Immunology

How do antimicrobial peptides alter T cell cytokine production?

University of Southampton

Not stated

Location
Southampton, United Kingdom
Funding
Fully funded (UK only); £17,688 tax-free each year
Application deadline
See university guidance

About the project

This project will use a variety of immunology, molecular biology and data-driven approaches to work out how antimicrobial peptides affect T cell function, and what this means for disease.

Antimicrobial peptides are released by neutrophils, mast cells and epithelial cells during infectious and inflammatory disease. They have many effects on innate and adaptive immune cells. We have recently shown that one antimicrobial peptide in particular, cathelicidin, drives differentiation of the Th17 subset of T cells ( Minns Nature Communications 2021 ). We have also shown that this peptide-induced T cell differentiation causes autoimmune disease in a model of Multiple Sclerosis ( Smith PLOS Biology 2022 ). This is exciting because it has shown that these ubiquitous peptides may have far greater impact on adaptive immunity than we had previously imagined.

Now, we want to investigate this process in much greater depth. We know that cathelicidin gets into T cells and alters cytokine expression – particularly IL-17F and IFN-γ. We do not know how this occurs or which signalling pathways are involved. In this project we will use a variety of techniques to decipher how peptide exposure alters the pathways leading to production of these cytokines. We will work out what this means for a number of models of disease – including autoimmune, infection and cancer models.

The student will use techniques including multi-colour and spectral flow cytometry, confocal microscopy, ELISA, isolation and culture of T cells and analysis of RNA sequencing data. Animal handling and in vivo models of disease will be involved in the project. They will be fully trained in all these techniques as well as in statistics, coding, presentation skills, writing skills, and data management.

Lead supervisor

  • Lead supervisor: Professor Emily Gwyer Findlay MSci PhD FHEA Professor

Professor Emily Gwyer Findlay MSci PhD FHEA

  • Professor Emily Gwyer Findlay MSci PhD FHEA: Professor

Professor Edd James

  • Antigen processing and presentation
  • Regulation of T cell responses in anti-tumour responses

Entry requirements

You'll need:

We encourage students from a diverse range of disciplines to apply.

This studentship is only available for home students.

  • a UK 2:1 honours degree
  • an interest in immunology

Fees and funding

For UK students, tuition fees and a stipend of £17,688 tax-free each year for up to 3.5 years.

How to apply

Apply now by email

You need to include:

  • your cv (resumé)
  • degree transcripts to date
  • 2 references
  • a cover letter stating why you are interested in this PhD

Faculty of environmental and life sciences

Email: fels-gradschool@soton.ac.uk

Project leader

If you wish to discuss any details of the project informally, please contact Dr Emily Gwyer Findlay.

Email: E.Gwyerfindlay@soton.ac.uk

Research areas

ImmunologyMicrobiology

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