Skip to menu Skip to content Skip to footer
Dr Eduardo Albornoz Balmaceda
Dr

Eduardo Albornoz Balmaceda

Email: 
Phone: 
+61 7 344 38669

Overview

Background

Dr Eduardo Albornoz is a neuroimmunologist whose research focuses on how innate immune mechanisms contribute to neurodegenerative disease. His work investigates how inflammasome and complement pathways are activated by environmental, infectious, and disease-related triggers in conditions such as Parkinson’s disease and motor neuron disease.

Dr Albornoz has expertise in neuroscience, immunology, pharmacology, translational drug development, and preclinical disease modelling. His research integrates human microglia, brain organoids, viral infection models, and animal models to understand how neuroinflammation contributes to neuronal injury and disease progression.

He completed his PhD at The University of Queensland, where he contributed to the development of next-generation NLRP3 inflammasome inhibitors and helped validate NLRP3 as a therapeutic target in Parkinson’s disease. This work supported translational drug development programs that progressed towards clinical testing.

His current research program focuses on environmental and infectious drivers of neurodegeneration, including pesticides, microplastics, PFAS, SARS-CoV-2, and other neurotropic viruses. A major focus of his work is understanding how multiple environmental, infectious, and proteopathic “hits” interact to amplify chronic neuroinflammation and accelerate neurodegenerative disease progression. His research aims to identify therapeutic strategies targeting innate immune pathways to slow or prevent neurodegeneration.

Availability

Dr Eduardo Albornoz Balmaceda is:
Available for supervision
Media expert

Qualifications

  • Masters (Research) of Biochemistry, Universidad Andrés Bello
  • Doctor of Philosophy of Neurosciences, The University of Queensland

Research interests

  • Neuroinflammation and Neurodegeneration

    Research focused on how innate immune pathways drive neurodegenerative diseases including Parkinson’s disease and motor neuron disease. Investigating how chronic neuroinflammation contributes to neuronal injury, disease progression, and therapeutic response

  • Inflammasome and Complement Biology

    Investigating the role of inflammasome and complement pathways in chronic neuroinflammation and neurodegeneration. Research aims to identify how these innate immune systems interact to amplify neuronal injury and contribute to disease progression.

  • Environmental Drivers of Neurodegeneration

    Research examining how environmental exposures, including pesticides, microplastics, and PFAS, contribute to neuroinflammation and neurodegenerative disease. Focused on understanding how multiple environmental and disease-related “hits” interact to drive chronic inflammatory responses in the brain.

  • Viral Neuroimmunology

    Investigating how viral infections, including SARS-CoV-2 and neurotropic flaviviruses, activate inflammatory pathways associated with neurodegeneration. Research includes mechanisms linking viral infection, cellular senescence, and chronic neuroinflammation.

  • Human Microglia and Brain Organoids

    Development and application of advanced human-relevant experimental models, including patient-derived microglia and brain organoids, to study neuroinflammation, neurodegeneration, and therapeutic responses in translational neuroscience research.

  • Translational Neuroimmunology and Drug Development

    Research focused on translating neuroimmunology discoveries into therapeutic strategies targeting innate immune pathways. Includes development and preclinical evaluation of immunomodulatory therapies for neurodegenerative disease.

Research impacts

Dr Albornoz’s research investigates how environmental, infectious, and disease-related factors trigger harmful inflammatory responses in the brain that contribute to neurodegenerative disease progression.

His work helped validate the NLRP3 inflammasome as a therapeutic target in Parkinson’s disease and contributed to the development of next-generation inflammasome inhibitors through collaboration with Inflazome, later acquired by Roche. His research has also contributed to understanding how complement and inflammasome pathways interact to amplify chronic neuroinflammation and neuronal injury in neurodegenerative disease. Together, this work formed part of translational drug development programs progressing towards clinical testing and contributed to one of UQ’s most successful biomedical commercialisation outcomes.

