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    Metabolic regulation of anti-tumour T cell immunity
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    University of Leeds

    Metabolic regulation of anti-tumour T cell immunity

    University of Leeds

    University of Leeds

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    United Kingdom, Leeds

    University RankQS Ranking
    83

    Key Facts

    Program Level

    PhD (Philosophy Doctorate)

    Study Type

    Full Time

    Delivery

    On Campus

    Campuses

    Main Site

    Program Language

    English

    Start & Deadlines

    Next Intake Deadlines
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    Metabolic regulation of anti-tumour T cell immunity

    About

    Summary

    The induction of effective immune responses to tumours can provide long-lasting protection from cancer. In this regard, cytotoxic CD8+ T cells can suppress tumour growth by directly killing cancer cells and also by producing inflammatory cytokines. However, in many individuals the T cell response to cancer is ineffective. Several factors underlie the failure to mount protective immunity to cancer. Firstly, T cell responses can be suppressed by the inhibitory tumour environment. Secondly, tumour antigens are often perceived by the immune system as being identical to normal “self” tissue, and therefore a T cell response is not strongly induced. Therefore, it is clear that in order to improve patient outcomes and therapeutic opportunities in cancer, we need to understand how immune responses to tumours are regulated.

    Full description

    The aim of this project is to investigate how T cells integrate antigenic, cytokine and environmental signals, particularly in the context of the tumour microenvironment. A key approach will be to determine how fundamental cellular metabolic pathways regulate T cell activation and effector function. This will be tested using in vitro and ex vivo analyses of transgenic mouse T cells. In vitro cellular immunology and biochemical techniques will complement in vivo mouse studies. A further aim to be to understand how these pathways are regulated in human T cells. This project is suitable for students with a strong background and interest in immunology, biochemistry, molecular biology or cell biology.

    References:

    1. Salmond RJ, Brownlie RJ, Morrison VL, Zamoyska R. 2014. The tyrosine phosphatase PTPN22 discriminates weak self peptides from strong agonist TCR signals. Nat. Immunol. 15(9):875-883.
    2. Brownlie RJ, Garcia C, Ravasz M, Zehn D, Salmond RJ, Zamoyska R. 2017. Resistance to TGFβ suppression and improved anti-tumor responses in CD8+ T cells lacking PTPN22. Nat. Commun. 8(1):1343.

    Requirements

    Entry Requirements

    A degree in biological sciences, dentistry, medicine, midwifery, nursing, psychology or a good honours degree in a subject relevant to the research topic. A Masters degree in a relevant subject may also be required in some areas of the Faculty. For entry requirements for all other research degrees we offer, please contact us.

    English Program Requirements

    Applicants whose first language is not English must provide evidence that their English language is sufficient to meet the specific demands of their study. The Faculty of Medicine and Health minimum requirements in IELTS and TOEFL tests for PhD, MSc, MPhil, MD are: • British Council IELTS - score of 6.5 overall, with no element less than 6.0 • TOEFL iBT - overall score of 92 with the listening and reading element no less than 21, writing element no less than 22 and the speaking element no less than 23.

    Fee Information

    Tuition Fee

    GBP 0 

    Application Fee

    GBP  
    University of Leeds

    Metabolic regulation of anti-tumour T cell immunity

    University of Leeds

    [object Object]

    United Kingdom,

    Leeds

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