Department of Microbiology, College of Basic Medical Sciences, The Fourth Military Medical University, Shaanxi Province, China.
Department of Microbiology, College of Basic Medical Sciences, The Fourth Military Medical University, Shaanxi Province, China.
Microb Pathog. 2018 Dec;125:84-92. doi: 10.1016/j.micpath.2018.09.009. Epub 2018 Sep 6.
Tuberculosis is chronic infectious disease caused by Mycobacterium tuberculosis (M.tb) that is prevalent worldwide. Several specific antigens, such as Antigen 85B (Ag85B) and 6 kDa early secretory antigenic target (ESAT-6) protein of M.tb, are listed as some of the candidate subunit vaccines against M.tb. ESAT-6, as a virulent factor and differential gene in M.tb, shows insufficient immunogenicity in animal model. In order to investigate the ways to improve the immunogenicity of ESAT-6, we immunized ESAT-6 by subcutaneous and intramuscular routes with different adjuvants. We found that ESAT-6 immunized alone did not induce significant humoral immunity in both immunization routes. However, subcutaneous immunization of ESAT-6 plus incomplete Freund's adjuvant can induce a significant humoral immune response, enhanced proliferation and elevated secretion of IFN-γ from splenocytes. Intramuscular immunization of ESAT-6 plus adjuvant aluminum salt or poly(I:C) did not enhance humoral and cellular immune responses. Therefore, it is concluded that immunization of ESAT-6 subcutaneously plus incomplete Freund's adjuvant induces stronger humoral and cellular immune responses, which can be considered of ESAT-6 as a subunit vaccine in further research against tuberculosis.
结核病是由结核分枝杆菌(M.tb)引起的慢性传染病,在全球广泛流行。几种特定的抗原,如抗原 85B(Ag85B)和结核分枝杆菌的 6kDa 早期分泌抗原靶(ESAT-6)蛋白,被列为针对结核分枝杆菌的候选亚单位疫苗之一。ESAT-6 作为结核分枝杆菌的毒力因子和差异基因,在动物模型中表现出免疫原性不足。为了研究提高 ESAT-6 免疫原性的方法,我们用不同的佐剂通过皮下和肌肉途径免疫 ESAT-6。我们发现 ESAT-6 单独免疫在两种免疫途径中均未诱导出明显的体液免疫。然而,ESAT-6 加不完全弗氏佐剂的皮下免疫可诱导出明显的体液免疫反应,增强了脾细胞的增殖和 IFN-γ的分泌。ESAT-6 加佐剂铝盐或聚肌苷酸的肌肉内免疫并没有增强体液和细胞免疫反应。因此,结论是 ESAT-6 皮下免疫加不完全弗氏佐剂可诱导更强的体液和细胞免疫反应,可以考虑将 ESAT-6 作为进一步研究结核病的亚单位疫苗。