
Overview
Background
Gabrielle Belz originally trained in veterinary medicine and surgery and received her PhD in understanding the organisation of lymphatics and lymphoid tissues at The University of Queensland. After a short stint in Canada to work on B cells, she moved to St Jude Children’s Research Hospital to work with Peter Doherty supported by an NHMRC CJ Martin Fellowship. Here she established a number of systems that now allow tracking of virus-specific T cells and established the paradigm changing notion that CD4 T cell help was required for generating antiviral responses. She returned to The Walter and Eliza Hall Institute of Medical Research and uncovered the identity of the key dendritic cells necessary for initiating antiviral infections. Subsequently she was awarded the Burnet Prize and NHMRC Elizabeth Blackburn Fellowship. Her research contributions have been recognized by a number of awards including a Wellcome Trust Overseas Fellowship, HHMI international fellowship, ARC Future fellowship, Doctor of Veterinary Science, the Gottschalk Medal (Australian Academy of Science) and in 2024 an ARC Laureate Fellowship. Her laboratory focuses on deciphering the key cellular and transcriptional signals of protective immunity particularly by T cells and in understanding how innate immune cells develop and make novel contributions to mucosal immune defence.
Availability
- Professor Gabrielle Belz is:
- Available for supervision
Fields of research
Qualifications
- Bachelor of Veterinary Biology, The University of Queensland
- Bachelor (Honours) of Veterinary Science, The University of Queensland
- Doctor of Philosophy, The University of Queensland
- Doctoral Diploma, The University of Queensland
Research impacts
Overall goals:
Our work aims to understand how the immune system responds to infections including viruses, bacteria and parasites.
We are elucidating how different types of immune cells develop, and what factors influences their decision to become one type of immune cell or another.
Understanding how the body deals with pathogens will give clues about how to enhance protective immunity. Our goal is to discover new therapies that boost our immune system to protect against infection.
Research interests:
Cell differentiation is the process by which cells develop and mature. In this process, cells become more specialised and acquire potent effector functions that allow them to eliminate infectious organisms. There is an urgent need to develop new therapies that focus on augmenting host immunity.
Our research focuses on:
- Elucidating the mechanisms responsible for the generation of protective immunity in response to lung and gastrointestinal pathogens
- How protective immunity breaks down in chronic overwhelming infections
- Identifying factors that can promote host immune responses and potent long-lived protective immunological memory.
We have developed and use a number of in vivo models of infectious diseases including:
- Influenza
- Herpes virus
- Lymphocytic choriomeningitis virus (LCMV)
These models provide us with an unprecedented opportunity to examine the mechanisms that these pathogens employ to infect hosts and elicit immune protection or to subvert the host responses. Using a variety of approaches including multiparameter flow cytometry, systems biology and global gene expression profiling we aim to define cellular and transcriptional pathways in normal memory T cell differentiation, innate immune cell subsets and immune failure.
Works
Search Professor Gabrielle Belz’s works on UQ eSpace
2015
Journal Article
c-Myb is required for plasma cell migration to bone marrow after immunization or infection
Good-Jacobson, Kim L., O'Donnell, Kristy, Belz, Gabrielle T., Nutt, Stephen L. and Tarlinton, David M. (2015). c-Myb is required for plasma cell migration to bone marrow after immunization or infection. Journal of Experimental Medicine, 212 (7), 1001-1009. doi: 10.1084/jem.20150191
2015
Journal Article
SOCS4 is dispensable for an efficient recall response to influenza despite being required for primary immunity
Kedzierski, Lukasz, Clemens, E Bridie, Bird, Nicola L., Kile, Benjamin T., Belz, Gabrielle T., Nicola, Nicos A., Kedzierska, Katherine and Nicholson, Sandra E. (2015). SOCS4 is dispensable for an efficient recall response to influenza despite being required for primary immunity. Immunology and Cell Biology, 93 (10), 909-913. doi: 10.1038/icb.2015.55
