Projects per year
Personal profile
Biography
Robyn works in the Faculty of Medicine, Nursing and Health Sciences at Monash University as a Professor. She is the Director of Education in the Central Clinical School of Monash University. She plays a major role in teaching Immunology to Science, Biomedical, and Medical undergraduate and post-graduate students at Monash University. For her contribution to teaching, Slattery received the Monash Central Clinical School Award for Excellence in Teaching in 2015, the Inaugural Teacher Innovation and Impact Award from the Monash University Office of Learning and Teaching in 2016 and the Monash Student Association (MSA) Teaching Award for Outstanding Teaching for the Faculty of Medicine Nursing and Health Sciences in 2016.
Robyn’s research background is in Immunology with a particular interest in using genetic engineering and interdisciplinary approaches. She undertook her PhD training at the Walter and Eliza Hall Institute under the supervision of Professor Jacques Miler, the forefather of modern immunology, who discovered the function of the thymus, T and B cells – this year winning the Lasker Prize – also known as the American Nobel! She has spent 25 years, at DNAX Research institute, USA, The John Curtin School of Medical Research, Australia, and Monash University, Australia, developing genetic engineering tools for their application in the discipline of immunology. This pioneering work was initially published in Nature with numerous follow-up publications in Proceedings of the National Academy of Science (PNAS) demonstrated that the direct interaction of cytotoxic cells of the immune system with the insulin-producing beta cells is a late event in the disease process, and the killer T cells responsible for destroying the insulin producing cells do not require direct contact with the insulin producing beta cells in order to become primed. These findings remain of paramount importance in understanding disease initiation for the rational design of immunomodulatory preventative strategies. Robyn’s research team at Monash, together with international collaborator Prof Pere Santamaria University of Calgary, has continued to pursue the mechanisms by which MHC class I and class II haplotypes confer susceptibility; most recently demonstrating that MHC class I expression on the dendritic cells (DCs) controls the presence and retention of cytotoxic T cells within the islet milieu, and that the specific haplotypes of MHC class II, expressed by these DCs control the development of regulatory T cells that prevent T1D. Since taking on a leadership role in education, Robyn’s research interests are now collaborative, continuing in the interdisciplinary theme, involving the development of instrumentation with the Engineering department and the utilization of infra-red microscopy approaches from the Chemistry department, to probe the phenotype of immune cells.
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
Research area keywords
- Education
- Immunology
- Diabetes
Projects
- 8 Finished
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Dietary intake of highly processed foods as a contributor to type 1 diabetes
Slattery, R. & Forbes, J.
National Health and Medical Research Council (NHMRC) (Australia)
1/01/12 → 31/12/14
Project: Research
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Prorenin and prorenin receptor in diabetic retinopathy: involvement of the Wnt pathway and inflammation
Wilkinson-Berka, J., Miller, A., Slattery, R. & Campbell, D.
National Health and Medical Research Council (NHMRC) (Australia)
1/01/11 → 31/12/13
Project: Research
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The role of MHC Class I expression on pancreatic ductal lineage cells in the pathogenesis of Type 1 Diabetes (T1D).
Slattery, R. & Miller, J.
National Health and Medical Research Council (NHMRC) (Australia)
1/01/10 → 31/03/13
Project: Research
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The role of the human insulin promoter in regulating beta cell autoimmunity
Slattery, R., Chan, F. Y., Milionis, A. & Serwecinska, L.
Juvenile Diabetes Research Foundation (JDRF) (United States of America)
1/03/07 → 28/02/09
Project: Research
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Perinatal exposure to high dietary advanced glycation end products in transgenic NOD8.3 mice leads to pancreatic beta cell dysfunction
Borg, D. J., Yap, F. Y. T., Keshvari, S., Simmons, D. G., Gallo, L. A., Fotheringham, A. K., Zhuang, A., Slattery, R. M., Hasnain, S. Z., Coughlan, M. T., Kantharidis, P. & Forbes, J. M., 2 Jan 2018, In: Islets. 10, 1, p. 10-24 15 p.Research output: Contribution to journal › Article › Research › peer-review
Open AccessFile18 Citations (Scopus) -
Vaccination with altered peptide ligands of a Plasmodium berghei circumsporozoite protein CD8 T-cell epitope: A model to generate T cells resistant to immune interference by polymorphic epitopes
Minigo, G., Flanagan, K. L., Slattery, R. M. & Plebanski, M., 14 Feb 2017, In: Frontiers in Immunology. 8, FEB, 115.Research output: Contribution to journal › Article › Research › peer-review
Open AccessFile1 Citation (Scopus) -
Perforin facilitates beta cell killing and regulates autoreactive CD8+ T-cell responses to antigen in mouse models of type 1 diabetes
Trivedi, P., Graham, K. L., Krishnamurthy, B., Fynch, S., Slattery, R. M., Kay, T. W. H. & Thomas, H. E., 1 Apr 2016, In: Immunology and Cell Biology. 94, 4, p. 334-341 8 p.Research output: Contribution to journal › Article › Research › peer-review
18 Citations (Scopus) -
The NF-κB transcription factor RelA is required for the tolerogenic function of Foxp3+ regulatory T cells
Messina, N., Fulford, T., O'Reilly, L., Loh, W. X., Motyer, J. M., Ellis, D., McLean, C., Naeem, H., Lin, A., Gugasyan, R., Slattery, R. M., Grumont, R. J. & Gerondakis, S., Jun 2016, In: Journal of Autoimmunity. 70, p. 52-62 11 p.Research output: Contribution to journal › Article › Research › peer-review
41 Citations (Scopus) -
Advances in our understanding of the pathophysiology of Type 1 diabetes: lessons from the NOD mouse
Jayasimhan, A., Mansour, K. P. & Slattery, R. M., 2014, In: Clinical Science. 126, 1, p. 1 - 18 18 p.Research output: Contribution to journal › Article › Research › peer-review
48 Citations (Scopus)