The secret life of CD4+ T cells: from helpers to melanoma fighters
In the study led by the Peter Doherty Institute for Infection and Immunity (Doherty Institute) and published in Science Immunology, the researchers found that CD4+ T cells, traditionally called ‘helper T cells’ for their role in aiding the activation of other immune cells, are remarkably effective in controlling melanoma. Credit: Credit: Dr Bawden / Doherty […]
In the study led by the Peter Doherty Institute for Infection and Immunity (Doherty Institute) and published in Science Immunology, the researchers found that CD4+ T cells, traditionally called ‘helper T cells’ for their role in aiding the activation of other immune cells, are remarkably effective in controlling melanoma.
Credit: Credit: Dr Bawden / Doherty Institute
In the study led by the Peter Doherty Institute for Infection and Immunity (Doherty Institute) and published in Science Immunology, the researchers found that CD4+ T cells, traditionally called ‘helper T cells’ for their role in aiding the activation of other immune cells, are remarkably effective in controlling melanoma.
University of Melbourne’s Dr Emma Bawden, Postdoctoral Researcher at the Doherty Institute and lead author of the study, said this discovery challenges the conventional understanding of the role of CD4+ T cells in cancer immunity.
“Our in-depth study, using animal models, unravelled the complex biology of CD4+ T cells in melanoma and how they control cancer,” explained Dr Bawden.
“Using microscopic live imaging, we visualised the activities and interactions of CD4+ T cells with other cell types in the tumour microenvironment. Our findings challenge previous assumptions by showing that CD4+ T cells can combat tumours through a multitude of pathways.”
The detailed analysis revealed the genetic makeup, developmental states and functions of CD4+ T cells in melanoma, showing the potential of harnessing CD4+ T cells for future therapies against the skin cancer.
University of Melbourne Professor Thomas Gebhardt, Senior Research Fellow at the Doherty Institute and senior author of the study, said that understanding CD4+ T cell responses could pave the way for more effective immunotherapies against melanoma.
“While CD4+ T cells are often viewed as accessory cells regulating the function of other immune cells, our work shows they can work effectively on their own. Therefore, harnessing their potential therapeutically holds great promise for the development and improvement of current cancer immunotherapies,” said Professor Gebhardt.
More than 15,000 Australians are diagnosed with melanoma every year, a rare but highly aggressive form of skin cancer.
— ENDS
Additional information:
- Peer review: Bawden E, et al. CD4+ T cell immunity against cutaneous melanoma encompasses multifaceted responses. Science Immunology (2024). DOI: http://doi.org/10.1126/sciimmunol.adi9517
- Acknowledgements: The researchers thank the patients and families involved in this study for their contributions to this research.
- Collaboration: The researchers acknowledge that this work is the result of a collaboration between the Doherty Institute, the University of Bonn, the University of Sydney, the University of Melbourne, the Royal Prince Alfred Hospital, NSW Health Pathology, University of Maryland, the United States Department of Veterans Affairs, College Park, Marlene and Stewart Greenebaum Cancer Center, Peter MacCallum Cancer Centre, Telethon Kids Institute and the University of Western Australia.
- Funding: This research was supported by the National Health and Medical Research Council (NHMRC), Australia; Cancer Council Victoria, Australia; German Research Council, Germany; University of Melbourne, Australia; Deutsche Forschungsgemeinschaft (DFG; German Research Foundation), Germany; Cancer Council Western Australia, Australia; Peter MacCallum Cancer Foundation, Australia; University of Sydney, Australia; McMurtrie Cancer Pathology Fellowship, Australia; Melanoma Institute Australia, Australia; Cancer Institute NSW, Australia; Ainsworth Foundation, USA, The CLEARbridge Foundation, Australia; and the Cameron Family.
- Special note to journalists: More information, including a copy of the paper, can be found online in the Science Immunology press package at https://www.eurekalert.org/press/immunopak
About the Peter Doherty Institute for Infection and Immunity
Finding solutions to prevent, treat and cure infectious diseases and understanding the complexities of the immune system requires innovative approaches and concentrated effort. This is why The University of Melbourne – a world leader in education, teaching and research excellence – and The Royal Melbourne Hospital – an internationally renowned institution providing outstanding care, treatment and medical research – have partnered to create the Peter Doherty Institute for Infection and Immunity (Doherty Institute); a centre of excellence where leading scientists and clinicians collaborate to improve human health globally.
doherty.edu.au
Journal
Science Immunology
DOI
10.1126/sciimmunol.adi9517
Method of Research
Experimental study
Subject of Research
Animals
Article Title
CD4+ T cell immunity against cutaneous melanoma encompasses multifaceted responses
Article Publication Date
19-Jan-2024
COI Statement
T.G. is a scientific advisory board member of oNKo Innate Pty. Ltd. and
with S.B. has received research funding from Merck Healthcare KGaA. C.M.J. is an employee of
the VA Maryland Health Care System. The views reported in this paper do not reflect the views of
the Department of Veterans Affairs or the United States Government. C.M.J. has an equity position
with Cartesian Therapeutics. D.E.G. has received honoraria from Bristol Myers Squibb and Merck
Sharp & Dohme and is on an Advisory Board at Q Biotics, Provectus, Amgen, and Bayer. R.A.S.
has received fees for professional services from F. Hoffmann-La Roche Ltd., Evaxion, Provectus
Biopharmaceuticals Australia, Qbiotics, Novartis, Merck Sharp & Dohme, NeraCare, AMGEN
Inc., Bristol-Myers Squibb, Myriad Genetics, and GlaxoSmithKline. D.H. is currently an employee
of LAMPseq Diagnostics GmbH, Bonn, Germany. The other authors declare that they have no
competing interests.
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