
Overview
Background
Professor Kate Schroder heads the Inflammasome Laboratory and is Director of the Centre for Inflammation and Disease Research at the Institute for Molecular Bioscience (IMB), University of Queensland, as an NHMRC Leadership Fellow. Kate’s graduate studies defined novel macrophage activation mechanisms and her subsequent postdoctoral research identified surprising inter-species divergence in the inflammatory programs of human versus mouse macrophages. As an NHMRC CJ Martin Fellow in Switzerland, Kate trained with the pioneer of inflammasome biology, Jürg Tschopp. The IMB Inflammasome Laboratory, which Kate heads, investigates the molecular mechanisms governing inflammasome activity and caspase activation, the cellular mediators of inflammasome-dependent inflammation, and mechanisms of inflammasome inhibition by cellular pathways and small molecule inhibitors.
Kate is a co-inventor on patents for small molecule inhibitors of the NLRP3 inflammasome, currently under commercialisation by Inflazome Ltd. Inflazome Ltd was recently acquired by Roche in a landmark deal – one of the largest in Australian and Irish biotech history. The acquisition gives Roche full rights to Inflazome’s portfolio of inflammasome inhibitors. Two of the company’s drug candidates are in clinical trials for the treatment of debilitating conditions such as cardiovascular disease, arthritis and neurodegenerative diseases such as Parkinson’s, Alzheimer’s and motor neuron disease.
Kate has authored more than 140 publications, featuring in journals such as Science, Cell, Nature Genetics, Nature Medicine, Nature Chemical Biology, Journal of Experimental Medicine and PNAS USA, and her work has been cited more than 35,000 times. Kate is an Editorial Board Member for international journals including Science Signaling, Clinical and Translational Immunology and Cell Death Disease. She is the recipient of the 2022 Women in Technology Excellence in Science Award, 2020 Nancy Mills Award for Women in Science, 2019 ANZSCDB Emerging Leader Award, 2019 Merck Research Medal, 2014 Milstein Young Investigator Award, 2013 Tall Poppy Award, 2012 Gordon Ada Career Award, 2010 QLD Premier’s Postdoctoral Award, and the 2008 Society for Leukocyte Biology’s Dolph Adams Award.
INFLAMMASOME LABORATORY RESEARCH
During injury or infection, our body’s immune system protects us by launching inflammation. But uncontrolled inflammation drives diseases such as gout, diabetes, neurodegenerative disease and cancer. The Inflammasome Lab is defining the molecular and cellular processes of inflammation. We seek to unravel the secrets of inflammasomes – protein complexes at the heart of inflammation and disease – to allow for new therapies to fight human diseases.
The Inflammasome Laboratory integrates molecular and cell biology approaches with in vivo studies to gain a holistic understanding of inflammasome function during infection, and inflammasome dysfunction in human inflammatory disease. Current research interests include the molecular mechanisms governing inflammasome activity and caspase activation, the cellular mediators of inflammasome-dependent inflammation, and inflammasome suppression by autophagy and small molecule inhibitors.
Availability
- Professor Kate Schroder is:
- Available for supervision
- Media expert
Fields of research
Qualifications
- Bachelor (Honours) of Science (Advanced), The University of Queensland
- Doctor of Philosophy, The University of Queensland
Research impacts
Our research focuses on understanding how immune cells launch healthy inflammation to fight infection and unhealthy inflammation to promote disease. By understanding exactly how the body fights infection, we can help identify new drug targets or vaccines to combat infectious disease, which causes 13 million deaths globally each year. By understanding how unhealthy inflammation is initiated, we may also be able to design new strategies for the treatment of common diseases such as cancer, gout and diabetes.
