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Associate Professor Fernando Guimaraes
Associate Professor

Fernando Guimaraes

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Overview

Background

I lead a research program with extensive expertise in immunology, particularly in natural killer (NK) cells, focused on developing innovative approaches for treating hard-to-cure diseases like metastatic cancers. Our mission is to improve patient outcomes and extend lives. My research group is based at the Translational Research Institute (TRI).

My dedication to my field has been recognized through numerous peer-reviwed grants as sole-CI or CIA/Principal Investigator, including a NHMRC ECF Peter Doherty Fellowship, an NHMRC Project Grant, an US DoD, a MRFF EMCR among others. Since 2009, I've amassed an impressive portfolio of 96 publications in renowned journals like Blood, Cell Death Dis, JEM, PNAS, Nat Comms, and Nat Immunol with an H-index = 40. My body of work and contributions have been acknowledged with awards such as the 2019 Researcher of the Year by CCA, 2020 QLD Young Tall Poppy Science, 2020 UQ Frazer Institute's Rising Star, 2022 Frazer Institute's Mentor of the Year, 2023 Translational Research Institute - Connecting with the Clinic among others. Recognized as an international leader in my field, I've been instrumental in identifying novel regulators of our immune functions, and developing NK cell-based immunotherapies.

At present, I am a Group Leader / Principal Research Fellow & Associate Professor with the University of Queensland's Frazer Institute. Here, I lead a high-performing research team with a keen focus on developing and innovating immunotherapy approaches for a spectrum of diseases.

Availability

Associate Professor Fernando Guimaraes is:
Available for supervision
Media expert

Qualifications

  • Doctor of Philosophy, Institution to be confirmed

Research interests

  • NK cells

    Overview: Natural Killer (NK) cells are a crucial component of the innate immune system, recognized for their ability to target and destroy cancerous or infected cells without prior sensitization. Their unique capability to distinguish between healthy and abnormal cells makes them pivotal in immunological defenses and cancer immunosurveillance. Current research: My current research focuses on unraveling the complex interactions of NK cells within various disease environments. We are investigating how NK cells respond to different cancer types, particularly in the context of hard-to-cure solid cancers (e.g. pediatric sarcomas). Our recent findings suggest novel pathways through which NK cells can be modulated to enhance their cytotoxicity against tumor cells. We are also exploring the impact of the tumor microenvironment on NK cell function, hypothesizing that certain microenvironmental factors might inhibit their activity and how this can be counteracted. Future directions: Looking forward, our goal is to develop strategies to boost NK cell efficacy in cancer therapy. This includes genetic engineering of NK cells to enhance their tumor-targeting capabilities and the identification of new biomarkers for predicting patient response to NK cell-based therapies. Our ultimate aim is to leverage NK cells' natural abilities to create more effective and less toxic cancer treatments.

  • Systems immunology and checkpoint discovery

    Explanation of systems immunology: Systems immunology integrates computational and experimental approaches to understand the immune system's complexity. By analyzing vast datasets, we can decipher the intricate network of cellular interactions and molecular pathways that govern immune responses in diseases ranging from viral infections to cancer. Immunomodulation and disease environments: Our research in systems immunology focuses on understanding how immunomodulation varies across different disease states. We are particularly interested in how immune checkpoints, which are regulatory pathways crucial to maintaining self-tolerance and preventing autoimmunity, can be exploited or inhibited in disease contexts. For instance, we are exploring how tumor cells evade immune surveillance by manipulating these checkpoints. Impact of Research: This research holds significant promise for unveiling new therapeutic targets and developing personalized medicine approaches. Understanding these complex immune interactions can lead to the discovery of novel treatments that precisely modulate the immune system to combat various diseases effectively.

  • Development of tailored immunotherapies

    Introduction to tailored immunotherapies: Tailored immunotherapies represent a revolutionary approach in medicine, offering treatments that are specifically designed to match an individual's unique immune profile. This personalized approach is particularly crucial in treating hard-to-cure diseases, where standard therapies often fall short. From antibody discovery to development: My team is actively engaged in the discovery and development of novel antibodies. We focus on identifying antibodies that can specifically target and modulate key components of the immune system. The journey from discovery to development involves extensive research to ensure efficacy and safety, with a keen focus on creating therapies that can be personalized for individual patients. Cellular immunotherapies: Our work in cellular immunotherapies involves engineering immune cells, such as T-cells and NK cells, to better recognize and attack cancer cells. We are exploring various techniques, including CAR-NK cell therapy, to enhance these cells' ability to fight cancer more effectively. Real-world applications: The potential real-world applications of our research are vast. For example, our work in antibody development could lead to new treatments for autoimmune diseases or cancer. Similarly, our advancements in cellular therapies could revolutionize the way we treat various forms of cancer, offering hope to patients with previously untreatable conditions.

