| Literature DB >> 33287313 |
Zhengqing Yu1, Tianyuan Zhou1, Yanxin Luo1, Lu Dong1, Chunjing Li1, Junlong Liu2, Jianxun Luo2, Ruofeng Yan1, Lixin Xu1, Xiaokai Song1, Xiangrui Li1.
Abstract
Toxoplasma gondii (T. gondii) is the most common zoonotic protozoa and has infected about one-third of the population worldwide. Recombinant epitopes encapsulated in nanospheres have advantages over traditional T. gondii vaccines. For an efficient delivery system, poly (DL-lactide-co-glycolide) (PLGA) and chitosan are the most frequently used biodegradable polymeric nanospheres with strong safety profiles. In the present study, we first expressed and purified histone H2A1 of T. gondii using the prokaryotic expression system. The effects of recombinant TgH2A1 on the functions of murine macrophages were then studied. Purified recombinant TgH2A1 was then encapsulated in nanospheres with PLGA and chitosan. After subcutaneous vaccination in mice, the immune response was evaluated by double antibody sandwich ELISA kits. The results from this study showed that PLGA and chitosan loaded with rTgH2A1 could trigger a stronger Th1 oriented immune response and prolong the survival time of mice effectively. In conclusion, PLGA and chitosan nanospheres loaded with histone H2A1 are an effective method for the development of vaccines against T. gondii. Further studies should focus on evaluating the regulatory mechanism of TgH2A1, vaccine potency, and cellular response in chronic T. gondii infections.Entities:
Keywords: H2A1; PLGA; Toxoplasma gondii; chitosan; immune response; murine macrophage; nanoparticles
Year: 2020 PMID: 33287313 DOI: 10.3390/vaccines8040731
Source DB: PubMed Journal: Vaccines (Basel) ISSN: 2076-393X