His studies on SARS-CoV-2, neuroinflammation, and cellular senescence provided some of the first mechanistic evidence linking viral infection to activation of inflammatory pathways associated with neurodegeneration. This work received international attention through extensive media coverage, strong citation impact, and recognition as a highly cited and “hot” publication.

A major focus of Dr Albornoz’s research is understanding how multiple environmental, infectious, and disease-related “hits” interact to amplify chronic inflammation, neuronal injury, cellular dysfunction, and self-sustaining cycles of immune activation in the brain. This work aims to improve understanding of modifiable disease risk factors and identify opportunities for earlier therapeutic intervention, disease prevention, and development of new immunomodulatory therapies.

His research also contributes to development of advanced human-relevant experimental models, including patient-derived microglia and human brain organoids, supporting more predictive preclinical testing and translational neuroscience research.

Through collaborations with academic, biotechnology, and clinical research partners, his work supports the translation of neuroimmunology discoveries into therapeutic development and improved understanding of neurodegenerative disease mechanisms.

Works

Search Professor Eduardo Albornoz Balmaceda’s works on UQ eSpace

28 works between 2013 and 2026

1 - 20 of 28 works

2026

Journal Article

PET-MRI biomarkers reveal efficacy of a novel NLRP3 inhibitor in Parkinson’s disease models

Albornoz, Eduardo A., Mardon, Karine, Bhalla, Rajiv, Kumar, Vinod, Stimson, Damion H. R., Cowin, Gary, Cui, Cedric S., Butler, Mark S., Pelingon, Ruby, Gordon, Richard, Coll, Rebecca C., Schroder, Kate, Halai, Reena, MacLeod, Angus M., Matthews, Kim, Robertson, Avril A. B., Cooper, Matthew A. and Woodruff, Trent M. (2026). PET-MRI biomarkers reveal efficacy of a novel NLRP3 inhibitor in Parkinson’s disease models. Brain, 149 (4) awaf372, 1289-1301. doi: 10.1093/brain/awaf372

PET-MRI biomarkers reveal efficacy of a novel NLRP3 inhibitor in Parkinson’s disease models

2025

Journal Article

Complement C9-mediated RBC hemolysis drives microvascular obstruction via endothelial necroptosis and hemolyzed RBC aggregation in COVID-19

Lun (Mike) Wu, Chia, Ju, Lining Arnold, Italiano, Ethan, Jarvis-Child, Rocko, Alwis, Imala, Smythe, Rhyll, Albornoz, Eduardo A., Noonan, Jonathan, Portelli, Marie, Baptista, Marrisa, Maclean, Jessica, Norri, Pashtana, Yang, Jinglu, Lee, John, McFadyen, James D., Sharland, Alexandra, Woodruff, Trent M., Samson, Andre, Rapkiewicz, Amy, Barrett, Tessa, Pham, Alan, Schoenwaelder, Simone, Yuan, Yuping and Jackson, Shaun P. (2025). Complement C9-mediated RBC hemolysis drives microvascular obstruction via endothelial necroptosis and hemolyzed RBC aggregation in COVID-19. Immunobiology, 230 (4) 153045, 53-53. doi: 10.1016/j.imbio.2025.153045

Complement C9-mediated RBC hemolysis drives microvascular obstruction via endothelial necroptosis and hemolyzed RBC aggregation in COVID-19

2025

Conference Publication

Motor neuron disease C9orf72 dipeptides mediate neurotoxicity in human brain organoids through activation of C5aR1

Cao, Yuzhihan, Pietrogrande, Giovanni, Pars, Selin, Clark, Richard, Wolvetang, Ernst, Woodruff, Trent and Albornoz, Eduardo (2025). Motor neuron disease C9orf72 dipeptides mediate neurotoxicity in human brain organoids through activation of C5aR1. 30th International Complement Workshop 2025, Brisbane, QLD, Australia, 14-19 September 2025. Munich, Germany: Elsevier. doi: 10.1016/j.imbio.2025.153008

