Joining US
We are looking for new group members with passion, talent, and grit! You will have the chance to work on grand challenges in the field of immune regulation and tumour immunity. You will be responsible for driving your research, identifying the most important questions, designing and performing experiments and publishing findings. We are happy to consider and support applications for talented postdoctoral researchers, PhD and Master's students. Please send me an email stating briefly why you are interested in joining the group and attaching a CV.
Jie Yang
BVetMed, PhD
Junior Group Leader
Group Leader - T cell immunity and immunosuppression in cancer
Biography
I originally trained in Veterinary Medicine before undertaking a PhD in Immunology at the Roslin Institute in the University of Edinburgh. Following postdoctoral work at the Francis Crick Institute and the University of Cambridge, I joined the Centre for Immuno-Oncology at the University of Oxford as a Group Leader in 2025.
A major contribution of our research was discovery of the mechanisms underlying the anti-metastatic effects of aspirin. Our work demonstrated that inhibitors of cyclooxygenase 1 (COX-1), including aspirin, enhance immunity to cancer metastasis by releasing T cells from suppression by platelet-derived thromboxane A2 (Yang et al., Nature 2025). These findings have contributed to understanding of clinical observations of aspirin’s anti-metastatic effects and received widespread media attention including BBC News. This work is particularly timely as it provides mechanistic insight for new randomised controlled trials including CaPP3 and Add-Aspirin, which are investigating the efficacy of low-dose aspirin in cancer prevention and recurrence.
Our research aims to uncover the molecular and cellular mechanisms underpinning immune regulation and cancer immunosuppression, with the goal of developing new approaches for cancer prevention and treatment of metastatic disease. Our work combines cutting-edge mouse models, advanced cellular and molecular techniques, and translational approaches to understand how the immune system can be harnessed for cancer prevention and treatment. Fundamental discoveries in immune suppression mechanisms will pave the way for new preventive and therapeutic strategies that could transform outcomes for patients at risk of developing cancer or those with existing metastatic disease.
Recent publications
Fine-tuning BACH2 dosage balances stemness and effector function to enhance antitumor T cell therapy.
Journal article
Conti AG. et al, (2026), Nature immunology, 27, 436 - 451
Aspirin prevents metastasis by limiting platelet TXA2 suppression of T cell immunity.
Journal article
Yang J. et al, (2025), Nature, 640, 1052 - 1061
IFNγ Production by Functionally Reprogrammed Tregs Promotes Antitumor Efficacy of OX40/CD137 Bispecific Agonist Therapy.
Journal article
Imianowski CJ. et al, (2024), Cancer research communications, 4, 2045 - 2057
Acquisition of suppressive function by conventional T cells limits antitumor immunity upon Treg depletion.
Journal article
Whiteside SK. et al, (2023), Science immunology, 8
IL-2 is inactivated by the acidic pH environment of tumors enabling engineering of a pH-selective mutein.
Journal article
Gaggero S. et al, (2022), Science immunology, 7
BACH2 restricts NK cell maturation and function, limiting immunity to cancer metastasis.
Journal article
Imianowski CJ. et al, (2022), The Journal of experimental medicine, 219
CCR8 marks highly suppressive Treg cells within tumours but is dispensable for their accumulation and suppressive function.
Journal article
Whiteside SK. et al, (2021), Immunology, 163, 512 - 520
A cell-based bioluminescence assay reveals dose-dependent and contextual repression of AP-1-driven gene expression by BACH2.
Journal article
Vardaka P. et al, (2020), Scientific reports, 10
BACH2 drives quiescence and maintenance of resting Treg cells to promote homeostasis and cancer immunosuppression.
Journal article
Grant FM. et al, (2020), The Journal of experimental medicine, 217
A distal enhancer at risk locus 11q13.5 promotes suppression of colitis by Treg cells.
Journal article
Nasrallah R. et al, (2020), Nature, 583, 447 - 452
Granzyme B Is an Essential Mediator in CD8+ T Cell Killing of Theileria parva-Infected Cells.
Journal article
Yang J. et al, (2019), Infection and immunity, 87, e00386 - e00318
Identification and annotation of bovine granzyme genes reveals a novel granzyme encoded within the trypsin-like locus.
Journal article
Yang J. et al, (2018), Immunogenetics, 70, 585 - 597
IL-7-dependent maintenance of ILC3s is required for normal entry of lymphocytes into lymph nodes.
Journal article
Yang J. et al, (2018), The Journal of experimental medicine, 215, 1069 - 1077