Works
Search Professor Kate Schroder’s works on UQ eSpace
2016
Journal Article
Familial auto inflammation with neutrophilic dermatosis reveals a novel regulatory mechanism of pyrin activation
Masters, Seth L., Lagou, Vasiliki, Jéru, Isabelle, Baker, Paul J., Van Eyck, Lien, Parry, David A., Lawless, Dylan, De Nardo, Dominic, Garcia-Perez, Josselyn E., Dagley, Laura F., Holley, Caroline L., Dooley, James, Moghaddas, Fiona, Pasciuto, Emanuela, Jeandel, Pierre-Yves, Sciot, Raf, Lyras, Dena, Webb, Andrew I., Nicholson, Sandra E., De Somer, Lien, van Nieuwenhove, Erika, Ruuth-Praz, Julia, Copin, Bruno, Cochet, Emmanuelle, Medlej-Hashim, Myrna, Megarbane, Andre, Schroder, Kate, Savic, Sinisa, Goris, An ... Liston, Adrian (2016). Familial auto inflammation with neutrophilic dermatosis reveals a novel regulatory mechanism of pyrin activation. Science Translational Medicine, 8 (332) 332ra45, 1-9. doi: 10.1126/scitranslmed.aaf1471
2016
Journal Article
Sterile signals generate weaker and delayed macrophage NLRP3 inflammasome responses relative to microbial signals
Bezbradica, Jelena S., Coll, Rebecca C. and Schroder, Kate (2016). Sterile signals generate weaker and delayed macrophage NLRP3 inflammasome responses relative to microbial signals. Cellular and Molecular Immunology, 1-9. doi: 10.1038/cmi.2016.11
2016
Journal Article
Salmonella employs multiple mechanisms to subvert the TLR-inducible zinc-mediated antimicrobial response of human macrophages
Kapetanovic, Ronan, Bokil, Nilesh J., Achard, Maud E. S., Ong, Cheryl-lynn Y, Peters, Kate M., Stocks, Claudia J., Phan, Minh-Duy, Monteleone, Mercedes, Schroder, Kate, Irvine, Katharine M., Saunders, Bernadette M., Walker, Mark J., Stacey, Katryn J., McEwan, Alastair G., Schembri, Mark A. and Sweet, Matthew J. (2016). Salmonella employs multiple mechanisms to subvert the TLR-inducible zinc-mediated antimicrobial response of human macrophages. The FASEB Journal, 30 (5), 1901-1912. doi: 10.1096/fj.201500061
2016
Journal Article
The E3 ubiquitin ligase RNF144B is LPS-inducible in human but not mouse macrophages, and promotes inducible IL-1β expression
Ariffin, Juliana K., Kapetanovic, Ronan, Schaale, Kolja, Gatica-Andrades, Marcela, Blumenthal, Antje, Schroder, Kate and Sweet, Matthew J. (2016). The E3 ubiquitin ligase RNF144B is LPS-inducible in human but not mouse macrophages, and promotes inducible IL-1β expression. Journal of Leukocyte Biology, 100 (1), 155-161. doi: 10.1189/jlb.2AB0815-339R
2016
Journal Article
NLRP12 is a neutrophil-specific, negative regulator of in vitro cell migration but does not modulate LPS- or infection-induced NF-κB or ERK signalling
Zamoshnikova, Alina, Grob, Christina J., Schuster, Steffen, Chen, Kaiwen W., Wilson, Anne, Tacchini-Cottier, Fabienne and Schroder, Kate (2016). NLRP12 is a neutrophil-specific, negative regulator of in vitro cell migration but does not modulate LPS- or infection-induced NF-κB or ERK signalling. Immunobiology, 221 (2), 341-346. doi: 10.1016/j.imbio.2015.10.001
2016
Book Chapter
Assessment of inflammasome formation by flow cytometry
Sester, David P., Zamoshnikova, Alina, Thygesen, Sara J., Vajjhala, Parimala R., Cridland, Simon O., Schroder, Kate and Stacey, Katryn J. (2016). Assessment of inflammasome formation by flow cytometry. Current protocols in immunology. (pp. 14.40.1-14.40.29) edited by Coligan, John E., Bierer, Barbara, Margulies, David H., Shevach, Ethan M. and Strober, Warren. Hoboken, NJ United States: John Wiley & Sons. doi: 10.1002/cpim.13
2016
Journal Article
Strain- and host species-specific inflammasome activation, IL-1β release, and cell death in macrophages infected with uropathogenic Escherichia coli.
