Postgrad LIVE! Study Fairs

Southampton | Bristol

University of Leeds Featured PhD Programmes
Anglia Ruskin University Featured PhD Programmes
University of Warwick Featured PhD Programmes
University of Glasgow Featured PhD Programmes
University of Leeds Featured PhD Programmes

MRC DiMeN Doctoral Training Partnership: Boosting immunity in chronic lung disease and antimicrobial resistant infection via the IL-33-ST2 axis

This project is no longer listed in the FindAPhD
database and may not be available.

Click here to search the FindAPhD database
for PhD studentship opportunities
  • Full or part time
    Dr Simon Johnston
    Prof S Renshaw
    Dr A Humbles
  • Application Deadline
    No more applications being accepted
  • Competition Funded PhD Project (European/UK Students Only)
    Competition Funded PhD Project (European/UK Students Only)

Project Description

Macrophages are effector cells that directly kill microbes and regulatory cells that coordinate the wider immune response. Due to the complex nature of macrophage function, how their different roles are integrated during infection and inflammation is still poorly understood. Increased numbers of patients living with immunocompromise, chronic inflammatory disease and the threat of antimicrobial resistance means that new and improved treatments that modulate macrophage function are required. This project is a collaborative project between the Johnston lab at the University of Sheffield ( with an industrial partner, MedImmune (, that will use our ex vivo lung imaging approaches to address questions of macrophage function during infection and inflammation.

We have recently shown that the IL-33-ST2 axis plays a non-redundant role in regulating monocyte differentiation and alternative activated macrophage-mediated epithelial repair during naphthalene-induced injury of the airways (Dagner et al, in revision, Nat Immunol). In addition, macrophages from COPD patients demonstrate defective macrophage phagocytosis which may potentially contribute to why these patients suffer from repeated exacerbations which are linked with disease progression. We would like to extend these observations and determine whether IL-33-ST2 pathway is required for effective monocyte/macrophage recruitment, differentiation and function during lung infection.

We will use established in vivo infection challenge studies (e.g. Staphylococcal aureus, Streptococcus pneumoniae, Cryptococcal neoformans and influenza nasal inhalation route lung infection) coupled to ex vivo live fluorescent imaging of lung. We will use fluorescent labelled antibodies (eg. CCR2;ST2;MHCII;Ly6C;CD3;CD4;CD11c) to mark and distinguish recruited and differentiating immune cells. We will assess macrophage responses by measuring phagocytic capacity, intracellular killing and pathogen growth by time lapse imaging.

This PhD position offers an opportunity to work in a vibrant and successful biomedical research laboratory at The University of Sheffield with at least three months of industrial placement at our partner MedImmune. The Johnston lab is focused on the study infectious disease to improve patient treatment and to understand the fundamental mechanisms of how the immune system functions to fight infection. We use a diverse set of experimental models to understand human disease and collaborate with physicists, clinicians and engineers. This PhD position will give you the opportunity to learn a range of techniques and skills in biomedical research as well as broader training in research science. As an iCASE PhD student you will have the additional opportunity of working with MedImmune and seeing the benefits of partnering academic research with the development new treatments in industry.

Benefits of being in the DiMeN DTP:
This project is part of the Discovery Medicine North Doctoral Training Partnership (DiMeN DTP), a diverse community of PhD students across the North of England researching the major health problems facing the world today. Our partner institutions (Universities of Leeds, Liverpool, Newcastle and Sheffield) are internationally recognised as centres of research excellence and can offer you access to state-of the-art facilities to deliver high impact research.
We are very proud of our student-centred ethos and committed to supporting you throughout your PhD. As part of the DTP, we offer bespoke training in key skills sought after in early career researchers, as well as opportunities to broaden your career horizons in a range of non-academic sectors.
Being funded by the MRC means you can access additional funding for research placements, international training opportunities or internships in science policy, science communication and beyond. See how our current DiMeN students have benefited from this funding here:
Further information on the programme can be found on our website:

Funding Notes

iCASE Award: Industrial partnership project
Fully funded by the MRC for 3.5yrs, including a minimum of 3 months working within the industry partner. Enhanced stipend, tuition fees and budget for consumables, travel and subsistence.
Studentships commence: 1st October 2019.

To qualify, you must be a UK or EU citizen who has been resident in the UK/EU for 3 years prior to commencement. Applicants must have obtained, or be about to obtain, at least a 2.1 honours degree (or equivalent) in a relevant subject. All applications are scored blindly based on merit. Please read additional guidance here:
Good luck.

How good is research at University of Sheffield in Biological Sciences?

FTE Category A staff submitted: 44.90

Research output data provided by the Research Excellence Framework (REF)

Click here to see the results for all UK universities

FindAPhD. Copyright 2005-2019
All rights reserved.