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Professor Gabrielle Belz
Professor

Gabrielle Belz

Email: 

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

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

295 works between 1981 and 2025

21 - 40 of 295 works

2023

Journal Article

Innate lymphoid cells: potential targets for cancer therapeutics

Ng, Chun Ki and Belz, Gabrielle T. (2023). Innate lymphoid cells: potential targets for cancer therapeutics. Trends in Cancer, 9 (2), 158-171. doi: 10.1016/j.trecan.2022.10.007

Innate lymphoid cells: potential targets for cancer therapeutics

2023

Journal Article

IFI27 transcription is an early predictor for COVID-19 outcomes, a multi-cohort observational study

Shojaei, Maryam, Shamshirian, Amir, Monkman, James, Grice, Laura, Tran, Minh, Tan, Chin Wee, Teo, Siok Min, Rodrigues Rossi, Gustavo, McCulloch, Timothy R., Nalos, Marek, Raei, Maedeh, Razavi, Alireza, Ghasemian, Roya, Gheibi, Mobina, Roozbeh, Fatemeh, Sly, Peter D., Spann, Kirsten M., Chew, Keng Yih, Zhu, Yanshan, Xia, Yao, Wells, Timothy J., Senegaglia, Alexandra Cristina, Kuniyoshi, Carmen Lúcia, Franck, Claudio Luciano, dos Santos, Anna Flavia Ribeiro, Noronha, Lucia de, Motamen, Sepideh, Valadan, Reza, Amjadi, Omolbanin ... Tang, Benjamin (2023). IFI27 transcription is an early predictor for COVID-19 outcomes, a multi-cohort observational study. Frontiers in Immunology, 13 1060438, 1-14. doi: 10.3389/fimmu.2022.1060438

IFI27 transcription is an early predictor for COVID-19 outcomes, a multi-cohort observational study

2023

Journal Article

Author Correction: CIS is a potent checkpoint in NK cell–mediated tumor immunity (Nature Immunology, (2016), 17, 7, (816-824), 10.1038/ni.3470)

Delconte, Rebecca B., Kolesnik, Tatiana B., Dagley, Laura F., Rautela, Jai, Shi, Wei, Putz, Eva M., Stannard, Kimberley, Zhang, Jian-Guo, Teh, Charis, Firth, Matt, Ushiki, Takashi, Andoniou, Christopher E., Degli-Esposti, Mariapia A., Sharp, Phillip P., Sanvitale, Caroline E., Infusini, Giuseppe, Liau, Nicholas P. D., Linossi, Edmond M., Burns, Christopher J., Carotta, Sebastian, Gray, Daniel H. D., Seillet, Cyril, Hutchinson, Dana S., Belz, Gabrielle T., Webb, Andrew I., Alexander, Warren S., Li, Shawn S., Bullock, Alex N., Babon, Jeffrey J. ... Huntington, Nicholas D. (2023). Author Correction: CIS is a potent checkpoint in NK cell–mediated tumor immunity (Nature Immunology, (2016), 17, 7, (816-824), 10.1038/ni.3470). Nature Immunology, 25 (2), 371-372. doi: 10.1038/s41590-023-01714-8

Author Correction: CIS is a potent checkpoint in NK cell–mediated tumor immunity (Nature Immunology, (2016), 17, 7, (816-824), 10.1038/ni.3470)

2023

Journal Article

Gutsy sensations modulate intestinal disease

Cao, Wang and Belz, Gabrielle (2023). Gutsy sensations modulate intestinal disease. Trends in Immunology, 44 (1), 1-3. doi: 10.1016/j.it.2022.11.007

