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Professor Kate Schroder
Professor

Kate Schroder

Email: 
Phone: 
+61 7 334 62058

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

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

165 works between 2001 and 2024

41 - 60 of 165 works

2021

Journal Article

Caging NLRP3 tames inflammasome activity

Schroder, Kate and Coll, Rebecca C. (2021). Caging NLRP3 tames inflammasome activity. Cell, 184 (26), 6224-6226. doi: 10.1016/j.cell.2021.11.035

Caging NLRP3 tames inflammasome activity

2021

Journal Article

Endothelial cells are not productively infected by SARS‐CoV‐2

Schimmel, Lilian, Chew, Keng Yih, Stocks, Claudia J., Yordanov, Teodor E., Essebier, Patricia, Kulasinghe, Arutha, Monkman, James, Santos Miggiolaro, Anna Flavia Ribeiro, Cooper, Caroline, Noronha, Lucia, Schroder, Kate, Lagendijk, Anne Karine, Labzin, Larisa I., Short, Kirsty R. and Gordon, Emma J. (2021). Endothelial cells are not productively infected by SARS‐CoV‐2. Clinical and Translational Immunology, 10 (10) e1350, e1350. doi: 10.1002/cti2.1350

Endothelial cells are not productively infected by SARS‐CoV‐2

2021

Journal Article

Streptolysins are the primary inflammasome activators in macrophages during Streptococcus pyogenes infection

Richter, Johanna, Monteleone, Mercedes M, Cork, Amanda J., Barnett, Timothy C., Nizet, Victor, Brouwer, Stephan, Schroder, Kate and Walker, Mark J. (2021). Streptolysins are the primary inflammasome activators in macrophages during Streptococcus pyogenes infection. Immunology and Cell Biology, 99 (10), 1-13. doi: 10.1111/imcb.12499

Streptolysins are the primary inflammasome activators in macrophages during Streptococcus pyogenes infection

2021

Journal Article

Inflammasome activation and IL ‐1β signalling in Group A Streptococcus disease

Richter, Johanna, Brouwer, Stephan, Schroder, Kate and Walker, Mark J. (2021). Inflammasome activation and IL ‐1β signalling in Group A Streptococcus disease. Cellular Microbiology, 23 (9) e13373, 1-9. doi: 10.1111/cmi.13373

Inflammasome activation and IL ‐1β signalling in Group A Streptococcus disease

2021

Journal Article

SCIMP is a spatiotemporal transmembrane scaffold for Erk1/2 to direct pro-inflammatory signaling in TLR-activated macrophages

Lucas, Richard M., Liu, Liping, Curson, James E. B., Koh, Yvette W. H., Tuladhar, Neeraj, Condon, Nicholas D., Das Gupta, Kaustav, Burgener, Sabrina S., Schroder, Kate, Ingley, Evan, Sweet, Matthew J., Stow, Jennifer L. and Luo, Lin (2021). SCIMP is a spatiotemporal transmembrane scaffold for Erk1/2 to direct pro-inflammatory signaling in TLR-activated macrophages. Cell Reports, 36 (10) 109662, 1-20. doi: 10.1016/j.celrep.2021.109662

SCIMP is a spatiotemporal transmembrane scaffold for Erk1/2 to direct pro-inflammatory signaling in TLR-activated macrophages

2021

Journal Article

Vincristine-induced peripheral neuropathy is driven by canonical NLRP3 activation and IL-1β release

Starobova, Hana, Monteleone, Mercedes, Adolphe, Christelle, Batoon, Lena, Sandrock, Cheyenne J., Tay, Bryan, Deuis, Jennifer R., Smith, Alexandra V., Mueller, Alexander, Nadar, Evelyn Israel, Lawrence, Grace Pamo, Mayor, Amanda, Tolson, Elissa, Levesque, Jean-Pierre, Pettit, Allison R., Wainwright, Brandon J., Schroder, Kate and Vetter, Irina (2021). Vincristine-induced peripheral neuropathy is driven by canonical NLRP3 activation and IL-1β release. Journal of Experimental Medicine, 218 (5) e20201452. doi: 10.1084/jem.20201452

