This review compares animal models of hepatitis A, highlighting their clinical features and implications for future research.
mice model was established with a specific mouse-adapted strain, recapitulating key clinical features of human hepatitis A. Recently, to overcome limitations associated with the difficulty in obtaining and amplifying stocks of HAV for animal models, our laboratory established a novel hepatitis A mouse model using lipid nanoparticle-encapsulated viral genomic RNA (LNP-vRNA). This approach provides a new strategy for modeling infections of hard-to-culture RNA viruses. In this review, we systematically summarize and compare these mouse models, respectively highlighting their advantages and limitations, and offer guidance for their application in future HAV research.
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