Gutsy sensations modulate intestinal disease

2022

Conference Publication

Deep single-cell, proteogenomic insights from SARS-CoV-2 infected lung tissues

Kulasinghe, Arutha, Tan, Chin Wee, Liu, Ning, Monkman, James, Killingbeck, Emily, Kim, Youngmi, Pan, Liuliu, Blick, Tony, Bhuva, Dharmesh, Feher, Kristen, Leon, Michael, Gregory, Mark, Short, Kirsty, Guimaraes, Fernando, Rhodes, Michael, Belz, Gabrielle and Davis, Melissa (2022). Deep single-cell, proteogenomic insights from SARS-CoV-2 infected lung tissues. SITC 37th Annual Meeting (SITC 2022), Boston, MA USA, 8-12 November 2022. London, United Kingdom: BMJ Publishing Group. doi: 10.1136/jitc-2022-sitc2022.0923

Deep single-cell, proteogenomic insights from SARS-CoV-2 infected lung tissues

2022

Conference Publication

High-dimensional spatial phenotyping of cutaneous squamous cell carcinoma from immune-competent and immunocompromised patients

Kulasinghe, Arutha, Jhaveri, Niyati, Klymyshyn, Dmytro, Cheikh, Bassem Ben, Ladwa, Rahul, Liu, Howard, Cooper, Caroline, Belz, Gabrielle, Porceddu, Sandro and Braubach, Oliver (2022). High-dimensional spatial phenotyping of cutaneous squamous cell carcinoma from immune-competent and immunocompromised patients. SITC 37th Annual Meeting (SITC 2022), Boston, MA United States, 8–12 November 2022. London, United Kingdom: BMJ Group. doi: 10.1136/jitc-2022-sitc2022.0079

High-dimensional spatial phenotyping of cutaneous squamous cell carcinoma from immune-competent and immunocompromised patients

2022

Journal Article

Metabolic features of innate lymphoid cells

Yu, Huiyang, Jacquelot, Nicolas and Belz, Gabrielle T. (2022). Metabolic features of innate lymphoid cells. Journal of Experimental Medicine, 219 (11) e20221140. doi: 10.1084/jem.20221140

Metabolic features of innate lymphoid cells

2022

Journal Article

A protocol to isolate bone marrow innate lymphoid cells for alymphoid mouse reconstitution

Jacquelot, Nicolas, Huang, Qiutong, Belz, Gabrielle T. and Seillet, Cyril (2022). A protocol to isolate bone marrow innate lymphoid cells for alymphoid mouse reconstitution. STAR Protocols, 3 (3) 101534, 1-19. doi: 10.1016/j.xpro.2022.101534

A protocol to isolate bone marrow innate lymphoid cells for alymphoid mouse reconstitution

2022

Journal Article

Transcriptomic profiling of cardiac tissues from SARS‐CoV ‐2 patients identifies DNA damage

Kulasinghe, Arutha, Liu, Ning, Tan, Chin Wee, Monkman, James, Sinclair, Jane E., Bhuva, Dharmesh D., Godbolt, David, Pan, Liuliu, Nam, Andy, Sadeghirad, Habib, Sato, Kei, Bassi, Gianluigi Li, O'Byrne, Ken, Hartmann, Camila, Miggiolaro, Anna Flavia Ribeiro dos Santos, Marques, Gustavo Lenci, Moura, Lidia Zytynski, Richard, Derek, Adams, Mark, Noronha, Lucia de, Baena, Cristina Pellegrino, Suen, Jacky Y., Arora, Rakesh, Belz, Gabrielle T., Short, Kirsty R., Davis, Melissa J., Souza‐Fonseca Guimaraes, Fernando and Fraser, John F. (2022). Transcriptomic profiling of cardiac tissues from SARS‐CoV ‐2 patients identifies DNA damage. Immunology, 168 (3), 403-419. doi: 10.1111/imm.13577

Transcriptomic profiling of cardiac tissues from SARS‐CoV ‐2 patients identifies DNA damage

2022

Journal Article

ZBTB46 in ILC3: shared transcriptional infrastructure defines gut-protective capabilities

Curio, Sophie and Belz, Gabrielle T. (2022). ZBTB46 in ILC3: shared transcriptional infrastructure defines gut-protective capabilities. Trends in Immunology, 43 (9), 690-692. doi: 10.1016/j.it.2022.07.008

ZBTB46 in ILC3: shared transcriptional infrastructure defines gut-protective capabilities