Motor neuron disease C9orf72 dipeptides mediate neurotoxicity in human brain organoids through activation of C5aR1

2025

Conference Publication

Live-cell single-molecule imaging of a new fluorescent C5a receptor antagonist reveals the heterogeneous spatiotemporal dynamics of C5aR1 at the plasma membrane

Sun, Jinda, Parker, Sandra, Lee, Jonathan, Gorman, Declan, Li, Xaria, Albornoz Balmaceda, Eduardo, Bellingham, Mark, Clark, Richard, Woodruff, Trent and Padmanabhan, Pranesh (2025). Live-cell single-molecule imaging of a new fluorescent C5a receptor antagonist reveals the heterogeneous spatiotemporal dynamics of C5aR1 at the plasma membrane. 30th International Complement Workshop 2025, Brisbane, QLD, Australia, 14-19 September 2025. Munich, Germany: Elsevier. doi: 10.1016/j.imbio.2025.152969

Live-cell single-molecule imaging of a new fluorescent C5a receptor antagonist reveals the heterogeneous spatiotemporal dynamics of C5aR1 at the plasma membrane

2025

Conference Publication

Microglial Complement C5aR1 signalling drives inflammasome mediated neuropathology in Parkinson’s disease

Albornoz, Eduardo, Gordon, Richard, Javed, Ibrahim, Bodea, Gabriela, Kumar, Vinod, Cui, Cedric, Aguado, Julio, Mardon, Karine, Bhalla, Rajiv, Cowin, Gary and Woodruff, Trent (2025). Microglial Complement C5aR1 signalling drives inflammasome mediated neuropathology in Parkinson’s disease. 30th International Complement Workshop 2025, Brisbane, QLD Australia, 14-19 September 2025. Muenchen, Germany: Elsevier. doi: 10.1016/j.imbio.2025.152955

Microglial Complement C5aR1 signalling drives inflammasome mediated neuropathology in Parkinson’s disease

2025

Journal Article

Ischaemic endothelial necroptosis induces haemolysis and COVID-19 angiopathy

Wu, Mike C. L., Italiano, Ethan, Jarvis-Child, Rocko, Alwis, Imala, Smythe, Rhyll, Albornoz, Eduardo A., Noonan, Jonathan, Portelli, Marie, Baptista, Marissa, Maclean, Jessica, Noori, Pashtana, Yang, Jinglu, Lee, John D., McFadyen, James D., Sharland, Alexandra F., Woodruff, Trent M., Samson, Andre L., Rapkiewicz, Amy, Barrett, Tessa J., Pham, Alan, Schoenwaelder, Simone M., Yuan, Yuping and Jackson, Shaun P. (2025). Ischaemic endothelial necroptosis induces haemolysis and COVID-19 angiopathy. Nature, 643 (8070), 182-191. doi: 10.1038/s41586-025-09076-x

Ischaemic endothelial necroptosis induces haemolysis and COVID-19 angiopathy

Featured

2023

Journal Article

Senolytic therapy alleviates physiological human brain aging and COVID-19 neuropathology

Aguado, Julio, Amarilla, Alberto A., Taherian Fard, Atefeh, Albornoz, Eduardo A., Tyshkovskiy, Alexander, Schwabenland, Marius, Chaggar, Harman K., Modhiran, Naphak, Gómez-Inclán, Cecilia, Javed, Ibrahim, Baradar, Alireza A., Liang, Benjamin, Peng, Lianli, Dharmaratne, Malindrie, Pietrogrande, Giovanni, Padmanabhan, Pranesh, Freney, Morgan E., Parry, Rhys, Sng, Julian D. J., Isaacs, Ariel, Khromykh, Alexander A., Valenzuela Nieto, Guillermo, Rojas-Fernandez, Alejandro, Davis, Thomas P., Prinz, Marco, Bengsch, Bertram, Gladyshev, Vadim N., Woodruff, Trent M., Mar, Jessica C. ... Wolvetang, Ernst J. (2023). Senolytic therapy alleviates physiological human brain aging and COVID-19 neuropathology. Nature Aging, 3 (12), 1561-1575. doi: 10.1038/s43587-023-00519-6

