
Although hepatitis A virus (HAV) and hepatitis E virus (HEV) are both positive-strand RNA viruses that replicate in the cytoplasm of hepatocytes, there are important differences in the ways they induce and counteract host innate immune responses. HAV is remarkably stealthy because of its ability to evade and disrupt innate signaling pathways that lead to interferon production. In contrast, HEV does not block interferon production. Instead, it persists in the presence of an interferon response. These differences may provide insight into HEV persistence in immunocompromised patients, an emerging health problem in developed countries.
Inflammasomes, Hepatitis A, Immunity, Innate, Hepatitis E, Disease Models, Animal, Liver, Drug Resistance, Viral, Hepatitis E virus, Hepatocytes, Animals, Humans, Hepatitis A virus, Interferons, Cells, Cultured
Inflammasomes, Hepatitis A, Immunity, Innate, Hepatitis E, Disease Models, Animal, Liver, Drug Resistance, Viral, Hepatitis E virus, Hepatocytes, Animals, Humans, Hepatitis A virus, Interferons, Cells, Cultured
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 22 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
