Dr Nicole Wittwer

School of Medicine

College of Health

Eligible to supervise Masters and PhD - email supervisor to discuss availability.


Dr Nicole Wittwer is a postdoctoral researcher in the Translational Oncology Laboratory at the Centre for Cancer Biology. She has a keen interest in the immune system and how we can modulate the immune system to fight back against cancer.
Dr Wittwer completed her PhD at the University of South Australia in the laboratory of Professor Angel Lopez, investigating the role of the stem cell marker CD123 in acute myeloid leukaemia. She then undertook a post-doctoral position at a highly successful Biotechnology company, Bionomics Ltd. As a member of the Oncology team, she worked on drug discovery and development programs and contributed to the identification and development of pharmacodynamic biomarkers directly in support of a phase I clinical trial in metastatic colorectal cancer.
Dr Wittwer is now based in the Translational Oncology Laboratory headed by Professor Michael Brown. The Translational Oncology Laboratory aims to develop new approaches to modulate the body’s immune system to more effectively target cancer cells and to translate these research discoveries into the clinic. Her research focuses on understanding how cancer cells override our immune defences and using this knowledge to develop therapeutic approaches to overcome immune resistance and sensitise cancer cells to therapy. Recent projects have focused on combining antibody drug conjugates with immunotherapy in breast and colon cancer in collaboration with Bristol Myers Squibb and the development of Chimeric Antigen Receptor (CAR) T-cells targeting a novel antigen in pancreatic cancer.

Date Institution name Country Title
University of South Australia Australia Doctor of Philosopy
University of South Australia Australia Bachelor of Laboratory Medicine with Honours