Vincristine-induced peripheral neuropathy is driven by canonical NLRP3 activation and IL-1β release

2021

Journal Article

The NLRP3 inflammasome triggers sterile neuroinflammation and Alzheimer’s disease

Milner, Mark T, Maddugoda, Madhavi, Götz, Jürgen, Burgener, Sabrina S and Schroder, Kate (2021). The NLRP3 inflammasome triggers sterile neuroinflammation and Alzheimer’s disease. Current Opinion in Immunology, 68, 116-124. doi: 10.1016/j.coi.2020.10.011

The NLRP3 inflammasome triggers sterile neuroinflammation and Alzheimer’s disease

2021

Journal Article

Placental inflammasome signaling: protection for mother and baby

Burgener, Sabrina Sofia and Schroder, Kate (2021). Placental inflammasome signaling: protection for mother and baby. The Journal of Experimental Medicine, 218 (1) e20201738. doi: 10.1084/jem.20201738

Placental inflammasome signaling: protection for mother and baby

2021

Journal Article

The complex interplay between endoplasmic reticulum stress and the NLRP3 inflammasome: a potential therapeutic target for inflammatory disorders

Chong, Wai Chin, Shastri, Madhur D., Peterson, Gregory M., Patel, Rahul P., Pathinayake, Prabuddha S., Dua, Kamal, Hansbro, Nicole G., Hsu, Alan C., Wark, Peter A., Shukla, Shakti Dhar, Johansen, Matt D., Schroder, Kate and Hansbro, Philip M. (2021). The complex interplay between endoplasmic reticulum stress and the NLRP3 inflammasome: a potential therapeutic target for inflammatory disorders. Clinical and Translational Immunology, 10 (2) e1247. doi: 10.1002/cti2.1247

The complex interplay between endoplasmic reticulum stress and the NLRP3 inflammasome: a potential therapeutic target for inflammatory disorders

2020

Journal Article

Lipopolysaccharide promotes Drp1‐dependent mitochondrial fission and associated inflammatory responses in macrophages

Kapetanovic, Ronan, Afroz, Syeda Farhana, Ramnath, Divya, Lawrence, Grace M.E.P., Okada, Takashi, Curson, James E.B., Bruin, Jost, Fairlie, David P., Schroder, Kate, St John, Justin C., Blumenthal, Antje and Sweet, Matthew J. (2020). Lipopolysaccharide promotes Drp1‐dependent mitochondrial fission and associated inflammatory responses in macrophages. Immunology and Cell Biology, 98 (7) imcb.12363, 528-539. doi: 10.1111/imcb.12363

Lipopolysaccharide promotes Drp1‐dependent mitochondrial fission and associated inflammatory responses in macrophages

2020

Journal Article

Design, synthesis and evaluation of an NLRP3 inhibitor diazirine photoaffinity probe

Hill, James R., Coll, Rebecca C., Schroder, Kate and Robertson, Avril A.B. (2020). Design, synthesis and evaluation of an NLRP3 inhibitor diazirine photoaffinity probe. Tetrahedron Letters, 61 (19) 151849, 151849. doi: 10.1016/j.tetlet.2020.151849

Design, synthesis and evaluation of an NLRP3 inhibitor diazirine photoaffinity probe

2020

Journal Article

The rOX‐stars of inflammation: links between the inflammasome and mitochondrial meltdown

Holley, Caroline L. and Schroder, Kate (2020). The rOX‐stars of inflammation: links between the inflammasome and mitochondrial meltdown. Clinical & Translational Immunology, 9 (2) e01109, e01109. doi: 10.1002/cti2.1109

