Projects per year
The Wooldridge Clinical T cell lab group which is led by Professor Linda Wooldridge has three main areas of interest, these include;
1. CD8+ T cell mediated conditions such as autoimmunity and T cell leukaemia.
2. Targeting the CD8 co-receptor for therapeutic benefit.
CD8 has a potent ability to tune the antigen specific immune response. As such, we ae investigating the possiblity that targetting CD8 can be used to:
- Block the pathogenic CD8+ T cell attack observed in autoimmune disease and transplant rejection (Mathew Clement).
- Enhance CD8+ T cell immunity especially in a cancer setting where responses are suboptimal (Tamsin Williams).
Unique Recognition System
CD8+ T cells recognize antigenic determinants in the form of short peptides derived from endogenous peptides bound to MHC class I (pMHCI). CD8+ T cell recognition of pMHCI involves the binding of two receptors (T cell receptor; TCR and CD8) to a single ligand (pMHCI), a modus operandi that is unique to ab T cell biology. Therefore CD8+ T cell activation involves two key interactions:
- The TCR/pMHCI interaction: determines antigen specificity. Promiscuity is a characteristic feature of this interaction and it is essential for effective immunity.
- The pMHCI/CD8 interaction: has a potent ability to tune the antigen specific immune response by a number of different mechanisms.
Figure 1: Interaction between TCR MHCI and CD8
We are interested in understanding both of these interactions and how to manipulate them for therapeutic benefit.
3. Development of technology to study the TCR and CD8 co-receptor.
Our overall aim is to understand the mechanisms of CD8+ T-cell mediated disease and use this knowledge to develop novel therapeutic reagents.
Further information about Professor Linda Wooldridge can be found here.
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1/10/20 → 31/03/22
1/10/20 → 31/03/21
- 36 Article (Academic Journal)
Young infants exhibit robust functional antibody responses and restrained IFN-γ production to SARS-CoV-2Goenka, A., Halliday, A., Gregorova, M., Milodowski, E. J., Thomas, A., Kavanagh Williamson, M., Baum, H. E., Oliver, E. H., Long, A. E., Knezevic, L., Gupta, K., Di Bartolo, N. D., Berger, I., Toye, A. M., Bernatoniene, J., Bailey, M., Gillespie, K. M., Davidson, A. D., Wooldridge, L., Rivino, L. & 1 others, , 20 Jul 2021, In: Cell Reports Medicine. 2, 7, 13 p., 100327.
Research output: Contribution to journal › Article (Academic Journal) › peer-reviewOpen AccessFile2 Citations (Scopus)13 Downloads (Pure)
Whalley, T., Dolton, G., Brown, P. E., Wall, A., Wooldridge, L., van den Burg, H., Fuller, A., Hopkins, J. R., Crowther, M. D., Attaf, M., Knight, R. R., Cole, D. K., Peakman, M., Sewell, A. K. & Szomolay, B., 28 Feb 2020, In: Frontiers in Immunology. 11, 18 p., 296.
Research output: Contribution to journal › Article (Academic Journal) › peer-reviewOpen AccessFile62 Downloads (Pure)
Post-acute COVID-19 associated with evidence of bystander T-cell activation and a recurring AMR bacterial pneumoniaGregorova, M., Morse, D., Brignoli, T., Steventon, J., Hamilton, F., Albur, M., Arnold, D., Thomas, M., Halliday, A., Baum, H., Rice, C., Avison, M. B., Davidson, A. D., Santopaolo, M., Oliver, E., Goenka, A., Finn, A., Wooldridge, L., Amulic, B., Boyton, R. J. & 10 others, , 17 Dec 2020, (E-pub ahead of print) In: eLife. 9, 13 p., e63430.
Research output: Contribution to journal › Article (Academic Journal) › peer-reviewOpen AccessFile16 Downloads (Pure)