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
Fields of research
Qualifications
- Masters (Research) of Biochemistry, Universidad Andrés Bello
- Doctor of Philosophy of Neurosciences, The University of Queensland
Research interests
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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
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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.
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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.
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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.
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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.
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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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Funding
Past funding
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
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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.
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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.
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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
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Doctor Philosophy
Pathomechanisms in Alzheimer's disease
Associate Advisor
Other advisors: Dr Pranesh Padmanabhan
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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
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