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Optimized cellular perfusate increases lung viability ex vivo and extends the duration of ex vivo lung perfusion.

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Arnold, CJ; Nakata, K; Hassan, A; Alderete, I; Aykun, N; Abraham, N; Carney, J; Xiang, Y; Kamaleswaran, R; Jiang, H; Hughes, BA; Barbas, AS ...
Published in: J Heart Lung Transplant
May 14, 2026

BACKGROUND: Ex vivo lung perfusion (EVLP) has emerged as a strategy to assess and extend preservation of donor lungs prior to transplantation. However, due to progressive deterioration of the graft, current protocols limit EVLP duration to 10-12 h. We developed an optimized cellular perfusate, DEVOL solution, designed to support multi-day EVLP and evaluated its performance against standard TransMedics OCS perfusate. METHODS: Porcine lungs were procured, flushed with OCS solution, and perfused using either STANDARD (n=5) or DEVOL (n=5) perfusate supplemented with washed red blood cells. Physiological parameters, perfusate biomarkers, histology, and transcriptomics were assessed throughout extended perfusion. A lung tissue culture system was employed to investigate procurement flush perfusate reperfusion-related cytokine release. RESULTS: DEVOL-perfused lungs exhibited increased median perfusion survival time compared with STANDARD (36 vs. 12 h). Improved viability was associated with reduced edema and lower endothelial injury markers (PECAM-1, syndecan-1). DEVOL lungs demonstrated transient early rises in pulmonary vascular resistance and IL-10, as well as sustained elevations in IL-17, without evidence of increased tissue injury. Mathematical simulation and cell culture experiments suggest this phenomenon is due in part to rapid calcium influx into DEVOL-perfused lungs following calcium-free OCS flush during procurement. CONCLUSION: DEVOL perfusate markedly prolongs lung viability during EVLP compared to standard, commercially available perfusate by maintaining oncotic and osmotic balance. Ongoing studies will dissect the contribution of individual DEVOL components to extended perfusion and integrate additional EVLP parameters to elucidate mechanisms underlying late graft failure observed in this study.

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Published In

J Heart Lung Transplant

DOI

EISSN

1557-3117

Publication Date

May 14, 2026

Location

United States

Related Subject Headings

  • Surgery
  • 3202 Clinical sciences
  • 3201 Cardiovascular medicine and haematology
 

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Arnold, C. J., Nakata, K., Hassan, A., Alderete, I., Aykun, N., Abraham, N., … Hartwig, M. G. (2026). Optimized cellular perfusate increases lung viability ex vivo and extends the duration of ex vivo lung perfusion. In J Heart Lung Transplant. United States. https://doi.org/10.1016/j.healun.2026.05.005
Arnold, C. J., K. Nakata, A. Hassan, I. Alderete, N. Aykun, N. Abraham, J. Carney, et al. “Optimized cellular perfusate increases lung viability ex vivo and extends the duration of ex vivo lung perfusion.” In J Heart Lung Transplant, 2026. https://doi.org/10.1016/j.healun.2026.05.005.
Arnold CJ, Nakata K, Hassan A, Alderete I, Aykun N, Abraham N, et al. Optimized cellular perfusate increases lung viability ex vivo and extends the duration of ex vivo lung perfusion. In: J Heart Lung Transplant. 2026.
Arnold, C. J., et al. “Optimized cellular perfusate increases lung viability ex vivo and extends the duration of ex vivo lung perfusion.J Heart Lung Transplant, 2026. Pubmed, doi:10.1016/j.healun.2026.05.005.
Arnold CJ, Nakata K, Hassan A, Alderete I, Aykun N, Abraham N, Carney J, Xiang Y, Kamaleswaran R, Jiang H, Hughes BA, Barbas AS, Hartwig MG. Optimized cellular perfusate increases lung viability ex vivo and extends the duration of ex vivo lung perfusion. J Heart Lung Transplant. 2026.
Journal cover image

Published In

J Heart Lung Transplant

DOI

EISSN

1557-3117

Publication Date

May 14, 2026

Location

United States

Related Subject Headings

  • Surgery
  • 3202 Clinical sciences
  • 3201 Cardiovascular medicine and haematology