Key result
The EV71-VP1 protein vaccine elicited similar humoral and cellular immune responses compared to inactivated EV71, and vaccinated female mice conferred protection to their neonatal offspring.
Why the study?
Does EV71-VP1 protein induce effective immunologic protection against EV71 in mice?
Does EV71-VP1 protein induce effective immunologic protection against EV71 in mice?
EV71-VP1 protein induces effective immunologic protection against EV71 in mice, suggesting it is a promising, safer, and more economical vaccine candidate compared to inactivated EV71.
Answers are grounded in this paper and cite their sources.
May advance EV71 vaccine candidates; leaves open clinical efficacy trials.
Enterovirus 71 (EV71) is an important agent responsible for hand-foot-and-mouth disease (HFMD), which can cause severe neurological complications and death in children. However, there is no specific treatment for EV71 infection, and a safe and effective vaccine is needed urgently. In this study, an effective and economical method for the production of EV71-VP1 protein was developed, and the VP1 protein was evaluated in humoral and cellular immune responses as an EV71 vaccine. The results revealed that the VP1 protein induced high titers of cross-neutralizing antibodies for different EV71 subtypes, and elicited significant splenocyte proliferation. The high levels of IFN-r and IL-10 showed the VP1 protein induced a mixed Th1 and Th2 immune response. Vaccinated female mice could confer protection in their neonatal offspring. Compared with the inactivated EV71, the VP1 protein elicited similar humoral and cellular responses, but the engineered protein is safer, less expensive and can be produced more efficiently. Therefore, EV71-VP1 protein can induce effective immunologic protection against EV71 and is an ideal candidate against EV71 infection.
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Zhou et al. (2014) studied Enterovirus 71 (EV71) infection. EV71-VP1 protein vs. Inactivated EV71 was evaluated on Humoral and cellular immune responses and protection in neonatal offspring. The EV71-VP1 protein vaccine elicited similar humoral and cellular immune responses compared to inactivated EV71, and vaccinated female mice conferred protection to their neonatal offspring.
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