Impact of age on the homing potential of 89Zr-radiolabelled CD8 + T cells
Jonas Bystrom, Melissa Pereira Da Costa, Amaia Carrascal-Miniño, Ahad Qureshi, George P. Keeling, Truc T. Pham, Kavitha Sunassee, Elizabeth C. Carroll, Conor Garrod-Ketchley, Johannes Schroth, Victoria S. K. Tsang, Rafael T. M. de Rosales, Samantha Y. A. Terry, Sian M. Henson

TL;DR
This study shows that CD8+ T cells from older individuals move more slowly in the body and may cause more tissue damage compared to those from younger individuals.
Contribution
A method for radiolabelling and tracking cryopreserved CD8+ T cells in vivo using ⁸⁹Zr and PET imaging is established.
Findings
CD8+ T cells from older individuals migrate more slowly and accumulate in tissues later than those from younger individuals.
Aged T cells show decreased cortactin expression and increased cholesterol levels, which may impair their motility.
The study provides a framework for assessing age-related functional deficits in T cells using PET imaging.
Abstract
The ability of CD8 + T cells to protect against infections and malignant transformations declines with age. Emerging technologies, such as total body positron emission tomography (PET) and radiotracers with long half-lives, offer new approaches to assess long-term cellular functional deficits in vivo. In this study, we radiolabelled human CD8 + T cells from both young and old individuals with zirconium-89 (⁸⁹Zr) and evaluated their distribution in vivo. ⁸⁹Zr-labelled CD8 + T cells were injected intravenously into NOD scid gamma mice, and their whole-body migration was tracked using PET imaging. Longitudinal PET imaging revealed that CD8 + T cells from older individuals accumulated in tissues at a slower rate compared to those from younger individuals and may have caused greater tissue damage. This impaired migration was associated with decreased cortactin expression and increased…
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Taxonomy
TopicsCAR-T cell therapy research · Immunotherapy and Immune Responses · T-cell and B-cell Immunology
