Studying Hepatitis Virus-Host Interactions in Patient Liver Biopsies
Overview
Affiliations
Infectious diseases are a major contributor to human suffering and the associated socioeconomic burden worldwide. A better understanding of human pathogen-host interactions is a prerequisite for the development of treatment strategies aimed at combatting human pathogen-induced diseases. Model systems that faithfully recapitulate the pathogen-host interactions in humans are critical to gain meaningful insight. Unfortunately, such model systems are not yet available for a number of pathogens. The strict tropism of the hepatitis B (HBV) and C (HCV) viruses for the human liver has made it difficult to study their virus-host interactions during the natural history of these infections. In this case, surplus liver biopsy tissue donated by patients provides an opportunity to obtain a snapshot of the phenomenological and molecular aspects of the human liver of chronically HCV or HBV-infected patients. In this review, we will briefly summarize our own efforts over the years to advance our knowledge of the virus-host interactions during the natural history of chronic HCV and HBV infection.
Tripartite Motif-Containing Protein 65 (TRIM65) Inhibits Hepatitis B Virus Transcription.
Shen S, Yan R, Xie Z, Yu X, Liang H, You Q Viruses. 2024; 16(6).
PMID: 38932182 PMC: 11209081. DOI: 10.3390/v16060890.
Ng E, Dobrica M, Harris J, Wu Y, Tsukuda S, Wing P J Gen Virol. 2023; 104(5).
PMID: 37196057 PMC: 10845048. DOI: 10.1099/jgv.0.001856.
Studying T Cell Responses to Hepatotropic Viruses in the Liver Microenvironment.
Lopez-Scarim J, Nambiar S, Billerbeck E Vaccines (Basel). 2023; 11(3).
PMID: 36992265 PMC: 10056334. DOI: 10.3390/vaccines11030681.