Stratified interventions in ARDS (EMINENT)
Lead Research Organisation:
University of Cambridge
Department Name: Medicine
Abstract
There is an urgent and unmet need to define disease pathogenesis in acute respiratory distress syndrome (ARDS), and to develop rapid diagnostics to aid patient stratification and support targeted intervention. This is a programmatic approach to define disease pathogenesis in ARDS, and to develop rapid diagnostics to aid patient stratification and support targeted intervention.
Technical Summary
WP1: ARDS: in whom to intervene? This will involve an unbiased informatics-based analysis of existing (HARP2, REST, MOSAIC, GALAXY, ARDS.NET) and new patient cohorts to define ARDS endotypes
WP2: ARDS: when to intervene? Undertake prospective analysis of trans-pulmonary cytokine, genomic/epigenomic and neutrophil and monocyte phenotyping/migration signatures, and novel imaging modalities (SPECT/CT, PET/CT) to define the optimal time for intervention in the above cohorts, and to develop rapid ('by lunchtime') diagnostic platforms. This WP will specifically test the concepts generated in well-established and highly refined animal, human lung slice and EVLP models of ALI
WP3: ARDS with what to intervene? The collaborative network established above will, together with GSK, be ideally positioned to deliver Phase IIa experimental POC studies, using existing assets in the specific subtypes identified; endpoints (e.g. vascular leak, cell migration, physiological indices, biomarkers) will be determined by the endotype under study
WP2: ARDS: when to intervene? Undertake prospective analysis of trans-pulmonary cytokine, genomic/epigenomic and neutrophil and monocyte phenotyping/migration signatures, and novel imaging modalities (SPECT/CT, PET/CT) to define the optimal time for intervention in the above cohorts, and to develop rapid ('by lunchtime') diagnostic platforms. This WP will specifically test the concepts generated in well-established and highly refined animal, human lung slice and EVLP models of ALI
WP3: ARDS with what to intervene? The collaborative network established above will, together with GSK, be ideally positioned to deliver Phase IIa experimental POC studies, using existing assets in the specific subtypes identified; endpoints (e.g. vascular leak, cell migration, physiological indices, biomarkers) will be determined by the endotype under study
Publications
Anthony Yong Kheng Cordero N
(2023)
Efficient Methods for Target Gene Manipulation in Haematopoietic Stem Cell Derived Human Neutrophils
Bos LDJ
(2021)
Precision medicine in acute respiratory distress syndrome: workshop report and recommendations for future research.
in European respiratory review : an official journal of the European Respiratory Society
Colzani M
(2024)
Proinflammatory cytokines driving cardiotoxicity in COVID-19.
in Cardiovascular research
Dunmore B
(2023)
Reduced circulating BMP9 and pBMP10 in hospitalized COVID-19 patients
in Pulmonary Circulation
Ekpenyong A
(2017)
Mechanical deformation induces depolarization of neutrophils
in Science Advances
Ganapathi S
(2022)
Tackling bias in AI health datasets through the STANDING Together initiative.
in Nature medicine
Iyadurai L
(2023)
Reducing intrusive memories after trauma via an imagery-competing task intervention in COVID-19 intensive care staff: a randomised controlled trial.
in Translational psychiatry
Mehta P
(2020)
Therapeutic blockade of granulocyte macrophage colony-stimulating factor in COVID-19-associated hyperinflammation: challenges and opportunities.
in The Lancet. Respiratory medicine
| Description | Stratified interventions in ARDS: EMINENT ARDS Work Package 2. |
| Amount | £952,329 (GBP) |
| Funding ID | MR/X005070/1 |
| Organisation | Medical Research Council (MRC) |
| Sector | Public |
| Country | United Kingdom |
| Start | 12/2022 |
| End | 11/2025 |
| Description | Collaboration with GlaxoSmithKline |
| Organisation | GlaxoSmithKline (GSK) |
| Department | Research and Development GSK |
| Country | United Kingdom |
| Sector | Private |
| PI Contribution | This programme grant is via the MRC-GSK EMINENT network. Alongside the programme is a GSK-NIHR BRC co-funded PhD clinical research training fellowship. |
| Collaborator Contribution | GSK have provided expertise, technical support, compounds, training and hosting of research team members. The research fellow has spent 6 months FTE embedded at GSK R&D. |
| Impact | Follow-on funding is pending. Publications about to be submitted, |
| Start Year | 2018 |
| Description | Rachel Chambers / UCL via EMINENT |
| Organisation | University College London |
| Country | United Kingdom |
| Sector | Academic/University |
| PI Contribution | Partner in EMINENT-ARDS programme. |
| Collaborator Contribution | Joint development/delivery of validation work stream for EMINET-ARDS programme, |
| Impact | None as yet. |
| Start Year | 2020 |
| Title | Otilimab clinical trial |
| Description | Based on work undertaken as part of EMINENT WP 1, Otilimab was progressed by GSK into Phase 3 clinical trial for COVID-19. |
| Type | Therapeutic Intervention - Drug |
| Current Stage Of Development | Late clinical evaluation |
| Year Development Stage Completed | 2022 |
| Development Status | On hold |
| Clinical Trial? | Yes |
| Impact | Otilimab was repurposed as a potential therapy for COVID-19 pneumonia based on findings from EMINENT-ARDS but was subsequently found not to be of benefit in a Phase 3 trial, in which I collaborated as the UK Chief Investigator. |