2015
Journal Article
Bcl11b is essential for group 2 innate lymphoid cell development
Walker, Jennifer A., Oliphant, Christopher J., Englezakis, Alexandros, Yu, Yong, Clare, Simon, Rodewald, Hans-Reimer, Belz, Gabrielle, Liu, Pentao, Fallon, Padraic G. and McKenzie, Andrew N.J. (2015). Bcl11b is essential for group 2 innate lymphoid cell development. Journal of Experimental Medicine, 212 (6), 875-882. doi: 10.1084/jem.20142224
2015
Journal Article
T-box Transcription Factors Combine with the Cytokines TGF-β and IL-15 to Control Tissue-Resident Memory T Cell Fate
Mackay, Laura K., Wynne-Jones, Erica, Freestone, David, Pellicci, Daniel G., Mielke, Lisa A., Newman, Dane M., Braun, Asolina, Masson, Frederick, Kallies, Axel, Belz, Gabrielle T. and Carbone, Francis R. (2015). T-box Transcription Factors Combine with the Cytokines TGF-β and IL-15 to Control Tissue-Resident Memory T Cell Fate. Immunity, 43 (6), 1101-1111. doi: 10.1016/j.immuni.2015.11.008
2015
Journal Article
Immunology and Cell Biology Publication of the Year Awards 2014
Belz, Gabrielle (2015). Immunology and Cell Biology Publication of the Year Awards 2014. Immunology and Cell Biology, 93 (10), 837-838. doi: 10.1038/icb.2015.86
2014
Journal Article
Antigen affinity, costimulation, and cytokine inputs sum linearly to amplify T cell expansion
Marchingo, Julia M., Kan, Andrey, Sutherland, Robyn M., Duffy, Ken R., Wellard, Cameron J., Belz, Gabrielle T., Lew, Andrew M., Dowling, Mark R., Heinzel, Susanne and Hodgkin, Philip D. (2014). Antigen affinity, costimulation, and cytokine inputs sum linearly to amplify T cell expansion. Science, 346 (6213), 1123-1127. doi: 10.1126/science.1260044
2014
Journal Article
Peripheral natural killer cell maturation depends on the transcription factor Aiolos
Holmes, Melissa L., Huntington, Nicholas D., Thong, Rebecca P. L., Brady, Jason, Hayakawa, Yoshihiro, Andoniou, Christopher E., Fleming, Peter, Shi, Wei, Smyth, Gordon K., Degli-Esposti, Mariapia A., Belz, Gabrielle T., Kallies, Axel, Carotta, Sebastian, Smyth, Mark J. and Nutt, Stephen L. (2014). Peripheral natural killer cell maturation depends on the transcription factor Aiolos. EMBO Journal, 33 (22), 2721-2734. doi: 10.15252/embj.201487900
2014
Journal Article
Innate immunodeficiency following genetic ablation of Mcl1 in natural killer cells
Sathe, Priyanka, Delconte, Rebecca B., Souza-Fonseca-Guimaraes, Fernando, Seillet, Cyril, Chopin, Michael, Vandenberg, Cassandra J., Rankin, Lucille C., Mielke, Lisa A., Vikstrom, Ingela, Kolesnik, Tatiana B., Nicholson, Sandra E., Vivier, Eric, Smyth, Mark J., Nutt, Stephen L., Glaser, Stefan P., Strasser, Andreas, Belz, Gabrielle T., Carotta, Sebastian and Huntington, Nicholas D. (2014). Innate immunodeficiency following genetic ablation of Mcl1 in natural killer cells. Nature Communications, 5 (1) 4539, 1-10. doi: 10.1038/ncomms5539
2014
Journal Article
Id2 represses E2A-mediated activation of IL-10 expression in T cells
Masson, Frederick, Ghisi, Margherita, Groom, Joanna R., Kallies, Axel, Seillet, Cyril, Johnstone, Ricky W., Nutt, Stephen L. and Belz, Gabrielle T. (2014). Id2 represses E2A-mediated activation of IL-10 expression in T cells. Blood, 123 (22), 3420-3428. doi: 10.1182/blood-2014-03-561456
2014
Journal Article
A Murid gamma-herpesviruses exploits normal splenic immune communication routes for systemic spread
Frederico, B., Chao, B., May, J.S., Belz, G.T. and Stevenson, P.G. (2014). A Murid gamma-herpesviruses exploits normal splenic immune communication routes for systemic spread. Cell Host and Microbe, 15 (4), 457-470. doi: 10.1016/j.chom.2014.03.010
2014
Journal Article
Transcription factor IRF4 regulates germinal center cell formation through a B cell-intrinsic mechanism
Willis, Simon N., Good-Jacobson, Kim L., Curtis, Joan, Light, Amanda, Tellier, Julie, Shi, Wei, Smyth, Gordon K., Tarlinton, David M., Belz, Gabrielle T., Corcoran, Lynn M., Kallies, Axel and Nutt, Stephen L. (2014). Transcription factor IRF4 regulates germinal center cell formation through a B cell-intrinsic mechanism. Journal of Immunology, 192 (7), 3200-3206. doi: 10.4049/jimmunol.1303216
2014
Journal Article
Differential requirement for Nfil3 during NK cell development
Seillet C., Huntington N.D., Gangatirkar P., Axelsson E., Minnich M., Brady H.J.M., Busslinger M., Smyth M.J., Belz G.T. and Carotta S. (2014). Differential requirement for Nfil3 during NK cell development. Journal of Immunology, 192 (6), 2667-2676. doi: 10.4049/jimmunol.1302605
