| Literature DB >> 26852892 |
A Gisa1, P V Suneetha1, P Behrendt1, S Pischke1,2, B Bremer1, C S Falk3, M P Manns1, M Cornberg1,4, H Wedemeyer1,4, A R M Kraft1.
Abstract
Hepatitis E is an inflammatory liver disease caused by infection with the hepatitis E virus (HEV). In tropical regions, HEV is highly endemic and predominantly mediated by HEV genotypes 1 and 2 with >3 million symptomatic cases per year and around 70 000 deaths. In Europe and America, the zoonotic HEV genotypes 3 and 4 have been reported with continues increasing new infections per year. So far, little is known about T-cell responses during acute HEV genotype 3 infection. Therefore, we did a comprehensive study investigating HEV-specific T-cell responses using genotypes 3- and 1-specific overlapping peptides. Additional cytokines and chemokines were measured in the plasma. In four patients, longitudinal studies were performed. Broad functional HEV-specific CD4(+) and CD8(+) T-cell responses were detectable in patients acutely infected with HEV genotype 3. Elevated of pro- and anti-inflammatory cytokine levels during acute HEV infection correlated with ALT levels. Memory HEV-specific T-cell responses were detectable up to >1.5 years upon infection. Importantly, cross-genotype HEV-specific T-cell responses (between genotypes 1 and 3) were measurable in all investigated patients. In conclusion, we could show for the first time HEV-specific T-cell responses during and after acute HEV genotype 3 infection. Our data of cross-genotype HEV-specific T-cell responses might suggest a potential role in cross-genotype-specific protection between HEV genotypes 1 and 3.Entities:
Keywords: T cell; cellular immune response; cross-genotype; hepatitis; hepatitis E virus (HEV)
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Year: 2016 PMID: 26852892 DOI: 10.1111/jvh.12495
Source DB: PubMed Journal: J Viral Hepat ISSN: 1352-0504 Impact factor: 3.728