2022

Journal Article

CIS and TGF ‐β regulatory pathways influence immunity to bacterial infection

McCulloch, Timothy R., Rossi, Gustavo R., Schreuder, Jaring, Belz, Gabrielle T., Wells, Timothy J. and Souza‐Fonseca‐Guimaraes, Fernando (2022). CIS and TGF ‐β regulatory pathways influence immunity to bacterial infection. Immunology, 167 (1), 54-63. doi: 10.1111/imm.13516

CIS and TGF ‐β regulatory pathways influence immunity to bacterial infection

2022

Journal Article

Influenza vaccination induces autoimmunity against orexinergic neurons in a mouse model for narcolepsy

Bernard-Valnet, Raphael, Frieser, David, Nguyen, Xuan-Hung, Khajavi, Leila, Queriault, Clemence, Arthaud, Sebastien, Melzi, Silvia, Fusade-Boyer, Maxime, Masson, Frederick, Zytnicki, Matthias, Saoudi, Abdelhadi, Dauvilliers, Yves, Peyron, Christelle, Bauer, Jan and Liblau, Roland S. (2022). Influenza vaccination induces autoimmunity against orexinergic neurons in a mouse model for narcolepsy. Brain, 145 (6), 2018-2030. doi: 10.1093/brain/awab455

Influenza vaccination induces autoimmunity against orexinergic neurons in a mouse model for narcolepsy

2022

Journal Article

Caspase-8 has dual roles in regulatory T cell homeostasis balancing immunity to infection and collateral inflammatory damage

Teh, Charis E., Preston, Simon P., Robbins, Alissa K., Stutz, Michael D., Cooney, James, Clark, Michelle P., Policheni, Antonia N., Allison, Cody C., Mackiewicz, Liana, Arandjelovic, Philip, Ebert, Gregor, Doerflinger, Marcel, Tan, Tania, Rankin, Lucille C., Teh, Peggy P., Belz, Gabrielle T., Kallies, Axel, Strasser, Andreas, Pellegrini, Marc and Gray, Daniel H D (2022). Caspase-8 has dual roles in regulatory T cell homeostasis balancing immunity to infection and collateral inflammatory damage. Science Immunology, 7 (69) eabn8041. doi: 10.1126/sciimmunol.abn8041

Caspase-8 has dual roles in regulatory T cell homeostasis balancing immunity to infection and collateral inflammatory damage

2022

Journal Article

Innate lymphoid cells and cancer

Jacquelot, Nicolas, Seillet, Cyril, Vivier, Eric and Belz, Gabrielle T. (2022). Innate lymphoid cells and cancer. Nature Immunology, 23 (3), 371-379. doi: 10.1038/s41590-022-01127-z

Innate lymphoid cells and cancer

2022

Journal Article

A diverse fibroblastic stromal cell landscape in the spleen directs tissue homeostasis and immunity

Alexandre, Yannick O., Schienstock, Dominik, Lee, Hyun Jae, Gandolfo, Luke C., Williams, Cameron G., Devi, Sapna, Pal, Bhupinder, Groom, Joanna R., Cao, Wang, Christo, Susan N., Gordon, Claire L., Starkey, Graham, D’Costa, Rohit, Mackay, Laura K., Haque, Ashraful, Ludewig, Burkhard, Belz, Gabrielle T. and Mueller, Scott N. (2022). A diverse fibroblastic stromal cell landscape in the spleen directs tissue homeostasis and immunity. Science Immunology, 7 (67) eabj0641, eabj0641. doi: 10.1126/sciimmunol.abj0641

A diverse fibroblastic stromal cell landscape in the spleen directs tissue homeostasis and immunity

2022

Journal Article

Profiling of lung SARS-CoV-2 and influenza virus infection dissects virus-specific host responses and gene signatures

