Jiang Xinpeng, Yu Meiling, Qiao Xinyuan, Liu Min, Tang Lijie, Jiang Yanping, Cui Wen, Li Yijing
Department of Preventive Veterinary Medicine, College of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, Heilongjiang, People's Republic of China.
Appl Microbiol Biotechnol. 2014 Oct;98(19):8301-12. doi: 10.1007/s00253-014-5893-2. Epub 2014 Jul 4.
The role of muramyl dipeptide (MDP) and tuftsin in oral immune adjustment remains unclear, particularly in a Lactobacillus casei (L. casei) vaccine. To address this, we investigated the effects of different repetitive peptides expressed by L. casei, specifically the MDP and tuftsin fusion protein (MT) repeated 20 and 40 times (20MT and 40MT), in mice also expressing the D antigenic site of the spike (S) protein of transmissible gastroenteritis virus (TGEV) on intestinal and systemic immune responses and confirmed the immunoregulation of these peptides. Treatment of mice with a different vaccine consisting of L. casei expressing MDP and tuftsin stimulated humoral and cellular immune responses. Both 20MT and 40MT induced an increase in IgG and IgA levels against TGEV, as determined using enzyme-linked immunosorbent assay. Increased IgG and IgA resulted in the activation of TGEV-neutralising antibody activity in vitro. In addition, 20MT and 40MT stimulated the differentiation of innate immune cells, including T helper cell subclasses and regulatory T (Treg) cells, which induced robust T helper type 1 and T helper type 17 (Th17) responses and reduced Treg T cell immune responses in the 20MT and 40MT groups, respectively. Notably, treatment of mice with L. casei expressing 20MT and 40MT enhanced the anti-TGEV antibody immune responses of both the humoral and mucosal immune systems. These findings suggest that L. casei expressing MDP and tuftsin possesses substantial immunopotentiating properties, as it can induce humoral and T cell-mediated immune responses upon oral administration, and it may be useful in oral vaccines against TGEV challenge.
胞壁酰二肽(MDP)和促吞噬素在口服免疫调节中的作用仍不清楚,尤其是在干酪乳杆菌疫苗中。为了解决这个问题,我们研究了干酪乳杆菌表达的不同重复肽,特别是重复20次和40次的MDP和促吞噬素融合蛋白(MT)(20MT和40MT),对同样表达传染性胃肠炎病毒(TGEV)刺突(S)蛋白D抗原位点的小鼠肠道和全身免疫反应的影响,并证实了这些肽的免疫调节作用。用表达MDP和促吞噬素的干酪乳杆菌组成的不同疫苗治疗小鼠,刺激了体液免疫和细胞免疫反应。使用酶联免疫吸附测定法测定,20MT和40MT均诱导了针对TGEV的IgG和IgA水平升高。IgG和IgA的增加导致体外TGEV中和抗体活性的激活。此外,20MT和40MT刺激了先天免疫细胞的分化,包括辅助性T细胞亚类和调节性T(Treg)细胞,分别在20MT和40MT组中诱导了强大的1型辅助性T细胞和17型辅助性T细胞(Th17)反应,并降低了Treg T细胞免疫反应。值得注意的是,用表达20MT和40MT的干酪乳杆菌治疗小鼠增强了体液和黏膜免疫系统的抗TGEV抗体免疫反应。这些发现表明,表达MDP和促吞噬素的干酪乳杆菌具有显著的免疫增强特性,因为它在口服给药后可诱导体液免疫和T细胞介导的免疫反应,并且可能对抵抗TGEV攻击的口服疫苗有用。