2014
Journal Article
Fas ligand-mediated immune surveillance by T cells is essential for the control of spontaneous B cell lymphomas
Afshar-Sterle, Shoukat, Zotos, Dimitra, Bernard, Nicholas J., Scherger, Anna K., Roedling, Lisa, Alsop, Amber E., Walker, Jennifer, Masson, Frederick, Belz, Gabrielle T., Corcoran, Lynn M., O'Reilly, Lorraine A., Strasser, Andreas, Smyth, Mark J., Johnstone, Ricky, Tarlinton, David M., Nutt, Stephen L. and Kallies, Axel (2014). Fas ligand-mediated immune surveillance by T cells is essential for the control of spontaneous B cell lymphomas. Nature Medicine, 20 (3), 283-290. doi: 10.1038/nm.3442
2014
Journal Article
IL-17-producing NKT cells depend exclusively on IL-7 for homeostasis and survival
Webster, K. E., Kim, H. O., Kyparissoudis, K., Corpuz, T. M., Pinget, G. V., Uldrich, A. P., Brink, R., Belz, G. T., Cho, J. H., Godfrey, D. I. and Sprent, J. (2014). IL-17-producing NKT cells depend exclusively on IL-7 for homeostasis and survival. Mucosal Immunology, 7 (5), 1058-1067. doi: 10.1038/mi.2013.122
2014
Journal Article
Immunology and cell biology publication of the year awards 2013
Belz, Gabrielle (2014). Immunology and cell biology publication of the year awards 2013. Immunology and Cell Biology, 92 (10), 811-812. doi: 10.1038/icb.2014.92
2014
Journal Article
Suppressor of Cytokine Signaling 4 (SOCS4) protects against severe cytokine storm and enhances viral clearance during influenza infection
Kedzierski, Lukasz, Linossi, Edmond M., Kolesnik, Tatiana B., Day, E. Bridie, Bird, Nicola L., Kile, Benjamin T., Belz, Gabrielle T., Metcalf, Donald, Nicola, Nicos A., Kedzierska, Katherine and Nicholson, Sandra E. (2014). Suppressor of Cytokine Signaling 4 (SOCS4) protects against severe cytokine storm and enhances viral clearance during influenza infection. PLoS Pathogens, 10 (5) e1004134. doi: 10.1371/journal.ppat.1004134
2014
Journal Article
Nfil3 is required for the development of all innate lymphoid cell subsets
Seillet, Cyril, Rankin, Lucille C., Groom, Joanna R., Mielke, Lisa A., Tellier, Julie, Chopin, Michael, Huntington, Nicholas D., Belz, Gabrielle T. and Carotta, Sebastian (2014). Nfil3 is required for the development of all innate lymphoid cell subsets. Journal of Experimental Medicine, 211 (9), 1733-1740. doi: 10.1084/jem.20140145
2014
Journal Article
Erratum: The transcription factor IRF4 is essential for TCR affinity-mediated metabolic programming and clonal expansion of T cells (Nature Immunology (2013) 14 (1155-1165 ))
Man, Kevin, Miasari, Maria, Shi, Wei, Xin, Annie, Henstridge, Darren C., Preston, Simon, Pellegrini, Marc, Belz, Gabrielle T., Smyth, Gordon K., Febbraio, Mark A., Nutt, Stephen L. and Kallies, Axel (2014). Erratum: The transcription factor IRF4 is essential for TCR affinity-mediated metabolic programming and clonal expansion of T cells (Nature Immunology (2013) 14 (1155-1165 )). Nature Immunology, 15 (9), 894-894. doi: 10.1038/ni0914-894b
2013
Journal Article
Langerhans cells are generated by two distinct PU.1-dependent transcriptional networks
Chopin, Michaël, Seillet, Cyril, Chevrier, Stéphane, Wu, Li, Wang, Hongsheng, Morse III, Herbert C., Belz, Gabrielle T. and Nutt, Stephen L. (2013). Langerhans cells are generated by two distinct PU.1-dependent transcriptional networks. Journal of Experimental Medicine, 210 (13), 2967-2980. doi: 10.1084/jem.20130930
2013
Journal Article
Circulating precursor CCR7(lo)PD-1(hi) CXCR5(+) CD4(+) T cells indicate Tfh cell activity and promote antibody responses upon antigen reexposure
He, Jing, Tsai, Louis M., Leong, Yew Ann, Hu, Xin, Ma, Cindy S., Chevalier, Nina, Sun, Xiaolin, Vandenberg, Kirsten, Rockman, Steve, Ding, Yan, Zhu, Lei, Wei, Wei, Wang, Changqi, Karnowski, Alexander, Belz, Gabrielle T., Ghali, Joanna R., Cook, Matthew C., Riminton, D. Sean, Veillette, Andre, Schwartzberg, Pamela L., Mackay, Fabienne, Brink, Robert, Tangye, Stuart G., Vinuesa, Carola G., Mackay, Charles R., Li, Zhanguo and Yu, Di (2013). Circulating precursor CCR7(lo)PD-1(hi) CXCR5(+) CD4(+) T cells indicate Tfh cell activity and promote antibody responses upon antigen reexposure. Immunity, 39 (4), 770-781. doi: 10.1016/j.immuni.2013.09.007
Funding
Current funding
Supervision
Availability
- Professor Gabrielle Belz is:
- Available for supervision
Before you email them, read our advice on how to contact a supervisor.
