Theme 2: Intrahepatic Hepatitis B &
Theme 2.2: Identifying and characterising intrahepatic immune cells in CHB

Dr John Connolly
Research Director of Translational Immunology Programme
Head of Section on Immuno-oncology and Cell Therapy at the Institute of Molecular and Cell Biology (IMCB), A*STAR

Dr John Connolly is the theme leader for theme 2 of the LCG (Intrahepatic Hepatitis B) and heads the section on “Identifying and characterizing intrahepatic immune cells in CHB”.  Dr Connolly has vast experience in human immunology and is focused in studying immune modulation during chronic viral infection and therapy. His other research interests are immunotherapy and immune-metabolism.

This theme focuses on a comprehensive evaluation of intrahepatic biology from the same CHB phenotypically identified patients from theme 1 (n=250), through liver biopsy (IRB approval 2000/00828 for 4 liver cores per patient), thus take a unique multi-dimensional approach to understanding intrahepatic events. Liver biopsy assignment: core 1 – single cell analysis; core 2 – proteomics/immune cell isolation; core 3 – HBV virology; core 4 – routine processing for histology report. 

 

 

 

Theme 2.1: Unravelling HBV-induced changes to the host transcriptome/epigenome by single cell analysis

Dr Ramanuj Dasgupta
Senior Group Leader, Precision Oncology, Genome Institute of Singapore (GIS)

In this theme, the liver cells and PBMCs will be used to implement an integrated approach of transcriptomic and chromatin accessibility analysis to evaluate the transcription profile, and functional gene regulatory networks that modulate the phenotypes of Hepatitis B.

 

 

 

Theme 2.3: Characterisation of hepatic proteome and chromatin state dysregulation associated with different CHB phenotypes

Dr Jayantha Gunaratne
Senior Principal Investigator, Institute of Molecular and Cell Biology, A*STAR
Associate Professor, Yong Yoo Lin, National University of Singapore

Dr Jayantha is the Co-Investigator responsible for proteomics-centric discovery of surrogate circulating protein markers for CHB, analysis of dysregulation of hepatic proteome/PTMs associated with different CHB phenotypes and characterizing previously identified novel drug targets.

 

 

 

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