Senolytic therapy alleviates physiological human brain aging and COVID-19 neuropathology

2023

Journal Article

200 Complement drives Parkinson’s disease neuropathology through activation of microglial C5a receptors

Albornoz, Eduardo and Woodruff, Trent (2023). 200 Complement drives Parkinson’s disease neuropathology through activation of microglial C5a receptors. Immunobiology, 228 (5) 152650, 1-1. doi: 10.1016/j.imbio.2023.152650

200 Complement drives Parkinson’s disease neuropathology through activation of microglial C5a receptors

Featured

2023

Journal Article

Response to comment on “Inflammasome inhibition prevents α-synuclein pathology and dopaminergic neurodegeneration in mice”

Albornoz, Eduardo A., Gordon, Richard, Kumar, Vinod, Robertson, Avril A. B., Schroder, Kate and Woodruff, Trent M. (2023). Response to comment on “Inflammasome inhibition prevents α-synuclein pathology and dopaminergic neurodegeneration in mice”. Science Translational Medicine, 15 (696) adh0604, 1-4. doi: 10.1126/scitranslmed.adh0604

Response to comment on “Inflammasome inhibition prevents α-synuclein pathology and dopaminergic neurodegeneration in mice”

2023

Journal Article

SARS-CoV-2 drives NLRP3 inflammasome activation in human microglia through spike protein

Albornoz, Eduardo A., Amarilla, Alberto A., Modhiran, Naphak, Parker, Sandra, Li, Xaria X., Wijesundara, Danushka K., Aguado, Julio, Zamora, Adriana Pliego, McMillan, Christopher L. D., Liang, Benjamin, Peng, Nias Y. G., Sng, Julian D. J., Saima, Fatema Tuj, Fung, Jenny N., Lee, John D., Paramitha, Devina, Parry, Rhys, Avumegah, Michael S., Isaacs, Ariel, Lo, Martin W., Miranda-Chacon, Zaray, Bradshaw, Daniella, Salinas-Rebolledo, Constanza, Rajapakse, Niwanthi W., Wolvetang, Ernst J., Munro, Trent P., Rojas-Fernandez, Alejandro, Young, Paul R., Stacey, Katryn J. ... Woodruff, Trent M. (2023). SARS-CoV-2 drives NLRP3 inflammasome activation in human microglia through spike protein. Molecular Psychiatry, 28 (7), 2878-2893. doi: 10.1038/s41380-022-01831-0

SARS-CoV-2 drives NLRP3 inflammasome activation in human microglia through spike protein

2022

Journal Article

SARS-CoV-2 triggers complement activation through interactions with heparan sulfate

Lo, Martin W., Amarilla, Alberto A., Lee, John D., Albornoz, Eduardo A., Modhiran, Naphak, Clark, Richard J., Ferro, Vito, Chhabra, Mohit, Khromykh, Alexander A., Watterson, Daniel and Woodruff, Trent M. (2022). SARS-CoV-2 triggers complement activation through interactions with heparan sulfate. Clinical and Translational Immunology, 11 (8) e1413, e1413. doi: 10.1002/cti2.1413

SARS-CoV-2 triggers complement activation through interactions with heparan sulfate

2022

Journal Article

Nucleocapsid specific diagnostics for the detection of divergent SARS-CoV-2 variants

Isaacs, Ariel, Amarilla, Alberto A., Aguado, Julio, Modhiran, Naphak, Albornoz, Eduardo A., Baradar, Alireza A., McMillan, Christopher L. D., Choo, Jovin J. Y., Idris, Adi, Supramaniam, Aroon, McMillan, Nigel A. J., Muller, David A., Young, Paul R., Woodruff, Trent M., Wolvetang, Ernst J., Chappell, Keith J. and Watterson, Daniel (2022). Nucleocapsid specific diagnostics for the detection of divergent SARS-CoV-2 variants. Frontiers in Immunology, 13 926262, 926262. doi: 10.3389/fimmu.2022.926262

