EMITTIC: The Enteric Microbiome as a Therapeutic Target in Cirrhosis

  • Research type

    Research Study

  • Full title

    The faecal microbiome as a therapeutic target for restoring unconventional T cell immunity in cirrhosis

  • IRAS ID

    255103

  • Contact name

    Debbie Shawcross

  • Contact email

    debbie.shawcross@kcl.ac.uk

  • Sponsor organisation

    King's College London

  • Duration of Study in the UK

    3 years, 0 months, 5 days

  • Research summary

    The proportions of ‘good’ and ‘bad’ bacteria in the gut are key to remaining healthy and become unbalanced in patients with chronic liver disease (CLD). This causes the gut to become more 'leaky' with bacteria escaping into the bloodstream, causing activation of the immune system which becomes exhausted and is then unable to fight infection. In patients with CLD, disruption of the immune system resulting in frequent bacterial infections; these infections are often severe, frequently resulting in hospitalisation and death despite best medical care. New treatments to restore immune function in cirrhosis are urgently needed.

    We hypothesise that recently described unconventional T cells (a population of immune cells) are key mediators of abnormal interactions between the gut bacteria and the host immune system in cirrhosis and that their functions can be modified by targeting the gut bacteria to restore a healthy balance. We aim to show the mechanisms by which gut bacteria control the function of key immune cell populations in CLD and to assess the role of targeted treatments to restore immune cell function.

    We propose an observational study of licensed therapies including b-blockers and rifaximin-α (a non-absorbable antibiotic licensed for end stage chronic liver disease with hepatic encephalopathy). We will collect participant blood, stool, saliva and urine before and after treatment. We will perform ‘state of the art’ analysis of the gut microbiome and its products of metabolism and better understand the imbalance of bacteria in the gut in CLD and its impact on host immune function. In undertaking this project we will combine a collaborative team of academic leaders in the fields of liver disease and immunology.

  • REC name

    East Midlands - Leicester South Research Ethics Committee

  • REC reference

    20/EM/0101

  • Date of REC Opinion

    3 Jun 2020

  • REC opinion

    Further Information Favourable Opinion