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Updated: Sep 10, 2025

Using Reverse Genetics to Manipulate the NSs Gene of the Rift Valley Fever Virus MP-12 Strain to Improve Vaccine Safety and Efficacy
Published on: November 1, 2011
The mRNA vaccine encoding Gc protein confers complete protection against severe fever with thrombocytopaenia syndrome
Xiaoyu Zhang1, Xuekai Zhang1, Jing Lu2
1State Key Laboratory of Virology and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, China; Center for Biosafety Mega-Science, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, China; University of Chinese Academy of Sciences, Beijing, China.
Abstract:
Severe fever with thrombocytopaenia syndrome virus (SFTSV), an emerging tick-borne pathogen, causes haemorrhagic fever in infected patients and is associated with a high mortality rate in humans. The imperative need for vaccines against this lethal virus is underscored by a lack of effective preventive measures. The results of this study yield notable advancements: the successful development of an SFTSV mRNA vaccine encoding the glycoprotein C (Gc) gene, achieving N-linked glycosylation in the expressed protein. This vaccination regimen induced a balanced TH1/TH2 immune response and elicited robust levels of both cellular and humoral immunity in C57BL/6 and IFNAR-/- mice. The results of the present study demonstrate that immunization with 1 μg mRNA vaccine provides complete protection (100 %) against lethal SFTSV infection (77,000 LD50) in IFNAR-/- mice. Moreover, the vaccine candidate induces long-lasting immunity and confers protection against SFTSV for at least six months. Notably, the antibody provides 100 % protection according to passive transfer assays, suggesting that humoral immunity plays a crucial role in resisting SFTSV challenge. These findings present a promising stride forward in the quest for an effective vaccine against SFTSV, highlighting the potential of the developed mRNA vaccine in conferring substantial immunity.
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