Researchers have uncovered an incredible breakthrough in understanding how certain T cells can maintain powerful immune responses over time. By identifying a unique protein called ID3, scientists found that some immune cells can resist exhaustion and continue fighting chronic diseases effectively. This discovery could revolutionize treatments for cancer and persistent infections by potentially enhancing immune cell durability. The research offers a promising new approach to strengthening the body's natural defense mechanisms and improving long-term patient outcomes.
February 03, 2025
Research unlocks key to long-lasting immune response in cancer
"ID3+ T cells have the remarkable ability
to resist burnout and maintain a powerful immune response over time" -
Catarina Gago da Graca
Melbourne, February 1: Prolonged illnesses, such as cancer and persistent
infections, can fatigue the immune system, causing its frontline defenders, T
cells, to lose their ability to act efficiently.
Key Points
1 Stem-like T cells maintain
powerful long-term immune responses
2 ID3 protein enables T cells to
self-renew and resist exhaustion
3 Research could transform
immunotherapy and chronic disease treatment
4 Specific inflammatory signals
can promote immune cell formation
The Peter Doherty Institute for
Infection and Immunity (Doherty Institute) and the Peter MacCallum Cancer
Centre (Peter Mac) have discovered a unique type of immune cell known as
stem-like T cells, which is essential for maintaining potent, long-term immune
responses.
The study revealed that the
endurance of these stem-like T cells is fuelled by a protein called ID3,
expressed by a gene of the same name. These ID3+ T cells have a unique ability
to self-renew and resist exhaustion, giving them the power to sustain immune
responses far longer than other T cells that don't express ID3.
The University of Melbourne's
Catarina Gago da Graca, PhD Candidate at the Doherty Institute, said the
research highlights how ID3+ T cells hold the key to overcoming one of the
biggest challenges in treating chronic diseases--immune exhaustion.
"ID3+ T cells have the
remarkable ability to resist burnout and maintain a powerful immune response
over time, making them particularly effective in the face of chronic infections
or cancer," said co-first author Gago da Graca.
The research also found that
certain signals in the body could increase the number of ID3+ T cells, paving
the way for improved treatments like CAR T cell therapy. While CAR T therapy
has been transformative in treating certain cancers, its effectiveness can wane
over time due to T cell exhaustion.
Professor Ricky Johnstone,
Executive Director Cancer Research at Peter Mac and co-lead author of the
study, said enhancing ID3 activity could strengthen the endurance of these
cells, making therapies more effective and long-lasting.
"We discovered that ID3+ T
cell formation could be promoted by specific inflammatory cues, potentially
offering new strategies to boost the number of immune cells that excel at
fighting cancer in patients," said Professor Johnstone.
"This could lead to better
treatments for cancer patients and improve clinical immunotherapy
outcomes."
The University of Melbourne's Dr
Daniel Utzschneider, Laboratory Head at the Doherty Institute, said the
findings could lead to advancements in immunotherapy treatments and the
development of vaccines that provide long-lasting protection.
"Exhausted immune cells
remain one of the biggest challenges in treating chronic diseases," said
Dr Utzschneider.
"This research provides a
roadmap for how we might reinvigorate the immune system to improve health
outcomes for people living with cancer or chronic infections like HIV or
hepatitis B and C, thanks to these stem-like T cells, the immune system's
secret power."
This research is the result of a
collaborative effort between the Doherty Institute, Peter Mac, La Trobe
University, Northwestern University (USA), the Olivia Newton-John Cancer
Research Institute, the University of Birmingham (UK) and the University of
Melbourne.
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