The rOX‐stars of inflammation: links between the inflammasome and mitochondrial meltdown

2020

Journal Article

The microglial NLRP3 inflammasome is activated by amyotrophic lateral sclerosis proteins

Deora, Vandana, Lee, John D., Albornoz, Eduardo A., McAlary, Luke, Jagaraj, Cyril J., Robertson, Avril A. B., Atkin, Julie D, Cooper, Matthew A., Schroder, Kate, Yerbury, Justin J., Gordon, Richard and Woodruff, Trent M. (2020). The microglial NLRP3 inflammasome is activated by amyotrophic lateral sclerosis proteins. Glia, 68 (2) glia.23728, 407-421. doi: 10.1002/glia.23728

The microglial NLRP3 inflammasome is activated by amyotrophic lateral sclerosis proteins

2020

Journal Article

Neutrophil-derived S100A8/A9 amplify granulopoiesis following myocardial infarction

Sreejit, Gopalkrishna, Abdel-Latif, Ahmed, Athmanathan, Baskaran, Annabathula, Rahul, Dhyani, Ashish, Noothi, Sunil K, Quaife-Ryan, Gregory A., Al-Sharea, Annas, Pernes, Gerard, Dragoljevic, Dragana, Lal, Hind, Schroder, Kate, Hanaoka, Beatriz Y., Raman, Chander, Grant, Maria B., Hudson, James E., Smyth, Susan, Porrello, Enzo R., Murphy, Andrew J. and Nagareddy, Prabhakara R. (2020). Neutrophil-derived S100A8/A9 amplify granulopoiesis following myocardial infarction. Circulation, 141 (13), 1080-1094. doi: 10.1161/CIRCULATIONAHA.119.043833

Neutrophil-derived S100A8/A9 amplify granulopoiesis following myocardial infarction

2020

Journal Article

Neutrophil extracellular traps in host defense

Burgener, Sabrina Sofia and Schroder, Kate (2020). Neutrophil extracellular traps in host defense. Cold Spring Harbor Perspectives in Biology, 12 (7) a037028, a037028-15. doi: 10.1101/cshperspect.a037028

Neutrophil extracellular traps in host defense

2019

Conference Publication

New insights into inflammasome signalling and function during inflammation

Schroder, Kate, Boucher, Dave and Coll, Rebecca (2019). New insights into inflammasome signalling and function during inflammation. 48th Annual Scientific Meeting International Society for Experimental Hematology, Brisbane, QLD Australia, 22-25 August 2019. Philadelphia, PA United States: Elsevier . doi: 10.1016/j.exphem.2019.06.258

New insights into inflammasome signalling and function during inflammation

2019

Journal Article

Inhibitors of class I histone deacetylases attenuate thioacetamide-induced liver fibrosis in mice by suppressing hepatic Type 2 inflammation

Loh, Zhixuan, Fitzsimmons, Rebecca L., Reid, Robert C., Ramnath, Divya, Clouston, Andrew, Gupta, Praveer K., Irvine, Katharine M., Powell, Elizabeth E., Schroder, Kate, Stow, Jennifer L., Sweet, Matthew J., Fairlie, David P. and Iyer, Abishek (2019). Inhibitors of class I histone deacetylases attenuate thioacetamide-induced liver fibrosis in mice by suppressing hepatic Type 2 inflammation. British Journal of Pharmacology, 176 (19) bph.14768, 3775-3790. doi: 10.1111/bph.14768

Inhibitors of class I histone deacetylases attenuate thioacetamide-induced liver fibrosis in mice by suppressing hepatic Type 2 inflammation

2019

Journal Article

Lack of protein prenylation promotes NLRP3 inflammasome assembly in human monocytes