Year Citation
2025 Liapis, V., Wittwer, N. L., Tieu, W., Gargett, T., Brown, M. P., & Staudacher, A. H. (2025). Detection of immune-mediated tumour cell death in vivo using Zirconium-89-labeled APOMAB®. Journal of Translational Medicine, 23(1, article no. 651), 651-1-651-18.
DOI Scopus1 WoS1 Europe PMC1
2024 Gargett, T., Truong, N. T. H., Gardam, B., Yu, W., Ebert, L. M., Johnson, A., . . . Brown, M. P. (2024). Safety and biological outcomes following a phase 1 trial of GD2-specific CAR-T cells in patients with GD2-positive metastatic melanoma and other solid cancers. Journal for ImmunoTherapy of Cancer, 12(5), e008659-1-e008659-17.
DOI Scopus33 WoS31 Europe PMC26
2023 Wittwer, N. L., Staudacher, A. H., Liapis, V., Cardarelli, P., Warren, H., & Brown, M. P. (2023). An anti-mesothelin targeting antibody drug conjugate induces pyroptosis and ignites antitumor immunity in mouse models of cancer. Journal for ImmunoTherapy of Cancer, 11(3), e006274-1-e006274-16.
DOI Scopus23 WoS25 Europe PMC17
2023 Wittwer, N. L., Brown, M. P., Liapis, V., & Staudacher, A. H. (2023). Antibody drug conjugates: hitting the mark in pancreatic cancer?. Journal of Experimental and Clinical Cancer Research, 42(1, article no. 280), 280-1-280-16.
DOI Scopus24 WoS21 Europe PMC19
2022 Nazarizadeh, A., Staudacher, A. H., Wittwer, N. L., Turnbull, T., Brown, M. P., & Kempson, I. (2022). Aluminium Nanoparticles as Efficient Adjuvants Compared to Their Microparticle Counterparts: Current Progress and Perspectives. International Journal of Molecular Sciences, 23(9), 4707-1-4707-15.
DOI Scopus36 WoS32 Europe PMC26
2022 Staudacher, A. H., Liapis, V., Wittwer, N. L., Tieu, W., Lam, H. C., Leusen, J., & Brown, M. P. (2022). Fc gamma receptor is not required for in vivo processing of radio- and drug-conjugates of the dead tumor cell-targeting monoclonal antibody, APOMAB®. Biomedicine and Pharmacotherapy, 151(article no. 113090), 113090-1-113090-10.
DOI WoS1
2022 Gargett, T., Ebert, L. M., Truong, N. T. H., Kollis, P. M., Sedivakova, K., Yu, W., . . . Brown, M. P. (2022). GD2-targeting CAR-T cells enhanced by transgenic IL-15 expression are an effective and clinically feasible therapy for glioblastoma. Journal for ImmunoTherapy of Cancer, 10(9), 1-15.
DOI Scopus79 WoS79 Europe PMC75
2021 Liapis, V., Tieu, W., Wittwer, N. L., Gargett, T., Evdokiou, A., Takhar, P., . . . Staudacher, A. H. (2021). Positron emission tomographic imaging of tumor cell death using zirconium-89-labeled APOMAB® following cisplatin chemotherapy in lung and ovarian cancer xenograft models. Molecular Imaging and Biology, 23(6), 914-928.
DOI Scopus8 WoS9 Europe PMC6
2021 Liapis, V., Tieu, W., Wittwer, N. L., Gargett, T., Evdokiou, A., Takhar, P., . . . Staudacher, A. H. (2021). Correction to: Positron Emission Tomographic Imaging of Tumor Cell Death Using Zirconium-89-Labeled APOMAB® Following Cisplatin Chemotherapy in Lung and Ovarian Cancer Xenograft Models (Molecular Imaging and Biology, (2021), 23, 6, (914-928), 10.1007/s11307-021-01620-1). Molecular Imaging and Biology, 23(6), 929.
DOI
2020 Staudacher, A. H., Liapis, V., Tieu, W., Wittwer, N., & Brown, M. P. (2020). Tumour-associated macrophages process drug and radio-conjugates of the dead tumour cell-targeting APOMAB® antibody. Journal of Controlled Release, 327, 779-787.
DOI Scopus9 WoS10 Europe PMC8
2020 Liapis, V., Tieu, W., Rudd, S. E., Donnelly, P. S., Wittwer, N. L., Brown, M. P., & Staudacher, A. H. (2020). Improved non-invasive positron emission tomographic imaging of chemotherapy-induced tumor cell death using Zirconium-89-labeled APOMAB®. EJNMMI Radiopharmacy and Chemistry, 5(1), 27-1-27-15.
DOI Scopus11 WoS13 Europe PMC10
2017 Wittwer, N. L., Brumatti, G., Marchant, C., Sandow, J. J., Pudney, M. K., Dottore, M., . . . Ramshaw, H. S. (2017). High CD123 levels enhance proliferation in response to IL-3, but reduce chemotaxis by downregulating CXCR4 expression. Blood Advances, 1(15), 1067-1079.
DOI Scopus33 WoS31 Europe PMC25

Year Citation
2018 Inglis, D. J., Licari, J., Georgiou, K. R., Wittwer, N. L., Hamilton, R. W., Beaumont, D. M., . . . Lavranos, T. C. (2018). Characterization of BNC101 a human specific monoclonal antibody targeting the GPCR LGR5: First-in-human evidence of target engagement. In CANCER RESEARCH Vol. 78 (pp. 1 page). Chicago, IL: AMER ASSOC CANCER RESEARCH.
DOI WoS8

Year Citation
2022 Gargett, T., Ebert, L., Truong, N. T. H., Kollis, P., Sedivakova, K., Yu, W., . . . Brown, M. (2022). GD2-targeting CAR-T cells enhanced by transgenic IL-15 expression are an effective and clinically feasible therapy for glioblastoma.
DOI
  • Investigating dual targeting GD2 and FAP CAR T-cells for the treatment of brain malignancies, Neurosurgical Research Foundation, 01/10/2025 - 30/09/2026

Date Role Research Topic Program Degree Type Student Load Student Name
2025 Co-Supervisor - Doctor of Philosophy Doctorate Full Time Miss Bhumika Tirthani
2024 Principal Supervisor Investigating dual targeting CAR-T cells for the treatment of brain tumours Doctor of Philosophy Doctorate Full Time Miss Abbey Rose Marshall
2024 Principal Supervisor Investigating dual targeting CAR-T cells for the treatment of brain tumours Doctor of Philosophy Doctorate Full Time Miss Abbey Rose Marshall

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