Available projects
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Understanding mucosal immunity
The picture of the network governing the mucosal immunity and how the different immune populations interplay is only just emerging, but it is already opening a whole new array of exciting possibilities for immune regulation and immunotherapeutic strategies. Our current projects aim to provide a new dimension to this emerging field in understanding how mucosal epithelial cells interact with immune cells to drive mucosal immunosurveillance, homeostasis and immunity. We have developed a number of new tools to dissect this epithelial immune network and understand its regulation in immunity.
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Delineating long-term protective immunity to pathogen infection
Our work aims to understand how the immune system responds to infections including viruses, bacteria and parasites. We endeavour to elucidate how different types of immune cells develop, and what factors influences their decision to become one type of immune cell or another. Understanding how the body deals with pathogens will give clues about how to enhance protective immunity. Our goal is to discover new therapies that boost our immune system to protect against infection.
Our research focuses on:
- Elucidating the mechanisms responsible for the generation of protective immunity in response to lung and gastrointestinal pathogens including influenza, herpesvirus and intestinal bacterial infections
- How protective immunity breaks down in chronic overwhelming infections
- Identifying factors that can promote host immune responses and potent long-lived protective immunological memory
-
Understanding mucosal immunity
The picture of the network governing the mucosal immunity and how the different immune populations interplay is only just emerging, but it is already opening a whole new array of exciting possibilities for immune regulation and immunotherapeutic strategies. Our current projects aim to provide a new dimension to this emerging field in understanding how mucosal epithelial cells interact with immune cells to drive mucosal immunosurveillance, homeostasis and immunity. We have developed a number of new tools to dissect this epithelial immune network and understand its regulation in immunity.
-
Delineating long-term protective immunity to pathogen infection
Our work aims to understand how the immune system responds to infections including viruses, bacteria and parasites. We endeavour to elucidate how different types of immune cells develop, and what factors influences their decision to become one type of immune cell or another. Understanding how the body deals with pathogens will give clues about how to enhance protective immunity. Our goal is to discover new therapies that boost our immune system to protect against infection.
Our research focuses on:
- Elucidating the mechanisms responsible for the generation of protective immunity in response to lung and gastrointestinal pathogens including influenza, herpesvirus and intestinal bacterial infections
- How protective immunity breaks down in chronic overwhelming infections
- Identifying factors that can promote host immune responses and potent long-lived protective immunological memory
-
Unravelling immune signalling networks in mucosal immunity
Mucosal surfaces are critical interfaces where host-environment interactions occur, and the interplay between epithelial cells and immune components is essential for balancing tolerance and immunity. Disruptions to mucosal barrier integrity have profound consequences, contributing to the onset and progression of numerous diseases. Moreover, mucosal surfaces are key entry points for pathogens, including emerging viral threats, making a robust barrier indispensable for preventing infection. Despite the importance of this barrier, our understanding of how it is regulated and integrates signals from the microbiome to the immune cells is poorly understood.
This exciting opportunity aims to unravel the intricate interactions between immune cells and epithelial tissues, with a focus on understanding their roles in maintaining barrier integrity and immune homeostasis in mucosal environments such as the gut, lungs, and skin. This project will investigate how epithelial cells communicate with innate and adaptive immune cells to modulate responses to microbial, dietary, and environmental stimuli.