Schaale, K., Peters, K. M., Murthy, A. M., Fritzsche, A. K., Phan, M.-D., Totsika, M., Robertson, A. A. B., Nichols, K. B., Cooper, M. A., Stacey, K. J., Ulett, G. C., Schroder, K., Schembri, M. A. and Sweet, M. J. (2016). Strain- and host species-specific inflammasome activation, IL-1β release, and cell death in macrophages infected with uropathogenic Escherichia coli.. Mucosal Immunology, 9 (1), 124-136. doi: 10.1038/mi.2015.44
2016
Conference Publication
Molecular arrangement and activation of procaspases-1 and-8 at inflammasomes
Vajjhala, P., Lu, A., Brown, D., Sagulenko, V, Schroder, K., Stow, J., Wu, H. and Stacey, K. (2016). Molecular arrangement and activation of procaspases-1 and-8 at inflammasomes. ICI 2016 International Congress of Immunology, Melbourne, Australia, 21-26 August 2016. Weinheim, Germany: Wiley.
2015
Journal Article
The inflammasome adaptor ASC induces procaspase-8 death effector domain filaments
Vajjhala, Parimala R., Lu, Alvin, Brown, Darren L., Pang, Siew Wai, Sagulenko, Vitaliya, Sester, David P., Cridland, Simon O., Hill, Justine M., Schroder, Kate, Stow, Jennifer L., Wu, Hao and Stacey, Katryn J. (2015). The inflammasome adaptor ASC induces procaspase-8 death effector domain filaments. Journal of Biological Chemistry, 290 (49), 29217-29230. doi: 10.1074/jbc.M115.687731
2015
Journal Article
TRIM-mediated precision autophagy targets cytoplasmic regulators of innate immunity
Kimura, Tomonori, Jain, Ashish, Choi, Seong Won, Mandell, Michael A., Schroder, Kate, Johansen, Terje and Deretic, Vojo (2015). TRIM-mediated precision autophagy targets cytoplasmic regulators of innate immunity. Journal of Cell Biology, 210 (6), 973-989. doi: 10.1083/jcb.201503023
2015
Journal Article
Metabolic gene expression changes in astrocytes in Multiple Sclerosis cerebral cortex are indicative of immune-mediated signaling
Zeis, T., Allaman, I., Gentner, M., Schroder, K., Tschopp, J., Magistretti, P. J. and Schaeren-Wiemers, N. (2015). Metabolic gene expression changes in astrocytes in Multiple Sclerosis cerebral cortex are indicative of immune-mediated signaling. Brain, Behavior, and Immunity, 48, 313-325. doi: 10.1016/j.bbi.2015.04.013
2015
Journal Article
Mechanisms of unconventional secretion of IL-1 family cytokines
Monteleone, Mercedes, Stow, Jennifer L. and Schroder, Kate (2015). Mechanisms of unconventional secretion of IL-1 family cytokines. Cytokine, 74 (2), 213-218. doi: 10.1016/j.cyto.2015.03.022
2015
Journal Article
Deficient NLRP3 and AIM2 Inflammasome Function in Autoimmune NZB Mice.
Sester, David P., Sagulenko, Vitaliya, Thygesen, Sara J., Cridland, Jasmyn A., Loi, Yen Siew, Cridland, Simon O., Masters, Seth L., Genske, Ulrich, Hornung, Veit, Andoniou, Christopher E., Sweet, Matthew J., Degli-Esposti, Mariapia A., Schroder, Kate and Stacey, Katryn J. (2015). Deficient NLRP3 and AIM2 Inflammasome Function in Autoimmune NZB Mice.. Journal of Immunology, 195 (3), 1233-1241. doi: 10.4049/jimmunol.1402859
2015
Conference Publication
The adaptor protein ASC controls transplantation outcomes independently of the inflammasome
Cheong, Melody, Gartlan, Kate, Tey, Siok-Keen, Kuns, Rachel, Lor, Mary, Lineburg, Katie, Tea, Bianca, Shi, Wei, Raju, Jyothy, Zhang, Ping, Varelias, Antiopi, Leveque-El Mouttie, Lucie, Olver, Stuart, Bunting, Mark, Lane, Steven, Boyle, Glen, Ting, Jenny, Schroder, Kate, Engwerda, Christian, Khanna, Kum Kum, Smyth, Mark, MacDonald, Kelli, Koyama, Motoko and Hill, Geoffrey (2015). The adaptor protein ASC controls transplantation outcomes independently of the inflammasome. Annual Meeting of the American-Association-of-Immunologists (IMMUNOLOGY), New Orleans La, May 08-12, 2015. BETHESDA: AMER ASSOC IMMUNOLOGISTS.
