Dr David J Morgan

B.Sc.(Bristol), Ph.D.(Warw.)

  • BS8 1TD


Research output per year

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Personal profile

Research interests

Our laboratory is interested in examining the consequences of CD8+ T cell interactions with antigens expressed by normal tissues and cancers.  Earlier studies showed that priming of naive CD8+ T cells to become either effector CTL, or to be rendered tolerant is determined by a combination of signals mediated by professional antigen-presenting cells such as dendritic cells (DC) as well as normal and tumour cells.

We also know that altering any one of these signals dramatically shifts the balance between immune reactivity and tolerance induction.  The following projects aim to develop a deeper understanding of the cellular and molecular mechanisms that control T cell immunity to normal, infected and cancerous tissues:

  • To define the factors associated with both CD8+ T cells and tumor cells which influence the generation of effective anti-tumour responses.
  • To examine the role of the tumour microenvironment in controlling anti-tumour CD8+ T cell responses.
  • Development of novel vaccine approaches to combat human tumours.
  • Differential regulation of chronic inflammation in autoimmune disease.
  • To examine the role of dendritic cells (DC) during CD8+ T cell tolerence induction and autoimmunity to pancreatic self-antigens expressed by pancreatic islet β cell.

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Research Output

  • 18 Article (Academic Journal)

A Modular Vaccine Platform Combining Self‐Assembled Peptide Cages and Immunogenic Peptides

Morris, C., Glennie, S., Lam, H., Baum, H., Kandage, D., Williams, N., Morgan, D., Woolfson, D. & Davidson, A., 21 Feb 2019, In : Advanced Functional Materials. 29, 8, 12 p., 1807357.

Research output: Contribution to journalArticle (Academic Journal)

Open Access
  • 7 Citations (Scopus)
    106 Downloads (Pure)

    PD-1 suppresses the maintenance of cell couples between cytotoxic T cells and tumor target cells within the tumor

    Ambler, R., Edmunds, G., Morgan, D. & Wuelfing, C., 25 Apr 2019, (Submitted) In : Science Signaling.

    Research output: Contribution to journalArticle (Academic Journal)

  • ICAM-1 overexpression counteracts immune-suppress cell-derived PGE2 to restore CTL function

    Basingab, F. & Morgan, D., 6 Feb 2018, In : Journal of Immunological Sciences. 2, 1, p. 37-45 9 p.

    Research output: Contribution to journalArticle (Academic Journal)

    Open Access
  • 140 Downloads (Pure)

    Supervised Work

    High-throughput proteomic analysis of the dengue virus secretome and the identification of plasma biomarkers of disease severity

    Author: Luvira, V., 23 Jan 2020

    Supervisor: Morgan, D. (Supervisor) & Davidson, A. (Supervisor)

    Student thesis: Doctoral ThesisDoctor of Philosophy (PhD)

    Interaction between immune cells phenotype and the microbiome in B cells immunodeficiency diseases: miRNA & microbiomes in PIDDs

    Author: Al-Nesf Al-Mansouri, M. A. A. Y., 28 Nov 2019

    Supervisor: Morgan, D. J. (Supervisor) & Kafienah, W. (Supervisor)

    Student thesis: Master's ThesisMaster of Science (MSc)

    Interactions between CD8+ T cells and bone marrow-derived dendritic cells

    Author: Raveney, B. J. E., 2006

    Supervisor: Morgan, D. (Supervisor)

    Student thesis: Doctoral ThesisDoctor of Philosophy (PhD)