Kulasinghe, Arutha, Tan, Chin Wee, dos Santos Miggiolaro, Anna Flavia Ribeiro, Monkman, James, SadeghiRad, Habib, Bhuva, Dharmesh D., da Silva Motta Junior, Jarbas, Vaz de Paula, Caroline Busatta, Nagashima, Seigo, Baena, Cristina Pellegrino, Souza-Fonseca-Guimaraes, Paulo, de Noronha, Lucia, McCulloch, Timothy, Rodrigues Rossi, Gustavo, Cooper, Caroline, Tang, Benjamin, Short, Kirsty R., Davis, Melissa J., Souza-Fonseca-Guimaraes, Fernando, Belz, Gabrielle T. and O'Byrne, Ken (2022). Profiling of lung SARS-CoV-2 and influenza virus infection dissects virus-specific host responses and gene signatures. European Respiratory Journal, 59 (6) 2101881, 1-19. doi: 10.1183/13993003.01881-2021

Profiling of lung SARS-CoV-2 and influenza virus infection dissects virus-specific host responses and gene signatures

2022

Journal Article

The unique role of innate lymphoid cells in cancer and the hepatic microenvironment

Curio, Sophie and Belz, Gabrielle T. (2022). The unique role of innate lymphoid cells in cancer and the hepatic microenvironment. Cellular and Molecular Immunology, 19 (9), 1012-1029. doi: 10.1038/s41423-022-00901-1

The unique role of innate lymphoid cells in cancer and the hepatic microenvironment

2021

Other Outputs

IFI27 transcription is an early predictor for COVID-19 outcomes; a multi-cohort observational study

Shojaei, Maryam, Shamshirian, Amir, Monkman, James, Grice, Laura, Tran, Minh, Tan, Chin Wee, Rossi, Gustavo Rodrigues, McCulloch, Timothy R., Nalos, Marek, Chew, Keng Yih, Zhu, Yanshan, Xia, Yao, Wells, Timothy J., Senegaglia, Alexandra Cristina, Rebelatto, Carmen Lúcia Kuniyoshi, Franck, Claudio Luciano, dos Santos, Anna Flavia Ribeiro, de Noronha, Lucia, Motamen, Sepideh, Valadan, Reza, Amjadi, Omolbanin, Gogna, Rajan, Madan, Esha, Alizadeh-Navaei, Reza, Lamperti, Liliana, Zuñiga, Felipe, Nova-Lamperti, Estefania, Labarca, Gonzalo, Knippenberg, Ben ... Tang, Benjamin (2021). IFI27 transcription is an early predictor for COVID-19 outcomes; a multi-cohort observational study. doi: 10.1101/2021.10.29.21265555

IFI27 transcription is an early predictor for COVID-19 outcomes; a multi-cohort observational study

2021

Journal Article

Metastasis-entrained eosinophils enhance lymphocyte-mediated anti-tumor immunity

Grisaru-Tal, Sharon, Dulberg, Shai, Beck, Lir, Zhang, Chunyan, Itan, Michal, Hediyeh-zadeh, Soroor, Caldwell, Julie, Rozenberg, Perri, Dolitzky, Avishay, Avlas, Shmuel, Hazut, Inbal, Gordon, Yaara, Shani, Ophir, Tsuriel, Shlomo, Gerlic, Motti, Erez, Neta, Jacquelot, Nicolas, Belz, Gabrielle, Rothenberg, Marc E, Davis, Melissa J, Yu, Hua, Geiger, Tamar, Madi, Asaf and Munitz, Ariel (2021). Metastasis-entrained eosinophils enhance lymphocyte-mediated anti-tumor immunity. Cancer Research, 81 (21), 5555-5571. doi: 10.1158/0008-5472.can-21-0839

Metastasis-entrained eosinophils enhance lymphocyte-mediated anti-tumor immunity

2021

Journal Article

Discrete tissue microenvironments instruct diversity in resident memory T cell function and plasticity

