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Induction of Protective Immunity against Toxoplasma gondii in Mice by Nucleoside Triphosphate Hydrolase-II (NTPase-II) Self-amplifying RNA Vaccine Encapsulated in Lipid Nanoparticle (LNP)
被引:37
|作者:
Luo, Fangjun
[1
]
Zheng, Lina
[2
]
Hu, Yue
[3
]
Liu, Shuxian
[3
]
Wang, Yan
[3
]
Xiong, Zhongkui
[4
]
Hu, Xin
[5
,6
]
Tan, Feng
[3
]
机构:
[1] Zhuji Peoples Hosp, Dept Clin Lab, Zhuji, Peoples R China
[2] Wenzhou Med Univ, Inst Stem Cell & Tissue Engn, Sch & Hosp Stomatol, Wenzhou, Peoples R China
[3] Wenzhou Med Univ, Sch Basic Med Sci, Dept Parasitol, Wenzhou, Peoples R China
[4] Shaoxing Second Hosp, Dept Radiat Oncol, Shaoxing, Peoples R China
[5] Wenzhou Med Univ, Dept Basic Lab Med, Sch Med Lab Sci, Wenzhou, Peoples R China
[6] Wenzhou Med Univ, Sch Life Sci, Wenzhou, Peoples R China
关键词:
Toxoplasma gondii;
vaccine;
nucleoside triphosphate hydrolase;
self-amplifying RNA;
lipid nanoparticle (LNP);
MESSENGER-RNA;
IFN-GAMMA;
DIRECT-INJECTION;
DNA VACCINES;
IMMUNIZATION;
RESPONSES;
VIRUS;
ENCEPHALITIS;
EXPRESSION;
CHALLENGES;
D O I:
10.3389/fmicb.2017.00605
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
RNA-based vaccine represents an irresistible and safe immunization strategy with decreasing theoretical risks of genomic integration and malignant cell transformation. To our knowledge, however, there is no report about development of RNA vaccine against Toxoplasma gondii infection. We have previously demonstrated that the recombinant T. gondii nucleoside triphosphate hydrolase-II (NTPase-II) protein is able to provide protective Th1 cell-mediated immunity against T. gondii. Herein, we evaluated the immunogenic potential of a self-amplifying RNA vaccine-encoding T. gondii NTPaseII gene, RREP-NTPase-II, delivered by a synthetic lipid nanoparticle (LNP). Immunization of mice with naked RREP-NTPase-II induced a strong cellular and humoral immune response with high-IgG antibody titers and IFN-g production. The immunized mice displayed significantly prolonged survival time and reduction in brain parasite load (46.4%) compared with control group. Furthermore, mice vaccinated with RREPNTPase-II-encapsulated LNP displayed significantly enhanced protection against acute infection as well as chronic infection with PRU cyst, which shows 62.1% reduction in brain cyst burden in comparison to control group. These results suggest that the combination of self-amplifying RNA and LNP ion would be beneficial to the development of a safe and long-acting vaccine against toxoplasmosis.
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