Lanzhou Center for Tuberculosis Research & Institute of Pathogenic Biology, School of Basic Medical Sciences, Lanzhou University, Lanzhou, China.
PLoS One. 2013 Aug 15;8(8):e72745. doi: 10.1371/journal.pone.0072745. eCollection 2013.
To search for more effective tuberculosis (TB) subunit vaccines, antigens expressed in different growth stages of Mycobacterium tuberculosis (M. tuberculosis), such as RpfE (Rv2450c) produced in the stage of resuscitation, Mtb10.4 (Rv0288), Mtb8.4 (Rv1174c), ESAT6 (Rv3875), Ag85B (Rv1886c) mainly secreted by replicating bacilli, and HspX (Rv2031c) highly expressed in dormant bacilli, were selected to construct six fusion proteins: ESAT6-Ag85B-MPT64190-198-Mtb8.4 (EAMM), Mtb10.4-HspX (MH), ESAT6-Mtb8.4, Mtb10.4-Ag85B, ESAT6-Ag85B, and ESAT6-RpfE. The six fusion proteins were separately emulsified in an adjuvant composed of N,N'-dimethyl-N, N'-dioctadecylammonium bromide (DDA), polyribocytidylic acid (poly I:C) and gelatin to construct subunit vaccines, and their protective effects against M. tuberculosis infection were evaluated in C57BL/6 mice. Furthermore, the boosting effects of EAMM and MH in the adjuvant of DDA plus trehalose 6,6'-dimycolate (TDM) on BCG-induced immunity were also evaluated. It was found that the six proteins were stably produced in E. coli and successfully purified by chromatography. Among them, EAMM presented the most effective protection against M. tuberculosis. Interestingly, the mice that received EAMM+MH had significantly lower bacterial counts in the lungs and spleens than the single protein vaccinated groups, and had the same effect as those that received BCG. In addition, EAMM and MH could improve BCG-primed protective efficacy against M. tuberculosis infection in mice. In conclusion, the combination of EAMM and MH containing antigens from both replicating and dormant stages of the bacilli could induce robust immunity against M. tuberculosis infection in mice and may serve as promising subunit vaccine candidate.
为了寻找更有效的结核病(TB)亚单位疫苗,人们选择了在结核分枝杆菌(M. tuberculosis)不同生长阶段表达的抗原,如复苏阶段产生的 RpfE(Rv2450c)、Mtb10.4(Rv0288)、Mtb8.4(Rv1174c)、ESAT6(Rv3875)、Ag85B(Rv1886c)主要由复制菌分泌,以及休眠菌中高表达的 HspX(Rv2031c),构建了 6 种融合蛋白:ESAT6-Ag85B-MPT64190-198-Mtb8.4(EAMM)、Mtb10.4-HspX(MH)、ESAT6-Mtb8.4、Mtb10.4-Ag85B、ESAT6-Ag85B 和 ESAT6-RpfE。将这 6 种融合蛋白分别用由 N,N'-二甲基-N,N'-二辛基溴化铵(DDA)、聚肌苷酸(poly I:C)和明胶组成的佐剂乳化,构建亚单位疫苗,并在 C57BL/6 小鼠中评估其对结核分枝杆菌感染的保护作用。此外,还评估了 EAMM 和 MH 在 DDA 加海藻糖 6,6'-二没食子酸酯(TDM)佐剂中对 BCG 诱导免疫的增强作用。结果发现,这 6 种蛋白在大肠杆菌中稳定表达,并通过色谱法成功纯化。其中,EAMM 对结核分枝杆菌的保护作用最为有效。有趣的是,与单一蛋白接种组相比,接受 EAMM+MH 治疗的小鼠肺部和脾脏的细菌载量明显更低,与接受 BCG 治疗的小鼠效果相同。此外,EAMM 和 MH 可以提高 BCG 初免小鼠对结核分枝杆菌感染的保护效果。综上所述,EAMM 和 MH 联合含有复制和休眠阶段细菌抗原的组合可在小鼠中诱导针对结核分枝杆菌感染的强大免疫,可能成为有前途的亚单位疫苗候选物。