Utilizing cutting-edge approaches including advanced imaging, organoid co-culture systems, multiomics, and animal models, the candidate will uncover molecular mechanisms that underpin immune-epithelial cross-talk. The findings will unravel new knowledge that sets the foundation for the development of new strategies for diseases such as inflammatory bowel disease, asthma, and other epithelial barrier disorders.
The Belz Laboratory
The successful candidate will join a dynamic and interdisciplinary research team in a supportive academic environment. Our team is composed of highly collaborative passionate post-doctoral scientists, research assistants and PhD students with diverse backgrounds. We have expertise in state-of the art imaging, multi-dimensional flow cytometry and mucosal immunology. We provide a unique, collaborative environment and opportunity to develop diverse skill-sets and make impactful discoveries.
Frazer Institute at the University of Queensland
The Frazer Institute at the University of Queensland offers a dynamic and collaborative research environment dedicated to advancing biomedical innovation. Situated in Brisbane, a vibrant and rapidly growing hub for science and technology, the Institute provides access to world-class facilities and resources in a stunning subtropical setting.
As a leading research centre, the Frazer Institute fosters interdisciplinary collaboration, bringing together experts in immunology, molecular biology, and translational medicine. Its strategic partnerships with hospitals, biotech industries, and global research networks enable researchers to translate discoveries into real-world applications.
The Institute is equipped with state-of-the-art technologies, including single-cell genomics, high-resolution imaging, organoid platforms, and advanced proteomics. These cutting-edge tools empower researchers to explore complex biological questions with unprecedented precision.
With its emphasis on mentorship, innovation, and impact-driven research, the Frazer Institute offers exceptional opportunities for scientists aiming to contribute to transformative discoveries in health and medicine.
The Frazer Institute is committed to diversity and equal opportunity and the development of emerging researchers at the highest level.
Supervision history
Current supervision
-
Doctor Philosophy
Deciphering the protective program of innate and adaptive cells in pathogen infection
Principal Advisor
Other advisors: Associate Professor Timothy Wells
-
Doctor Philosophy
High Mobility Group Box Family Member TOX2 in Innate Lymphoid Cell Development and Maintenance
Principal Advisor
Other advisors: Associate Professor Timothy Wells
-
Doctor Philosophy
The role of innate cells in shaping the tumour environment.
Principal Advisor
Other advisors: Associate Professor Fernando Guimaraes, Dr M. Zeeshan Chaudhry
-
Doctor Philosophy
Understanding development of an mRNA vaccine to prevent Group A Streptococcus pharyngeal infection
Principal Advisor
Other advisors: Professor Mark Walker
-
Doctor Philosophy
Innate lymphoid cells in tumour control
Principal Advisor
-
Doctor Philosophy
Immune Regulation of Lung Injury: Pathways to Repair, Restoration and Fibrosis
Principal Advisor
Other advisors: Professor Dan Chambers
-
Doctor Philosophy
Understanding development of an mRNA vaccine to prevent Group A Streptococcus pharyngeal infection
Principal Advisor
Other advisors: Professor Mark Walker
-
Doctor Philosophy
Studying the tumour immune microenvironment in cutaneous squamous cell carcinoma
Principal Advisor
Other advisors: Associate Professor Arutha Kulasinghe
-
Doctor Philosophy
Understanding Key Epithelial Cells Following Lung Infection
Principal Advisor
Other advisors: Associate Professor Fernando Guimaraes
-
Doctor Philosophy
Understanding Key Epithelial Cells Following Lung Infection
Principal Advisor
Other advisors: Associate Professor Fernando Guimaraes
-
Doctor Philosophy
Preclinical refinement of a UQ-Moderna vaccine developed to prevent StrepA infection
Associate Advisor
Other advisors: Dr Nichaela Harbison-Price, Professor Mark Walker
-
Doctor Philosophy
Development of natural killer cells with enhanced tumoricidal functions using CRISPR homology-directed repair-mediated gene editing
Associate Advisor
Other advisors: Dr Allie Lam, Associate Professor Fernando Guimaraes
-
Doctor Philosophy
Understanding immune diversity in skin inflammation
Associate Advisor
Other advisors: Professor Kiarash Khosrotehrani, Dr Snehlata Kumari
-
Doctor Philosophy
The Ins and Outs of Endocytosis inhibition: Providing diverse opportunities for treatment of incurable cancers
Associate Advisor
Other advisors: Dr Shannon Joseph, Professor Fiona Simpson
Completed supervision
Media
Enquiries
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