2015
Journal Article
A novel flow cytometric method to assess inflammasome formation
Sester, David P., Thygesen, Sara J., Sagulenko, Vitaliya, Vajjhala, Parimala R., Cridland, Jasmyn A., Vitak, Nazarii, Chen, Kaiwen W., Osborne, Geoffrey W., Schroder, Kate and Katryn J. Stacey (2015). A novel flow cytometric method to assess inflammasome formation. The Journal of Immunology, 194 (1), 455-462. doi: 10.4049/jimmunol.1401110
2015
Journal Article
Burn the house, save the day: pyroptosis in pathogen restriction
Boucher, Dave, Chen, Kaiwen W. and Schroder, Kate (2015). Burn the house, save the day: pyroptosis in pathogen restriction. Inflammasome, 2 (1), 1-6. doi: 10.1515/infl-2015-0001
2014
Journal Article
Sphingomyelin phosphodiesterase Acid-like 3A (SMPDL3A) is a novel nucleotide phosphodiesterase regulated by cholesterol in human macrophages
Traini, Mathew, Quinn, Carmel M., Sandoval, Cecilia, Johansson, Erik, Schroder, Kate, Kockx, Maaike, Meikle, Peter J., Jessup, Wendy and Kritharides, Leonard (2014). Sphingomyelin phosphodiesterase Acid-like 3A (SMPDL3A) is a novel nucleotide phosphodiesterase regulated by cholesterol in human macrophages. Journal of Biological Chemistry, 289 (47), 32895-32913. doi: 10.1074/jbc.M114.612341
2014
Journal Article
TRAF6 is a nexus for TLR-STAT1 crosstalk
Bezbradica, Jelena S. and Schroder, Kate (2014). TRAF6 is a nexus for TLR-STAT1 crosstalk. Immunology and Cell Biology, 92 (9), 737-738. doi: 10.1038/icb.2014.71
2014
Journal Article
Rab8a interacts directly with PI3Kγ to modulate TLR4-driven PI3K and mTOR signalling
Luo, Lin, Wall, Adam A., Yeo, Jeremy C., Condon, Nicholas D., Norwood, Suzanne J., Schoenwaelder, Simone, Chen, Kaiwen W., Jackson, Shaun, Jenkins, Brendan J., Hartland, Elizabeth L., Schroder, Kate, Collins, Brett M., Sweet, Matthew J. and Stow, Jennifer L. (2014). Rab8a interacts directly with PI3Kγ to modulate TLR4-driven PI3K and mTOR signalling. Nature Communications, 5 (1) 4407, 4407.1-4407.13. doi: 10.1038/ncomms5407
2014
Conference Publication
A novel approach to investigate the assembly of the NOD-like receptor inflammasomes
Giles, Nichole, Sierecki, Emma, Polinkovsky, Mark, Schroder, Kate, Alexandrov, Kirill and Gambin, Yann (2014). A novel approach to investigate the assembly of the NOD-like receptor inflammasomes. Experimental Biology Meeting, San Diego Ca, 26-30 April 2014. Bethesda, MD United States: Federation of American Societies for Experimental Biology.
Funding
Current funding
Past funding
Supervision
Availability
- Professor Kate Schroder is:
- Available for supervision
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Available projects
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Student projects
Expressions of interest from prospective postgraduate students are welcome at any time. For information on future research higher degree projects, please email K.Schroder@imb.uq.edu.au with the following: (1) CV, including a summary of academic qualifications, work and research experience, and publication list; (2) studies report for undergraduate and honours degree(s); and (3) a letter of motivation outlining your research interests.