Works

Search Professor Fernando Guimaraes’s works on UQ eSpace

122 works between 2009 and 2025

121 - 122 of 122 works

2009

Journal Article

Genome size evaluation in tetraodontiform fishes from the neotropical region

Noleto, Rafael Bueno, de Fonseca Souza Guimarães, Fernando, Paludo, Katia Sabrina, Vicari, Marcelo Ricardo, Artoni, Roberto Ferreira and Cestari, Marta Margarete (2009). Genome size evaluation in tetraodontiform fishes from the neotropical region. Marine Biotechnology, 11 (6), 680-685. doi: 10.1007/s10126-009-9215-0

Genome size evaluation in tetraodontiform fishes from the neotropical region

2009

Journal Article

Establishment of experimental conditions for preserving samples of fish blood for analysis with both comet assay and flow cytometry

Ramsdorf, Wanessa A., Guimarães, Fernando de S.F., Ferraro, Marcos V.M., Gabardo, Juarez, Trindade, Edvaldo da Silva and Cestari, Marta Margarete (2009). Establishment of experimental conditions for preserving samples of fish blood for analysis with both comet assay and flow cytometry. Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 673 (1), 78-81. doi: 10.1016/j.mrgentox.2008.11.010

Establishment of experimental conditions for preserving samples of fish blood for analysis with both comet assay and flow cytometry

Funding

Current funding

  • 2024 - 2027
    Treating breast cancer metastasis by targeting immunosuppressive extracellular vesicles
    National Breast Cancer Foundation
    Open grant
  • 2024 - 2025
    NK Cell Scale Up: Training Natural Killer cells for Immunotherapy for children, adolescent and adults with Sarcoma
    The Kid's Cancer Project
    Open grant
  • 2024 - 2034
    Training Natural Killer Cells for Immunotherapy for Children, Adolescent, and Adults with Sarcoma
    Cooper Rice-Brading Foundation Ltd/Tie Dye Project
    Open grant
  • 2023 - 2025
    Utilising alternative cytokine receptor signalling for enhanced cell-based cancer immunotherapy
    Australia's Economic Accelerator Seed Grants
    Open grant
  • 2023 - 2026
    Multi-omics data integration to elucidate novel mechanisms of lung pathology during bacterial or viral infection
    University of Technology Sydney
    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

Past funding

  • 2023 - 2024
    Assessment of CellPryme supplementation in the enhancement of natural killer cell functions
    Prescient Therapeutics Limited
    Open grant
  • 2023
    Assessment of immunotherapeutic potential of novel microbial-derived products
    Innovation Connections
    Open grant
  • 2023 - 2024
    Reversing tumour necrosis factor-mediated immunosuppression to boost immunity against experimental CD19+ blood cancers
    Metro South Hospital and Health Service
    Open grant
  • 2021 - 2023
    Targeting and eliminating paediatric cancers with chimeric antigen receptor engineered natural killer cells, a new hope for cancer immunotherapy
    Children's Hospital Foundation Immunotherapy Research Grants
    Open grant
  • 2021 - 2022
    Development of a natural killer cell-based immunotherapy for Rhabdomyosarcoma
    ANZ Sarcoma Research Grant
    Open grant
  • 2021 - 2024
    Enhancement of Natural Killer Cell Function for Therapeutic Targeting and Elimination of Metastatic Breast Cancer
    United States Congressionally Directed Medical Research Programs - Breast Cancer Research Program
    Open grant
  • 2020 - 2021
    Development of new anti-breast cancer antibodies for natural killer (NK)-based immunotherapy
    Therapeutic Innovation Australia Limited
    Open grant
  • 2019 - 2021
    Targeting alternative SMAD-related suppressive signalling pathway enhance NK cell response
    Cancer Australia
    Open grant
  • 2019 - 2021
    Interactions between IL-15 and TGF-beta signalling pathways reveal novel therapeutic strategies to boost anticancer immunity
    NHMRC Project Grant
    Open grant

Supervision

Availability

Associate Professor Fernando Guimaraes is:
Available for supervision

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Available projects

  • Which tumour immunosuppressive pathways prevent natural killer cell activation?

    Background: Despite advances in treatment and earlier detection, cancer is still a main cause of cancer death worldwide. Natural killer (NK) cells are circulating innate lymphocytes that naturally protect against tumor spread (metastasis), and recently showed by our group as dysfunctional in the tumour microenvironment (TME) established by cancers at distant organs for future metastatic spread. Yet, despite knowing that NK cells do control cancer metastasis, our knowledge of how cancer cells evade NK cell control is still very poor. This project aims to examine several immune suppressive pathways that cancers likely manipulate to avoid NK cells and spread. These include factors the transforming growth factor (TGF)-β superfamily that are elevated in the tumor environment. These molecules have great potential to suppress the normally high killing and anti-metastatic activity mediated by NK cells, but to date we still need to elucidate how relatively important each pathway might be.

    Proposed research program: The intrinsic NK cell function under suppressive factors stimulation will be assessed with NK cells purified from mouse spleen (wild type) by cell sorter, and in vitro challenge with activating cytokines and suppressive factors. Aim-1: Which suppressive factor is a major inhibitor of NK cell killing activity? This aim will be screened by killing activity of NK cells versus target tumour cells in co-culture systems. Aim-2: Which suppressive factor is a major inhibitor of NK cell cytokine secretion? This aim will assess NK cell cytokine production by intracellular cytokine (e.g. IFN-gamma) staining (flow cytometry) and secreted IFN-gamma, among others, from culture supernatants (ELISA); Aim-3: What is the cellular signalling status under suppressive conditions? The identification of altered cellular signalling will be screened by intracellular staining of phosphorylated signalling molecules (phosphor(p)-AKT, p-ERK1/2, p-p38, p-phospholipase C-gamma2, p-phosphotyrosine, p-SMAD2,3, p-STAT4, p-STAT5 and p-ZAP70 (PhosphoFlow).

    These experimental tools will determine which is the most important suppressive pathway in inhibiting NK cell functions. Information we obtain from this work will allow us to design rationale approaches to increase NK cell function in personalised immunotherapy approaches.

Supervision history

Current supervision

Completed supervision

Media

Enquiries

Contact Associate Professor Fernando Guimaraes directly for media enquiries about:

  • Cancer research
  • Immunotherapy
  • Natural Killer cells

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