Professor Mark Vickers

Professor Mark Vickers
Professor Mark Vickers
Professor Mark Vickers

MBChB MRCP DM FRCPath

Chair in Applied Medicine (Clin)

About
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

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

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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  • Evidence for a quantitative trait locus for plasma fibrinogen from a family-based association study.

    Mayosi, B. M., Vickers, M. A., Green, F. R., Ratcliffe, P. J., Julier, C., Lathrop, G. M., Watkins, H., Keavney, B.
    Genescreen, vol. 1, pp. 151-155
    Contributions to Journals: Articles
  • In vivo platelet activation in atherothrombotic stroke is not determined by polymorphisms of human platelet glycoprotein IIIa or Ib

    Meiklejohn, D. J., Vickers, M. A., Morrison, E. R., Dijkhuisen, R., Moore, I., Urbaniak, S., Greaves, M.
    British Journal of Haematology, vol. 112, no. 3, pp. 621-631
    Contributions to Journals: Articles
  • Monosomy for the most telomeric, gene-rich region of human chromosome 16p causes minimal phenotypic effects

    Horsley, S. W., Daniels, R. J., Anguita, E., Raynham, H. A., Peden, J. F., Villegas, A., Vickers, M. A.
    EJHG : European journal of human genetics : the official journal of the European Society of Human Genetics. , vol. 9, pp. 217-225
    Contributions to Journals: Articles
  • Beta-tubulin gene mutations and response to vinca alkaloids in acute lymphoblastic leukaemia

    Milner, B. J., Vickers, M. A., Schofield, A. C., Culligan, D. J., Tighe, J. E., Haites, N. E., King, D.
    Journal of Medical Genetics, vol. 37, no. Supplement, pp. S42
    Contributions to Journals: Articles
  • Genetic basis of variation in fibrinogen and CRP

    Mayosi, B. M., Green, F. R., Vickers, M. A., Watkins, H., Keavney, B.
    Heart, vol. 83, no. SUPPL. 1
    Contributions to Journals: Articles
  • Modelling haemopoietic stem cell division by analysis of mutant red cells

    Vickers, M., Brown, G. C., Cologne, J. B., Kyoizumi, S.
    British Journal of Haematology, vol. 110, pp. 54-62
    Contributions to Journals: Articles
  • The incidence of acute promyelocytic leukemia appears constant over most of a human lifespan, implying only one rate limiting mutation

    Vickers, M., Jackson, G., Taylor, P.
    Leukemia, vol. 14, pp. 722-726
    Contributions to Journals: Articles
  • Splenic irradiation before bone marrow transplantation for chronic myeloid leukaemia (multiple letters) [9]

    Vickers, M., Gratwohl, A., Hermans, J.
    British Journal of Haematology, vol. 97, no. 1, pp. 248-249
    Contributions to Journals: Letters
  • More or less hematopoietic stem cells

    Vickers, M.
    Nature Medicine, vol. 2, no. 12, pp. 1281-1282
    Contributions to Journals: Letters
  • Estimation of the number of mutations necessary to cause chronic myeloid leukaemia from epidemiological data

    Vickers, M.
    Contributions to Journals: Short Survey
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