Supervision history
Current supervision
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Doctor Philosophy
Mechanisms of virus-induced NLRP1 Inflammasome Signalling
Principal Advisor
Other advisors: Dr Larisa Labzin
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Doctor Philosophy
Mechanisms of Inflammasome Assembly and Signalling
Principal Advisor
-
Doctor Philosophy
Inflammasome inhibition by molecular and cellular processes in fibrosis (e.g. systemic sclerosis)
Principal Advisor
Other advisors: Dr Sabrina Sofia Burgener
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Doctor Philosophy
Inflammasomes in tissue homeostasis and wound healing
Principal Advisor
Other advisors: Dr Sabrina Sofia Burgener
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Doctor Philosophy
Molecular pathways by which human epithelia and macrophages sense and respond to Influenza A virus infection.
Associate Advisor
Other advisors: Professor Kirsty Short, Dr Larisa Labzin
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Doctor Philosophy
Investigating how antibodies against Influenza A Virus modulate macrophage sensing and signalling pathways and outputs.
Associate Advisor
Other advisors: Professor Kirsty Short, Dr Larisa Labzin
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Doctor Philosophy
Molecular pathways by which human epithelia and macrophages sense and respond to Influenza A virus infection.
Associate Advisor
Other advisors: Professor Kirsty Short, Dr Larisa Labzin
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Doctor Philosophy
Discovery and Pharmacological Evaluation of Novel Analgesics for the Relief of Ross River Virus Induced Chronic Pain
Associate Advisor
Other advisors: Dr Andy Kuo, Emeritus Professor Maree Smith, Dr Mohammad Zafar Imam
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Doctor Philosophy
Inflammasome inhibitors in disease: Is there a therapeutic trade-off of compromised host defence?
Associate Advisor
Other advisors: Professor Avril Robertson, Dr Sabrina Sofia Burgener
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Doctor Philosophy
Molecular pathways by which human epithelia and macrophages sense and respond to Influenza A virus infection.
Associate Advisor
Other advisors: Professor Kirsty Short, Dr Larisa Labzin
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Doctor Philosophy
Studying the synergistic effects of streptococcal SLO and NADase on toxification of the host redox metabolism
Associate Advisor
Other advisors: Dr Stephan Brouwer, Professor Mark Walker
Completed supervision
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2024
Doctor Philosophy
Mitochondrial Dynamics and the NLRP3 Inflammasome
Principal Advisor
Other advisors: Professor Matt Sweet
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2023
Doctor Philosophy
Molecular mechanisms of inflammasome-driven Alzheimer's disease
Principal Advisor
Other advisors: Professor Jurgen Götz, Dr Sabrina Sofia Burgener
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2020
Doctor Philosophy
Molecular Mechanisms of Non-canonical Inflammasome Activity
Principal Advisor
Other advisors: Dr Ian Ross
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2018
Doctor Philosophy
Human-specific inflammasome signalling pathways in macrophages
Principal Advisor
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2015
Doctor Philosophy
Inflammasome function in neutrophils
Principal Advisor
Other advisors: Professor Matt Sweet
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2025
Doctor Philosophy
Molecular pathways by which human epithelia and macrophages sense and respond to Influenza A virus infection.
Associate Advisor
Other advisors: Professor Kirsty Short, Dr Larisa Labzin
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2023
Doctor Philosophy
Characterisation of the interaction of M1 Group A Streptococcus with the inflammasome pathway
Associate Advisor
Other advisors: Professor Mark Walker
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2020
Doctor Philosophy
Novel therapeutic targets for the treatment of vincristine induced peripheral neuropathy
Associate Advisor
Other advisors: Professor Irina Vetter
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2018
Doctor Philosophy
Inflammasomes and Autoimmunity
Associate Advisor
Other advisors: Professor Kate Stacey
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2015
Doctor Philosophy
Characterisation of Human Macrophage Functions in Innate Immunity
Associate Advisor
Other advisors: Professor Matt Sweet, Professor David Fairlie
Media
Enquiries
Contact Professor Kate Schroder directly for media enquiries about:
- Alzheimer's disease
- arthritis
- cancer
- candida
- caspase
- cell biology
- cytokine
- diabetes
- gout
- hereditary disease
- immune system
- inerluekin
- infection
- infectious disease
- inflammasome
- inflammation
- inflammatory disease
- innate immunity
- macrophage
- myeloid
- neutrophil
- nod-like receptor
- pyroptosis
- salmonella
- toll-like receptor
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