Why the study?
Coxsackievirus B5 causes meningitis and hand, foot, and mouth disease and is linked to type 1 diabetes, but no effective drug or vaccine exists.
The KM299-L05 strain shows potential as a novel CVB5 vaccine candidate, providing full protection in a neonatal mouse model.
KM299-L05 vaccine merits further preclinical study; leaves open human efficacy and safety.
Objective: Evidence indicates that coxsackievirus B5 (CVB5) can cause meningitis, and hand, foot, and mouth disease (HFMD), and is associated with type 1 diabetes. No effective drug or vaccine is available for treating CVB5 infections or controlling outbreaks. Methods: The Vero-cell-adapted vaccine candidate strain KM299-L05 underwent comprehensive phylogenetic analysis, sequence alignment, assessment of virulence in BALB/c mice, Vero cell acclimation, three successive rounds of plaque purification, preparation of experimental vaccines, and immunogenicity evaluation. Results: KM299-L05 was the most virulent strain in BALB/c mice. Its infectious titer reached 10 8.0 CCID 50 /mL in Vero cells, and it belonged to the Chinese epidemic genotype C3. An inactivated CVB5 vaccine derived from the KM299-L05 strain produced neutralizing antibodies with a titer range from 1:384 to 1:768 against a variety of clinical CVB5 isolates, particularly the prototype strain. Maternal antibodies fully protected all examined suckling BALB/c mice against lethal challenge. Conclusion: Although the study was limited to neonatal mice, our findings suggested that the KM299-L05 strain has potential as a novel CVB5 vaccine candidate in China, and provide a rationale for the development of a CVB5 vaccine.
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Liu et al. (2025) studied this question.
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