有相当的免疫原性和保护效力,表明其在进一步的结核病疫苗开发中具有潜在的应用前景。