Skinner, Oliver P., Jurczyluk, Julie, Baker, Paul J., Masters, Seth L., Rios Wilks, Alicia G., Clearwater, Misaki S., Robertson, Avril A. B., Schroder, Kate, Mehr, Sam, Munoz, Marcia A. and Rogers, Michael J. (2019). Lack of protein prenylation promotes NLRP3 inflammasome assembly in human monocytes. Journal of Allergy and Clinical Immunology, 143 (6), 2315-2317.e3. doi: 10.1016/j.jaci.2019.02.013

Lack of protein prenylation promotes NLRP3 inflammasome assembly in human monocytes

2019

Journal Article

Variation in hemolysin A expression between uropathogenic Escherichia coli isolates determines NLRP3-dependent vs. -independent macrophage cell death and host colonization

Murthy, Ambika M. V., Sullivan, Matthew J., Nhu, Nguyen Thi Khanh, Lo, Alvin W., Phan, Minh-Duy, Peters, Kate M., Boucher, Dave, Schroder, Kate, Beatson, Scott A., Ulett, Glen C., Schembri, Mark A. and Sweet, Matthew J. (2019). Variation in hemolysin A expression between uropathogenic Escherichia coli isolates determines NLRP3-dependent vs. -independent macrophage cell death and host colonization. FASEB Journal : official publication of the Federation of American Societies for Experimental Biology, 33 (6), fj201802100R-7450. doi: 10.1096/fj.201802100R

Variation in hemolysin A expression between uropathogenic Escherichia coli isolates determines NLRP3-dependent vs. -independent macrophage cell death and host colonization

2019

Journal Article

The Salmonella pathogenicity island-2 subverts human NLRP3 and NLRC4 inflammasome responses

Bierschenk, Damien, Monteleone, Mercedes, Moghaddas, Fiona, Baker, Paul J., Masters, Seth L., Boucher, Dave and Schroder, Kate (2019). The Salmonella pathogenicity island-2 subverts human NLRP3 and NLRC4 inflammasome responses. Journal of Leukocyte Biology, 105 (2), 401-410. doi: 10.1002/JLB.MA0318-112RR

The Salmonella pathogenicity island-2 subverts human NLRP3 and NLRC4 inflammasome responses

Funding

Current funding

  • 2024 - 2025
    Hope on the horizon - Harnessing inflammation as a novel diagnostic for chronic liver disease (2024 MSHRSS Co-funded Collaboration Grant led by MSH)
    Metro South Health Research Support Scheme Project Grant
    Open grant
  • 2023 - 2026
    Pyroptotic macrophages posthumously sculpt immune responses
    ARC Discovery Projects
    Open grant
  • 2022 - 2025
    Nuclear alarmins escalate tissue immune responses
    ARC Discovery Projects
    Open grant
  • 2022 - 2026
    Inflammasome inhibitors as new first-in-class anti-inflammatory therapies
    NHMRC Investigator Grants
    Open grant
  • 2022 - 2026
    Mining the host-pathogen interface to deliver a drug pipeline for treating intractable and emerging infections
    NHMRC Synergy Grants
    Open grant