Nucleocapsid specific diagnostics for the detection of divergent SARS-CoV-2 variants

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

2019

Other Outputs

Pharmacological targeting of the inflammasome: towards novel therapeutics for Parkinson’s disease

Albornoz Balmaceda, Eduardo (2019). Pharmacological targeting of the inflammasome: towards novel therapeutics for Parkinson’s disease. PhD Thesis, Faculty of Medicine, The University of Queensland. doi: 10.14264/uql.2019.702

Pharmacological targeting of the inflammasome: towards novel therapeutics for Parkinson’s disease

Featured

2018

Journal Article

Inflammasome inhibition prevents α-synuclein pathology and dopaminergic neurodegeneration in mice

Gordon, Richard, Albornoz, Eduardo A., Christie, Daniel C., Langley, Monica R., Kumar, Vinod, Mantovani, Susanna, Robertson, Avril A. B., Butler, Mark S., Rowe, Dominic B., O'Neill, Luke A., Kanthasamy, Anumantha G., Schroder, Kate, Cooper, Matthew A. and Woodruff, Trent M. (2018). Inflammasome inhibition prevents α-synuclein pathology and dopaminergic neurodegeneration in mice. Science Translational Medicine, 10 (465) aah4066, eaah4066. doi: 10.1126/scitranslmed.aah4066

Inflammasome inhibition prevents α-synuclein pathology and dopaminergic neurodegeneration in mice

2018

Journal Article

Gestational hypothyroxinemia affects its offspring with a reduced suppressive capacity impairing the outcome of the experimental autoimmune encephalomyelitis

Haensgen, Henny, Albornoz, Eduardo, Opazo, María C., Bugueño, Katherinne, Jara Fernández, Evelyn Liliana, Binzberger, Rebecca, Rivero-Castillo, Tomás, Venegas Salas, Luis F., Simon, Felipe, Cabello-Verrugio, Claudio, Elorza, Alvaro A., Kalergis, Alexis M., Bueno, Susan M. and Riedel, Claudia A. (2018). Gestational hypothyroxinemia affects its offspring with a reduced suppressive capacity impairing the outcome of the experimental autoimmune encephalomyelitis. Frontiers in Immunology, 9 (JUN) 1257. doi: 10.3389/fimmu.2018.01257

Gestational hypothyroxinemia affects its offspring with a reduced suppressive capacity impairing the outcome of the experimental autoimmune encephalomyelitis

2018

Journal Article

Gestational hypothyroxinemia imprints a switch in the capacity of astrocytes and microglial cells of the offspring to react in inflammation

Opazo, María C., González, Pablo A., Flores, Betsi D., Venegas, Luis F., Albornoz, Eduardo A., Cisternas, Pablo, Bohmwald, Karen, Nieto, Pamela A., Bueno, Susan M., Kalergis, Alexis M. and Riedel, Claudia A. (2018). Gestational hypothyroxinemia imprints a switch in the capacity of astrocytes and microglial cells of the offspring to react in inflammation. Molecular Neurobiology, 55 (5), 4373-4387. doi: 10.1007/s12035-017-0627-y

Gestational hypothyroxinemia imprints a switch in the capacity of astrocytes and microglial cells of the offspring to react in inflammation

2018

Journal Article

Chronic helminth infection perturbs the gut-brain axis, promotes neuropathology and alters behaviour

Giacomin, Paul R., Kraeuter, Ann Katrin, Albornoz, Eduardo A., Jin, Shuting, Bengtsson, Mia, Gordon, Richard, Woodruff, Trent M., Urich, Tim, Sarnyai, Zoltán and Soares Magalhães, Ricardo J. (2018). Chronic helminth infection perturbs the gut-brain axis, promotes neuropathology and alters behaviour. The Journal of Infectious Diseases, 218 (9), 1511-1516. doi: 10.1093/infdis/jiy092

