Dr Gareth Purvis

Retained Lecturer

I am a basic scientist by training with an in interest in innate immune cell biology primarily in cardiovascular disease.

I received my BSc (Hons) in Biology from the University of York where I received the Head of Departments award, before being accepted onto a 4 year MRes/PhD program funded by the British Heart Foundation at the William Harvey Research Institute, Queen Mary University of London.

Following completion of his PhD, entitled ‘Exploring the role of Annexin-A1 in the Pathophysiology of Diabetes Mellitus’, I moved to the University of Oxford where I work in the lab of Prof David Greaves within the Dunn School of Pathology and Prof Keith Channon in Cardiovascular medicine.

My main research focus is to understand at a single cell level how white blood cells called monocytes are recruited and re-programmed to undergo monocyte to macrophage differentiation at sites of inflammation. With a particular interest on how we can therapeutically alter this process to promote resolution of inflammation and tissue repair.

Dr Gareth Purvis

Retained Lecturer

I am a basic scientist by training with an in interest in innate immune cell biology primarily in cardiovascular disease.

I received my BSc (Hons) in Biology from the University of York where I received the Head of Departments award, before being accepted onto a 4 year MRes/PhD program funded by the British Heart Foundation at the William Harvey Research Institute, Queen Mary University of London.

Following completion of his PhD, entitled ‘Exploring the role of Annexin-A1 in the Pathophysiology of Diabetes Mellitus’, I moved to the University of Oxford where I work in the lab of Prof David Greaves within the Dunn School of Pathology and Prof Keith Channon in Cardiovascular medicine.

My main research focus is to understand at a single cell level how white blood cells called monocytes are recruited and re-programmed to undergo monocyte to macrophage differentiation at sites of inflammation. With a particular interest on how we can therapeutically alter this process to promote resolution of inflammation and tissue repair.