Anti-uPAR CAR T cells reverse and prevent aging-associated defects in intestinal regeneration and fitness

Intestinal stem cells (ISCs) drive the rapid regeneration of the gut epithelium. However, during aging, their regenerative capacity wanes, possibly through senescence and chronic inflammation, albeit little is known about how aging-associated dysfunction arises in the intestine. We previously identified the urokinase plasminogen activator receptor (uPAR) as a senescence-associated protein and developed CAR T cells able to efficiently target it. Harnessing them, here, we identify the accumulation of mostly epithelial uPAR-positive cells in the aging gut and uncover their detrimental impact on ISC function in aging. Thus, both therapeutic and prophylactic treatment with anti-uPAR CAR T cells improved barrier function, regenerative capacity, inflammation, mucosal immune function and microbiome composition in aged mice. Overall, these findings reveal the deleterious role of uPAR-positive cells on intestinal aging in vivo and provide proof of concept for the potential of targeted immune-based cell therapies to enhance tissue regeneration in aging organisms.

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Publication Details

Journal
Nature Aging
Published
2025-11-25
DOI
https://doi.org/10.1038/s43587-025-01022-w
Citations
7
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
7.32
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article

Anti-uPAR CAR T cells reverse and prevent aging-associated defects in intestinal regeneration and fitness

Jill Habel, Semir Beyaz, Erdogan Oguzhan Akyildiz, Scott W. Lowe et al.
7 citations
Nature Aging
CAR-T cell therapy research
7.32
article

Anti-uPAR CAR T cells reverse and prevent aging-associated defects in intestinal regeneration and fitness

Jill Habel, Semir Beyaz, Erdogan Oguzhan Akyildiz, Scott W. Lowe, Ross L. Levine, Guangran Guo, Emmanuella Nnuji-John, Inés Fernández-Maestre, Saria Chowdhury, Aveline A. Filliol, Adam W. Anderson, Raditya Utama, Paul Bernard Romesser, Charlie Chung, Michel Sadelain, James Rouse, Corina Amor, Vyom Shah, Jacob A. Boyer, Onur Eskiocak, Alexander S. Harris, S. Flowers, Carolina Castro-Hernández, Joseph Gewolb
article en
7 citations

Abstract

Intestinal stem cells (ISCs) drive the rapid regeneration of the gut epithelium. However, during aging, their regenerative capacity wanes, possibly through senescence and chronic inflammation, albeit little is known about how aging-associated dysfunction arises in the intestine. We previously identified the urokinase plasminogen activator receptor (uPAR) as a senescence-associated protein and developed CAR T cells able to efficiently target it. Harnessing them, here, we identify the accumulation of mostly epithelial uPAR-positive cells in the aging gut and uncover their detrimental impact on ISC function in aging. Thus, both therapeutic and prophylactic treatment with anti-uPAR CAR T cells improved barrier function, regenerative capacity, inflammation, mucosal immune function and microbiome composition in aged mice. Overall, these findings reveal the deleterious role of uPAR-positive cells on intestinal aging in vivo and provide proof of concept for the potential of targeted immune-based cell therapies to enhance tissue regeneration in aging organisms.

Nature AgingVol. 6(1)
Rutgers, The State University of New Jersey (US), Memorial Sloan Kettering Cancer Center (US), Howard Hughes Medical Institute (US), Princeton University (US), Cornell University (US), Cold Spring Harbor Laboratory (US), Columbia University Irving Medical Center (US), Kent Hastanesi (TR), Ludwig Cancer Research (US), Acıbadem Adana Hospital (TR), Rutgers New Jersey Medical School (US), Stony Brook University (US)
Openalex Percentile: Top 2%
CAR-T cell therapy research
7.32
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