Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024 Dec 11:12:1505601.
doi: 10.3389/fcell.2024.1505601. eCollection 2024.

Cell therapy in kidney diseases: advancing treatments for renal regeneration

Affiliations
Review

Cell therapy in kidney diseases: advancing treatments for renal regeneration

Amankeldi A Salybekov et al. Front Cell Dev Biol. .

Abstract

Kidney diseases, including acute kidney injury (AKI) and chronic kidney disease (CKD), pose a significant global health challenge, with high morbidity and mortality rates driven by rising prevalence of risk factors such as diabetes and hypertension. Current therapeutic strategies are often limited, prompting the exploration of advanced cell therapies as potential solutions. This review provides a comprehensive overview of the state of cell therapies in kidney disease, tracing the progression from preclinical studies to clinical applications. Recent studies highlited that cell-based interventions offer kidney-protective properties through mechanisms such as paracrine signaling, immune modulation, and direct tissue integration, demonstrating potential in both AKI and CKD settings. Despite promising results, challenges remain in optimizing cell therapy protocols, including cell sourcing, delivery methods, and long-term outcomes. Finally, the review addresses on efforts to enhance cell function, optimize dosing, and refine delivery techniques to improve clinical outcomes in kidney disease management.

Keywords: CD34 cells; acute kidney injury; cell therapy; chronic kidney diseases; kidney diseases; mesenchimal stem cells.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
An extracorporeal circuit equipped with the integrated SBI-101 system. Created in BioRender
FIGURE 2
FIGURE 2
Renal autologus cell therapy. Created in BioRender

Similar articles

Cited by

References

    1. Abdala P. M., Swanson E. A., Hutchens M. P. (2021). Meta-analysis of AKI to CKD transition in perioperative patients. Perioper. Med. Lond. Engl. 10, 24. 10.1186/s13741-021-00192-6 - DOI - PMC - PubMed
    1. Bonventre J. V., Yang L. (2011). Cellular pathophysiology of ischemic acute kidney injury. J. Clin. Investigation 121, 4210–4221. 10.1172/JCI45161 - DOI - PMC - PubMed
    1. Brasile L., Henry N., Orlando G., Stubenitsky B. (2019). Potentiating renal regeneration using mesenchymal stem cells. Transplantation 103, 307–313. 10.1097/TP.0000000000002455 - DOI - PMC - PubMed
    1. Brosnahan G., et al. (2021). Cell therapy for kidney diseases: advances and future directions. Front. Cell Biol. Dev. 10.3389/fcell.2021.685428 - DOI
    1. Burger D., Viñas J. L., Akbari S., Dehak H., Knoll W., Gutsol A., et al. (2015). Human endothelial colony-forming cells protect against acute kidney injury: role of exosomes. Am. J. Pathology 185, 2309–2323. 10.1016/j.ajpath.2015.04.010 - DOI - PubMed

LinkOut - more resources