Researchers build new antibody to target cancer cells

Publicly released:
Australia; QLD
The University of Queensland.
The University of Queensland.

A cancer-targeting antibody that helps the body’s immune cells spot and destroy hard-to-treat tumours such as triple-negative breast cancer has been developed by researchers

Media release

From: The University of Queensland

A cancer-targeting antibody that helps the body’s immune cells spot and destroy hard-to-treat tumours such as triple-negative breast cancer has been developed by researchers.

The University of Queensland’s Associate Professor Fernando Guimaraes said the antibody recognises a unique part of the ROR1 protein, which is found on many aggressive cancers but rarely on healthy cells.

“The antibody precisely targets cancer cells, helping the immune system kill cancer more effectively while aiming to spare healthy tissue,’’ Dr Guimaraes said.

“This could translate to treatments that are both more effective and gentler.’’

Dr Guimaraes, whose group at the Frazer Institute led the research, said the new antibody activated natural killer (NK) cells – a type of immune cell that destroys tumours.

The researchers found the antibody worked best when combined with treatment that blocked a cancer immuno-suppressing signal – Transforming Growth Factor-beta or TGF-β.

“We engineered ‘super NK cells’ to boost cancer control,’’ Dr Guimaraes said.

“By giving NK cells a genetic upgrade and making them resistant to TGF-β, we created enhanced immune cells that were able to find and destroy ROR1-positive tumours more efficiently in both laboratory and animal models.

“Triple negative breast cancer is an aggressive and difficult-to-treat cancer, with limited effective therapeutic options currently available.

“Our results open the door to new immunotherapy options, including an upgraded version of NK cells that are better at finding and killing cancer.’’

Dr Guimaraes said the results provide a foundation for future research into clinical applications.

“If successful in people, this approach could improve survival and quality of life by shrinking tumours with fewer side effects than some current therapies,’’ he said.

“In practical terms this could lead to clinical trials and, longer term, new treatment choices for patients who currently have few.’’

The research is published in Molecular Therapy.

Journal/
conference:
Molecular Therapy
Research:Paper
Organisation/s: The University of Queensland, Translational Research Institute (TRI)
Funder: This research was carried out at the Translational Research Institute, Woolloongabba, QLD 4102, Australia. The Translational Research Institute is supported by grants from the Australian and Queensland Governments. This research was supported by Australian Government Research Training Program Scholarships to J.K.M.W, L.A., E.C., C.T. and B.D. The Guimaraes Laboratory was funded by a US Department of Defense – Breast Cancer Research Program – Breakthrough Award Level 1 (#BC200025); by a Metro South Health Research Support Scheme – Co-Funded Collaboration Grant (#RSS_2023_085); a grant (#2019485) awarded through the Medical Research Future Fund (MRFF, in a co-funded partnership with the QLD Children’s Hospital Foundation, Microba Life Sciences, Miltenyi Biotec, the Richie’s Rainbow Foundation, the Translational Research Institute, and UQ); a voucher from the Therapeutic Innovation – Pipeline Accelerator (2020-21-Round_01), a grant from the National Breast Cancer Foundation (#2023/IIRS0063), and funding from the Cooper Rice-Brading Foundation, The Tie Dye Project, The Kids Cancer Project, Bricks & Smiles, Tour de Cure, and the PA Research Foundation. Elements of this work were performed by the National Biologics Facility and the BASE mRNA Facility, both of which are supported by Therapeutic Innovation Australia and the National Collaborative Research Infrastructure Strategy. L.G.A is supported by a National Health and Medical Research Council EL2 Fellowship (APP2034399).
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