Key result
Formalin inactivation of the CVB1 vaccine increased thermal stability and induced higher levels of protective neutralizing and IgG1 antibodies in mice compared to UV inactivation.
Why the study?
Type B Coxsackieviruses cause serious conditions like myocarditis and are vaccine targets, but previous 12-day formalin inactivation caused capsid disintegration and reduced virus concentration.
Does formalin inactivation improve the stability and immunogenicity of a Coxsackievirus B1 vaccine compared to UV inactivation in mice?
Does formalin inactivation improve the stability and immunogenicity of a Coxsackievirus B1 vaccine compared to UV inactivation in mice?
An optimized 5-day formalin inactivation method preserves Coxsackievirus B1 capsid structure and enhances immunogenicity compared to UV inactivation, making it a promising candidate for human clinical trials.
Answers are grounded in this paper and cite their sources.
Supports formalin over UV for CVB1 vaccine development; leaves open human translation.
Type B Coxsackieviruses (CVBs) belong to the enterovirus genus, and they cause both acute and chronic diseases in humans. CVB infections usually lead to flu-like symptoms but can also result in more serious diseases such as myocarditis, aseptic meningitis and life-threatening multi-organ infections in young infants. Thus, CVBs have long been considered as important targets of future vaccines. We have previously observed CVB1 capsid disintegration and virus concentration decrease with 12-day long formalin inactivation protocol. Here a scalable ion exchange chromatography purification method was developed, and purified CVB1 was inactivated with UV-C or formalin. Virus morphology and concentration remained unchanged, when the UV (2 min) or formalin (5 days) inactivation were performed in the presence of tween80 detergent. The concentration of the native and UV inactivated CVB1 remained constant at 4 °C during a six months stability study, whereas the concentration of the formalin inactivated vaccine decreased 29% during this time. UV treatment decreased, whereas formalin treatment increased the thermal stability of the capsid. The formalin inactivated CVB1 vaccine was more immunogenic than the UV inactivated vaccine; the protective neutralizing antibody levels were higher in mice immunized with formalin inactivated vaccine. High levels of CVB1 neutralizing antibodies as well as IgG1 antibodies were detected in mice that were protected against viremia induced by experimental CVB1 infection. In conclusion, this study describes a scalable ion exchange chromatography purification method and optimized 5-day long formalin inactivation method that preserves CVB1 capsid structure and immunogenicity. Formalin treatment stabilizes the virus particle at elevated temperatures, and the formalin inactivated vaccine induces high levels of serum IgG1 antibodies (Th2 type response) and protective levels of neutralizing antibodies. Formalin inactivated CVB vaccines are promising candidates for human clinical trials.
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Hankaniemi et al. (2019) studied Coxsackievirus B1 infection. Formalin inactivated CVB1 vaccine vs. UV inactivated CVB1 vaccine was evaluated on Stability and immunogenicity (neutralizing antibody levels and protection against viremia). Formalin inactivation of the CVB1 vaccine increased thermal stability and induced higher levels of protective neutralizing and IgG1 antibodies in mice compared to UV inactivation.
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