» Articles » PMID: 39897527

Altered CD73-Adenosine Signaling Linked to Infection in Patients Undergoing Hemodialysis

Overview
Journal J Inflamm Res
Publisher Dove Medical Press
Date 2025 Feb 3
PMID 39897527
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: Infection is the most common cause of hospitalization and the second most common cause of mortality among patients undergoing hemodialysis (HD). The enzyme CD73, a cell surface 5'-nucleotidase, regulates the balance between pro-inflammatory nucleotides and anti-inflammatory adenosine. Diminished CD73-adenosine signaling contributes to severe infections.

Methods: In this prospective cohort study, 393 patients who underwent HD for over six months were evaluated for CD73Tcell ratios and were followed up for three years to track infection events. Kaplan-Meier curves and Cox regression analyses were used to evaluate the relationship between CD73T cells and infections; meanwhile, multiple logistic regression analysis was used to analyze differences among infection groups. In addition, a 5/6 nephrectomy (5/6 Nx) rat model and cecal ligation and puncture (CLP) were used to verify the effect of chronic kidney disease (CKD) and sepsis on CD73-adenosine signaling.

Results: Decreased CD73 T cells were independently associated with increased infection risk over one and three years. The hazard ratios for one- and three-year infection incidences were 3.173 (95% CI 1.782-5.650, p < 0.001) and 1.429 (95% CI 1.052-1.992, p = 0.035), respectively. Furthermore, they were associated with recurrent and fatal severe infections. Animal models demonstrated reduced CD73 mRNA transcript and adenosine receptor levels, along with decreased serum adenosine levels in CKD. Impairment of CD73-adenosine signaling was more pronounced after CLP in CKD rats.

Conclusion: Lower CD73T cell levels are strongly associated with infection complications in patients undergoing HD. Altered CD73-adenosine signaling likely plays a substantial role in immune dysfunction in CKD.

References
1.
Chen J, Li T, Huang D, Gong W, Tian J, Gao X . Integrating UHPLC-MS/MS quantitative analysis and exogenous purine supplementation to elucidate the antidepressant mechanism of Chaigui granules by regulating purine metabolism. J Pharm Anal. 2024; 13(12):1562-1576. PMC: 10785246. DOI: 10.1016/j.jpha.2023.08.008. View

2.
Betjes M, Langerak A, van der Spek A, de Wit E, Litjens N . Premature aging of circulating T cells in patients with end-stage renal disease. Kidney Int. 2011; 80(2):208-17. DOI: 10.1038/ki.2011.110. View

3.
Saravi N, Mousavi T . Seroprevalence of Cytomegalovirus antibodies and primary infection among hemodialysis patients: A systematic and meta-analysis review. Transpl Immunol. 2022; 72:101587. DOI: 10.1016/j.trim.2022.101587. View

4.
Cekic C, Linden J . Purinergic regulation of the immune system. Nat Rev Immunol. 2016; 16(3):177-92. DOI: 10.1038/nri.2016.4. View

5.
Wichterman K, Baue A, Chaudry I . Sepsis and septic shock--a review of laboratory models and a proposal. J Surg Res. 1980; 29(2):189-201. DOI: 10.1016/0022-4804(80)90037-2. View