MBChB MRCP DM FRCPath
Chair in Applied Medicine (Clin)
- About
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- Email Address
- m.a.vickers@abdn.ac.uk
- Telephone Number
- +44 (0)1224 272401
- Office Address
1. Room 3:25, Institute of Medical Sciences
2. Blood Transfusion Centre, Foresterhill Road, Aberdeen AB25 2ZW
- School/Department
- School of Medicine, Medical Sciences and Nutrition
Biography
I graduated from Oxford Medical School in 1983, having completed a Biochemistry Part II at Cambridge. After general medical jobs in London, I worked with Doug Higgs on genes surrounding the alpha-globin gene cluster. I then trained in clinical Haematology at the Hammersmith, Reading and John Radcliffe Hospitals (1990–1996). I moved to Aberdeen in 1996 and was promoted to Professor in the section of Applied Medicine in 2008. I took over directorship of the Academic Transfusion Medicine Unit in 2010.
External Memberships
Member of Royal College of Physicians
Fellow of Royal College of Pathologists
British Society for Haematology
- Research
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Research Overview
My main current interest is in how cells are recognised as being damaged by phagocytes, using red blood cells as the main model system. Our work has implicated unusual glycosylation motifs as being key to the process and are of particular relevance to the mechanism of haemolysis in sickle cell disease and malaria. The mechanism gives insight into splenic function, notably susceptibility to pneumococcal infection. I have interests in cellular immunotherapy, including the use of blood donor derived cytotoxic lymphocytes to treat post-transplant lympoproliferative disease and COVID-19. I am supervising PhD students developing innate immunotherapeutic reagents to treat cancers. I am also involved in collection and use of convalescent plasma for COVID-19.My main current interest is in how cells are recognised as being damaged by phagocytes, using red blood cells as the main model system. Our work has implicated unusual glycosylation motifs as being key to the process and are of particular relevance to the mechanism of haemolysis in sickle cell disease and malaria. The mechanism gives insight into splenic function, notably susceptibility to pneumococcal infection. I have interests in cellular immunotherapy, including the use of blood donor derived cytotoxic lymphocytes to treat post-transplant lympoproliferative disease and COVID-19. I am supervising PhD students developing innate immunotherapeutic reagents to treat cancers. I am also involved in collection and use of convalescent plasma for COVID-19.
Knowledge Exchange
I have given talks about the use of convalescent plasma and T cells to treat COVID-19.
Collaborations
Prof. Alex Rowe, Edinburgh University.
Prof. Stuart Haslam, Imperial College London.
Prof. David Rees, King's College London.
Supervision
Shiva Nickaria, Raquel Ferro, Ellen Main - all working on immunotherapies.
- Teaching
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Teaching Responsibilities
I organise, and deliver much of, the haematology training in the medical school. I remain an enthusiastic bedside teacher. I co-ordinated the third year medical degree 1997-2010.
- Publications
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Page 9 of 9 Results 81 to 90 of 90
Evidence for a quantitative trait locus for plasma fibrinogen from a family-based association study.
Genescreen, vol. 1, pp. 151-155Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1046/j.1466-920x.2001.00037.x
In vivo platelet activation in atherothrombotic stroke is not determined by polymorphisms of human platelet glycoprotein IIIa or Ib
British Journal of Haematology, vol. 112, no. 3, pp. 621-631Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1046/j.1365-2141.2001.02620.x
Monosomy for the most telomeric, gene-rich region of human chromosome 16p causes minimal phenotypic effects
EJHG : European journal of human genetics : the official journal of the European Society of Human Genetics. , vol. 9, pp. 217-225Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1038/sj.ejhg.5200610
Beta-tubulin gene mutations and response to vinca alkaloids in acute lymphoblastic leukaemia
Journal of Medical Genetics, vol. 37, no. Supplement, pp. S42Contributions to Journals: ArticlesGenetic basis of variation in fibrinogen and CRP
Heart, vol. 83, no. SUPPL. 1Contributions to Journals: Articles- [ONLINE] View publication in Scopus
Modelling haemopoietic stem cell division by analysis of mutant red cells
British Journal of Haematology, vol. 110, pp. 54-62Contributions to Journals: ArticlesThe incidence of acute promyelocytic leukemia appears constant over most of a human lifespan, implying only one rate limiting mutation
Leukemia, vol. 14, pp. 722-726Contributions to Journals: ArticlesSplenic irradiation before bone marrow transplantation for chronic myeloid leukaemia (multiple letters) [9]
British Journal of Haematology, vol. 97, no. 1, pp. 248-249Contributions to Journals: Letters- [ONLINE] View publication in Scopus
More or less hematopoietic stem cells
Nature Medicine, vol. 2, no. 12, pp. 1281-1282Contributions to Journals: Letters- [ONLINE] DOI: https://doi.org/10.1038/nm1296-1281b
- [ONLINE] View publication in Scopus
Estimation of the number of mutations necessary to cause chronic myeloid leukaemia from epidemiological data
Contributions to Journals: Short Survey- [ONLINE] DOI: https://doi.org/10.1046/j.1365-2141.1996.d01-1751.x
- [ONLINE] View publication in Scopus