TY - JOUR
T1 - Theranostic methodology for ex vivo donor lung rehabilitation
AU - Pinezich, Meghan R.
AU - O'Neill, John D.
AU - Guenthart, Brandon A.
AU - Kim, Jinho
AU - Vila, Olaia F.
AU - Ma, Stephen P.
AU - Chen, Ya Wen
AU - Hozain, Ahmed E.
AU - Krishnan, Aravind
AU - Fawad, Moeed
AU - Cunningham, Katherine M.
AU - Wobma, Holly M.
AU - Van Hassel, Julie
AU - Snoeck, Hans Willem
AU - Bacchetta, Matthew
AU - Vunjak-Novakovic, Gordana
N1 - Publisher Copyright:
© 2025
PY - 2025/7/11
Y1 - 2025/7/11
N2 - Background: About 80% of donor lungs are not utilized for transplantation. Cross-circulation of ex vivo lungs with a support swine enables the rehabilitation of donor lungs that are initially deemed unsuitable for transplantation. Robust therapeutic and diagnostic modalities are needed for ex vivo lung rehabilitation; however, no standardized “theranostic” methodology has been reported. Methods: Ex vivo lungs (n = 23; 17 injured and 6 controls) with multi-focal contusion (n = 6, human), gastric aspiration injury (n = 8, swine), ischemia-reperfusion injury (n = 3, swine), or no injury (n = 6, swine) were used to develop a therapeutic and diagnostic (theranostic) methodology for ex vivo lung rehabilitation during cross-circulation. Airway (bronchoscopic, nebulized), intravascular, and transpleural access enabled sample collection and therapeutic delivery. Diagnostic modalities included non-invasive imaging, functional testing, and molecular assays. Therapeutic modalities included bronchoalveolar lavage, surfactant replacement, recruitment maneuvers, and cell/organoid delivery. Real-time tracking of delivered cells was performed via fluorescence and bioluminescence imaging. Findings: Diagnostic assessments revealed tissue-, cell-, and molecular-level insights at global and regional scales of ex vivo lungs during cross-circulation, which informed therapeutic management and interventions to recover donor lungs. Mesenchymal stromal cells and lung organoids were delivered bronchoscopically and transpleurally, tracked non-invasively during cross-circulation, and observed to localize within the parenchyma. Conclusions: Application of a theranostic methodology during cross-circulation enabled real-time ex vivo lung assessment and rehabilitation across a variety of lung injuries to help increase clinical utilization of donor lungs in the future. Funding: NIH (P41 EB027062, R01HL120046, U01HL134760), CFF (VUNJAK23XX0).
AB - Background: About 80% of donor lungs are not utilized for transplantation. Cross-circulation of ex vivo lungs with a support swine enables the rehabilitation of donor lungs that are initially deemed unsuitable for transplantation. Robust therapeutic and diagnostic modalities are needed for ex vivo lung rehabilitation; however, no standardized “theranostic” methodology has been reported. Methods: Ex vivo lungs (n = 23; 17 injured and 6 controls) with multi-focal contusion (n = 6, human), gastric aspiration injury (n = 8, swine), ischemia-reperfusion injury (n = 3, swine), or no injury (n = 6, swine) were used to develop a therapeutic and diagnostic (theranostic) methodology for ex vivo lung rehabilitation during cross-circulation. Airway (bronchoscopic, nebulized), intravascular, and transpleural access enabled sample collection and therapeutic delivery. Diagnostic modalities included non-invasive imaging, functional testing, and molecular assays. Therapeutic modalities included bronchoalveolar lavage, surfactant replacement, recruitment maneuvers, and cell/organoid delivery. Real-time tracking of delivered cells was performed via fluorescence and bioluminescence imaging. Findings: Diagnostic assessments revealed tissue-, cell-, and molecular-level insights at global and regional scales of ex vivo lungs during cross-circulation, which informed therapeutic management and interventions to recover donor lungs. Mesenchymal stromal cells and lung organoids were delivered bronchoscopically and transpleurally, tracked non-invasively during cross-circulation, and observed to localize within the parenchyma. Conclusions: Application of a theranostic methodology during cross-circulation enabled real-time ex vivo lung assessment and rehabilitation across a variety of lung injuries to help increase clinical utilization of donor lungs in the future. Funding: NIH (P41 EB027062, R01HL120046, U01HL134760), CFF (VUNJAK23XX0).
KW - Pre-clinical research
KW - cell therapy
KW - cross-circulation
KW - diagnostic
KW - donor lung rehabilitation
KW - ex vivo lung perfusion
KW - lung organoids
KW - lung transplantation
KW - mesenchymal stromal cells
KW - theranostic
KW - xenogeneic
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U2 - 10.1016/j.medj.2025.100644
DO - 10.1016/j.medj.2025.100644
M3 - Article
C2 - 40154476
AN - SCOPUS:105002662526
SN - 2666-6359
VL - 6
JO - Med
JF - Med
IS - 7
M1 - 100644
ER -