Christo, Susan N., Evrard, Maximilien, Park, Simone L., Gandolfo, Luke C., Burn, Thomas N., Fonseca, Raissa, Newman, Dane M., Alexandre, Yannick O., Collins, Nicholas, Zamudio, Natasha M., Souza-Fonseca-Guimaraes, Fernando, Pellicci, Daniel G., Chisanga, David, Shi, Wei, Bartholin, Laurent, Belz, Gabrielle T., Huntington, Nicholas D., Lucas, Andrew, Lucas, Michaela, Mueller, Scott N., Heath, William R., Ginhoux, Florent, Speed, Terence P., Carbone, Francis R., Kallies, Axel and Mackay, Laura K. (2021). Discrete tissue microenvironments instruct diversity in resident memory T cell function and plasticity. Nature Immunology, 22 (9), 1140-1151. doi: 10.1038/s41590-021-01004-1

Discrete tissue microenvironments instruct diversity in resident memory T cell function and plasticity

Funding

Current funding

  • 2025 - 2029
    Unravelling immune signalling networks that protect vertebrates from attack
    ARC Australian Laureate Fellowships
    Open grant
  • 2024 - 2028
    METASPATIAL Study: Metabolic Spatial Analysis of Lung Cancer Study
    NHMRC MRFF EMCR - Early to Mid-Career Researchers
    Open grant
  • 2024 - 2026
    From Pixels to Prognosis: Harnessing single-cell spatial analysis to predict and improve immunotherapy response in lung cancer
    Cure Cancer Early Career Research Grants
    Open grant
  • 2024 - 2026
    Preclinical refinement of a UQ-Moderna vaccine developed to prevent StrepA infection
    NHMRC Development Grant
    Open grant
  • 2024 - 2025
    Screening experimental adjuvants in non-human primates for improved Group A Streptococcus (GAS) vaccine efficacy
    The University of Queensland in America, Inc
    Open grant
  • 2023 - 2026
    Regulation of lung immune-epithelial networks sensing environmental change
    ARC Discovery Projects
    Open grant
  • 2023 - 2028
    Building the next mRNA vaccines and therapies
    MRFF - National Critical Infrastructure Initiative
    Open grant
  • 2023 - 2026
    Personalising Innate-immunotherapy for Superior Treatment Outcomes with Large anticancer applicability (PISTOL)
    NHMRC MRFF EMCR - Early to Mid-Career Researchers
    Open grant
  • 2022 - 2026
    Harnessing immune cell programs to drive immune protection
    NHMRC Investigator Grants
    Open grant

Past funding

  • 2022 - 2024
    Determining Causative Mechanisms of Hidradenitis Suppurativa (TRI LINC grant led by MSHHS)
    Metro South Hospital and Health Service
    Open grant
  • 2022 - 2024
    LUNG PREDICT Study
    Cancer Australia
    Open grant
  • 2022
    Generating neuroprotective IgA through microbiome-epithelial interactions
    MS Research Australia Project Grant
    Open grant
  • 2022 - 2024
    Type 2 innate lymphoid cells orchestrate anti-melanoma responses.
    Cancer Council NSW Project Grant
    Open grant
  • 2021 - 2022
    Cutaneous squamous cell carcinoma and tumour MICroenvironment Multiplex Spatial Profiling - cMIC STUDY (PA Research Foundation Award administered by MSHHS)
    Metro South Hospital and Health Service
    Open grant
  • 2021 - 2023
    Coordinating neuroimmune sensory networks in health and disease
    NHMRC IDEAS Grants
    Open grant
  • 2020 - 2023
    New guardians of the mucosa: Molecular characterisation of M cell biology (ARC Discovery Project administered by UTS)
    University of Technology Sydney
    Open grant
  • 2020 - 2022
    Delineating immune circuits for innate and adaptive immune protection
    NHMRC Research Fellowship
    Open grant
  • 2019 - 2023
    The recirculation of myeloid dendritic cells
    ARC Discovery Projects
    Open grant
  • 2019 - 2021
    Understanding the circadian regulation of the innate lymphoid cells (NHMRC Project Grant administered by WEHI)
    Walter & Eliza Hall Institute of Medical Research (WEHI)
    Open grant

Supervision

Availability

Professor Gabrielle Belz is:
Available for supervision

Before you email them, read our advice on how to contact a supervisor.

Available projects

  • 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

  • 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

Completed supervision

Media

Enquiries

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