Past funding

  • 2023 - 2024
    Elucidating Cardiolipin and Immune Dysfunction in Barth Syndrome
    The Barth Syndrome Foundation
    Open grant
  • 2021 - 2023
    Accelerating the diagnosis of children with autoinflammatory diseases
    Specific Donations Research Grant
    Open grant
  • 2020 - 2022
    A novel mechanism of host defence via macrophage extracellular traps
    ARC Discovery Projects
    Open grant
  • 2019 - 2021
    Developing treatments for vincristine-induced neuropathy
    The Kid's Cancer Project
    Open grant
  • 2019 - 2023
    Pathogenic functions for the NLRP3 inflammasome in Alzheimer's Disease
    The Yulgilbar Foundation
    Open grant
  • 2019 - 2022
    Molecular determinants of inflammatory caspase activity upon inflammasomes
    ARC Discovery Projects
    Open grant
  • 2019
    Advanced Brightfield and Fluorescent High Speed and Throughput Slide Scanner for biological, medical, materials science, and agricultural applications
    UQ Major Equipment and Infrastructure
    Open grant
  • 2019
    In vivo imaging system for tracking inflammation, infection, cancer, pain and bioactive molecules
    UQ Major Equipment and Infrastructure
    Open grant
  • 2019 - 2021
    PyroNETosis: a new mechanism of host defence
    NHMRC Project Grant
    Open grant
  • 2018
    Epifluorescent and live-cell imaging microscopes for the investigation of host-pathogen interactions and for molecular and cellular biology
    UQ Major Equipment and Infrastructure
    Open grant
  • 2018 - 2021
    Extinguishing the fire: inflammasome inhibition
    NHMRC Career Development Fellowship
    Open grant
  • 2017 - 2024
    ACRF Cancer Ultrastructure and Function Facility
    Australian Cancer Research Foundation
    Open grant
  • 2017 - 2019
    A novel mechanism for IL-1B secretion
    NHMRC Project Grant
    Open grant
  • 2017 - 2019
    Inflammatory pathways to liver fibrosis in non-alcoholic and alcoholic steatohepatitis: reversal by NLRP3 inhibitors (NHMRC Project Grant administered by ANU)
    Australian National University
    Open grant
  • 2016 - 2018
    Pharmacological Targeting of Proinflammatory Kinase Signalling in Parkinson's disease
    The Michael J Fox Foundation for Parkinsons Research
    Open grant
  • 2016 - 2020
    Blocking inflammasome-induced neuroinflammation in PD with a potent, orally available small molecule
    The Michael J Fox Foundation Therapeutic Pipeline Program
    Open grant
  • 2016 - 2019
    A molecular timer for inflammation and cell death
    ARC Discovery Projects
    Open grant
  • 2016 - 2018
    Autophagic suppression of ASC inflammasomes
    NHMRC Project Grant
    Open grant
  • 2015 - 2017
    Pharmacological targeting of the NLRP3 inflammasome in pre-clinical models of Parkinson's disease using a potent orally active inhibitor
    The Michael J Fox Foundation for Parkinsons Research
    Open grant
  • 2015 - 2017
    Inhibitors of NLRP3 activation for treatment of inflammatory CNS diseases
    NHMRC Project Grant
    Open grant
  • 2015
    Murine behavioural phenotyping facility
    UQ Major Equipment and Infrastructure
    Open grant
  • 2015 - 2016
    Therapeutic targeting of the NLRP3 inflammasome using a potent and orally active inhibitor in experimental MND
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2014 - 2018
    Inflammasomes: molecular drivers of anti-microbial defence
    ARC Future Fellowships
    Open grant
  • 2014 - 2016
    Microbial evasion of a novel inflammasome by Salmonella
    NHMRC Project Grant
    Open grant
  • 2014
    Pinpointing the initiation of immune responses
    UQ Foundation Research Excellence Awards - DVC(R) Funding
    Open grant
  • 2013 - 2016
    Caspase 8 apoptotic signalling induced by the inflammasome
    NHMRC Project Grant
    Open grant
  • 2013 - 2015
    Smart Futures Fellowship (Mid): Development of strategies to predict type 2 diabetes risk, and prevent diabetes onset in at-risk Queensland children
    Queensland Government Smart Futures Fellowships
    Open grant
  • 2012 - 2014
    Inflammasome function in neutrophils
    NHMRC Project Grant
    Open grant
  • 2011 - 2012
    NHMRC Training Fellowship (CJ Martin): Inflammasome function in gastrointestinal immunity and inflammation
    NHMRC Training (Postdoctoral) Fellowship
    Open grant
  • 2005 - 2008
    Human macrophage transcriptional network
    Riken Genomic Sciences Center
    Open grant

Supervision

Availability

Professor Kate Schroder is:
Available for supervision

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

Available projects

  • 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

Completed supervision

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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