Sustained drug-free remission (SDFR) is achievable in up to 50% of patients with rheumatoid arthritis (RA) in drug-induced remission. However, methods to predict SDFR, its immunological basis, and its impact from a patient perspective remain unknown. The goal of this proposal is to address these unmet needs in three distinct yet complementary work packages (WPs). In WP1, we aim to validate our prototype cytokine biomarker of SDFR using our existing sample biobanks. In WP2, we aim to explore and understand specific mechanisms that potentiate SDFR as implicated by our pilot data, namely: the abundance, phenotype and function of CD4+ regulatory T cells (Tregs) and ACPA-expressing B cell subsets; and markers of regulatory macrophage and intestinal barrier function. In WP3, we aim to understand the impact of living with SDFR from a patient perspective using qualitative methodology. If successful, our project will support a future clinical efficacy trial of biomarker-driven drug cessation in RA remission, a paradigm shift in the management of RA. Furthermore, new insights into the immunobiology of SDFR could identify novel approaches to treat and prevent RA flare, and understanding the lived experience of SDFR will help to guide patient-clinician discussions around drug cessation.
Patient research partners form an integral component of this project, and cut across all proposed activities. Our patient research partners will: