Stem-like T cells offer potential in treating cancer and chronic illnesses by targeting immune response.

Stem-like memory and precursors of exhausted T cells share a common progenitor defined by ID3 expression
Go to source). Published in Science Immunology, 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.
‘ID3+ #Tcells: The #immune system's marathon runners! They resist #burnout, maintaining a powerful response against #chronicinfections and #cancer. #worldcancerday’






ID3+ T Cells: Unlocking Long-Lasting Immune Response
The University of Melbourne’s Catarina Gago da Graça, 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.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.”
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“Exhausted immune cells remain one of the biggest challenges in treating chronic diseases,” said Dr Utzschneider.
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Reference:
- Stem-like memory and precursors of exhausted T cells share a common progenitor defined by ID3 expression - (https://www.science.org/doi/10.1126/sciimmunol.adn1945)
Source-Eurekalert