Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

NDORMS DPhil & MSc by Research


With extension of the average lifespan, the ageing population has become a heavy burden for both society and individuals. Immune responses, key for the removal of pathogens and damage, are compromised in the elderly, making the elderly more susceptible to infections. In addition immune senescence is a risk factor for many late-onset diseases, such as cancer and atherosclerosis. Autophagy through degrading bulk cytoplasmic material maintains cytoplasmic health and cellular homeostasis [1]. We have found that it allows differentiation of immune cells [2, 3] [4]. In previous work we showed that loss of autophagy in macrophages results in low-grade inflammation (inflamm-aging) and reduces innate and adaptive immune responses, typical of a senescent immune system [5]. Autophagy induction rejuvenates immune responses in the elderly in T cells [6]. We have recently uncovered a novel pathway that controls the translation of autophagy proteins in T and B lymphocytes. Lymphocytes from old mice and elderly humans have reduced expression of key molecules in this pathway, making it also a to-date undescribed aging pathway. In this project we will further define its molecular signaling elements using a variety of techniques including 18-parameter flow cytometry, transcriptomics, ribosome profiling, Image Stream, confocal microscopy, transgenic mouse models and microbiota metabolite profiling. As it is a druggable pathway, this will pave the way for the development of a novel mTOR independent drug that is capable of modulating autophagy.


The Kennedy Institute is a world-renowned research centre, housed in a brand new, state-of-the-art facility at the University of Oxford. The Simon lab consists of 3 postdocs, 2 DPhils students in their final year and 2 DPhil students who started in October 2017. We regularly welcome MSC students and other short-term students in the lab, so there will be opportunities to train your supervision skills. It is a small, friendly and very international lab. Even though lab members are ambitious, the general attitude is not competitive and lab members are encouraged to help each other out. Every DPhil student so far has had the opportunity to write a review, and has published a first author paper. We collaborate locally, nationally and internationally. The presentation of data at national and international conferences is encouraged.


A core curriculum of lectures will be taken in the first term to provide a solid foundation in a broad range of subjects including inflammation, epigenetics, translational immunology and data analysis.

Students will attend weekly seminars within the department and those relevant in the wider University. Students will be expected to present data regularly to the department and to the Simon group in lab meetings. 


  1. Zhang, H., D.J. Puleston, and A.K. Simon, Autophagy and Immune Senescence. Trends Mol Med, 2016. 22(8): p. 671-86
  2. Riffelmacher, T. and A.K. Simon, Mechanistic roles of autophagy in hematopoietic differentiation. FEBS J, 2017. 284(7): p. 1008-1020
  3. Riffelmacher, T., A. Clarke, F. Richter, A. Stranks, S. Pandey, S. Danielli, . . . A. Simon, Autophagy-dependent generation of free fatty acids is critical for normal neutrophil differentiation. Immunity, 2017. in press
  4. Mortensen, M., E.J. Soilleux, G. Djordjevic, R. Tripp, M. Lutteropp, E. Sadighi-Akha, . . . A.K. Simon, The autophagy protein Atg7 is essential for hematopoietic stem cell maintenance. J Exp Med, 2011. 208(3): p. 455-67.PMC3058574
  5. Stranks, A.J., A.L. Hansen, I. Panse, M. Mortensen, D.J. Ferguson, D.J. Puleston, . . . A.K. Simon, Autophagy Controls Acquisition of Aging Features in Macrophages. J Innate Immun, 2015. 7(4): p. 375-91
  6. Puleston, D.J., H. Zhang, T.J. Powell, E. Lipina, S. Sims, I. Panse, . . . A.K. Simon, Autophagy is a critical regulator of memory CD8(+) T cell formation. Elife, 2014. 3.PMC4225493

Please contact Professor Katja Simon ( if you would like to enquire about the project or discuss other aspects of your application. 

How to Apply

The department accepts applications throughout the year but it is recommended that, in the first instance, you contact the relevant supervisor(s) or the Graduate Studies Officer ( who will be able to advise you of the essential requirements.

Interested applicants should have or expect to obtain a first or upper second class BSc degree or equivalent, and will also need to provide evidence of English language competence. The University requires candidates to formally apply online and for their referees to submit online references via the online application system.

The application guide and form is found online and the DPhil or MSc by research will commence in October 2018.

When completing the online application, please read the University Guide.

Project reference number #NDORMS-2018/10


Full list


Find out more