Chronic helminth infection perturbs the gut-brain axis, promotes neuropathology and alters behaviour

2018

Conference Publication

C5aR1 is required for a-synuclein mediated NLRP3 inflammasome activation

Gordon, Richard, Albornoz, Eduardo, Kanthasamy, Anumantha and Woodruff, Trent (2018). C5aR1 is required for a-synuclein mediated NLRP3 inflammasome activation. 27th International Complement Workshop (ICW), Santa Fe, NM, United States, Sep 16-20, 2018. Kidlington, Oxford, United Kingdom: Pergamon Press. doi: 10.1016/j.molimm.2018.06.247

C5aR1 is required for a-synuclein mediated NLRP3 inflammasome activation

2018

Book Chapter

Inflammasomes in CNS diseases

Albornoz, Eduardo A., Woodruff, Trent M. and Gordon, Richard (2018). Inflammasomes in CNS diseases. Inflammasomes: clinical and therapeutic implications. (pp. 41-60) edited by Mario D. Cordero and Elisabet Alcocer-Gómez. Cham, Switzerland: Springer International. doi: 10.1007/978-3-319-89390-7_3

Inflammasomes in CNS diseases

Funding

Past funding

  • 2025 - 2026
    A Novel Patient-Derived Microglia-Brain Organoid Model to accelerate drug discovery in MND
    Motor Neurone Disease Research Institute of Australia Inc Innovator Grant
    Open grant
  • 2023 - 2024
    C9orf72 dipeptide-mediated activation of microglia as a therapeutic target for MND
    Motor Neurone Disease Research Institute of Australia Inc Innovator Grant
    Open grant
  • 2020 - 2021
    Inflammatory biomarkers in 6-OHDA mouse model of Parkinson's disease
    UniQuest Pty Ltd
    Open grant

Supervision

Availability

Dr Eduardo Albornoz Balmaceda is:
Available for supervision

Looking for a supervisor? Read our advice on how to choose a supervisor.

Available projects

  • Environmental Drivers of Neuroinflammation in Parkinson’s Disease

    This project investigates how environmental exposures, including pesticides, microplastics, and PFAS, contribute to chronic neuroinflammation and neurodegeneration in Parkinson’s disease. The student will use advanced human-relevant models, including patient-derived microglia and brain organoids, to study how environmental and disease-related factors interact to activate innate immune pathways.

  • Viral Infection and Neurodegeneration

    This project examines how viral infections, including SARS-CoV-2 and neurotropic viruses, trigger inflammatory responses associated with neurodegenerative disease. Research will focus on mechanisms linking viral infection, cellular senescence, and chronic neuroinflammation using translational human and preclinical models.

  • Inflammasome and Complement Pathways in Neurodegenerative Disease

    This project investigates how innate immune pathways, including inflammasome and complement signalling, contribute to neuronal injury and disease progression in Parkinson’s disease and motor neuron disease. The project will involve molecular, cellular, and translational neuroscience approaches to identify potential therapeutic targets.

Supervision history

Current supervision

  • Doctor Philosophy

    Pathomechanisms in Alzheimer's disease

    Associate Advisor

    Other advisors: Dr Pranesh Padmanabhan

  • Doctor Philosophy

    Therapeutic blockade of neuroinflammation for the treatment of Huntington's disease

    Associate Advisor

    Other advisors: Dr John Lee, Professor Trent Woodruff

Media

Enquiries

Contact Dr Eduardo Albornoz Balmaceda directly for media enquiries about:

  • C5aR
  • Complement system
  • Drug discovery
  • Immunology
  • Infectious disease and brain
  • Inflammasomes
  • Long COVID
  • Microglia
  • Neuroimmunology
  • Neuroinflammation
  • Neuroscience
  • NLRP3
  • Parkinson's disease

Need help?

For help with finding experts, story ideas and media enquiries, contact our Media team:

communications@uq.edu.au