Comprehensive characterisation of shared immune mechanisms in organ-specific checkpoint induced and spontaneous autoinflammation
- Collaborators: Ben Fairfax, Fiona Powrie, Holm Uhlig, Simon Leedham
- Challenge: Minimising immuno-oncology toxicity
By enabling the collection of directly comparable datasets from multiple disease-specific sample collections, Oxford Cancer is extending multi-omic analysis of tissue and the microbiome from checkpoint inhibitor-treated patients with those with colitis. Oxford researchers are undertaking cross-tissue comparisons of immune related adverse events in collaboration with the CARTOGRAPHY consortium that will carry out single cell and microbiome mapping of inflammatory diseases in the gut, joints, liver and skin in partnership with Janssen Pharmaceuticals. In collaboration with national partners we will establish a national dataset with germline sequencing of patients that experience toxicity to identify risk factors to incorporate into the immune-therapy care pathway. When interpreted in the context of known immune mechanisms, germline risk factors could also indicate early (or prophylactic) deployment of adjunct therapies.