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Polymerized Human Hemoglobin-Based Oxygen Carrier Preserves Lung Allograft Function During Normothermic Ex Vivo Lung Perfusion.
Cuddington, Clayton; Greenfield, Alisyn; Lee, Yong Gyu; Kim, Jung Lye; Lamb, Derek; Buehler, Paul W; Black, Sylvester M; Palmer, Andre F; Whitson, Bryan A.
Afiliação
  • Cuddington C; From the William G. Lowrie Department of Chemical and Biomolecular Engineering, College of Engineering, The Ohio State University.
  • Greenfield A; From the William G. Lowrie Department of Chemical and Biomolecular Engineering, College of Engineering, The Ohio State University.
  • Lee YG; Department of Surgery, The Ohio State University Wexner Medical Center, Columbus, Ohio.
  • Kim JL; The Collaboration for Organ Perfusion, Preservation, Engineering and Regeneration (COPPER) Laboratory.
  • Lamb D; Department of Surgery, The Ohio State University Wexner Medical Center, Columbus, Ohio.
  • Buehler PW; The Collaboration for Organ Perfusion, Preservation, Engineering and Regeneration (COPPER) Laboratory.
  • Black SM; Departments of Pathology and Pediatrics, Center for Blood Oxygen Transport Hemostasis, University of Maryland School of Medicine, Baltimore, Maryland.
  • Palmer AF; Departments of Pathology and Pediatrics, Center for Blood Oxygen Transport Hemostasis, University of Maryland School of Medicine, Baltimore, Maryland.
  • Whitson BA; Department of Surgery, The Ohio State University Wexner Medical Center, Columbus, Ohio.
ASAIO J ; 70(5): 442-450, 2024 05 01.
Article em En | MEDLINE | ID: mdl-38266069
ABSTRACT
Normothermic ex vivo lung perfusion (EVLP) can resuscitate marginal lung allografts to increase organs available for transplantation. During normothermic perfusion, cellular metabolism is more active compared with subnormothermic perfusion, creating a need for an oxygen (O 2 ) carrier in the perfusate. As an O 2 carrier, red blood cells (RBCs) are a scarce resource and are susceptible to hemolysis in perfusion circuits, thus releasing cell-free hemoglobin (Hb), which can extravasate into the tissue space, thus promoting scavenging of nitric oxide (NO) and oxidative tissue damage. Fortunately, polymerized human Hb (PolyhHb) represents a synthetic O 2 carrier with a larger molecular diameter compared with Hb, preventing extravasation, and limiting adverse reactions. In this study, a next-generation PolyhHb-based perfusate was compared to both RBC and asanguinous perfusates in a rat EVLP model. During EVLP, the pulmonary arterial pressure and pulmonary vascular resistance were both significantly higher in lungs perfused with RBCs, which is consistent with RBC hemolysis. Lungs perfused with PolyhHb demonstrated greater oxygenation than those perfused with RBCs. Post-EVLP analysis revealed that the PolyhHb perfusate elicited less cellular damage, extravasation, iron tissue deposition, and edema than either RBCs or colloid control. These results show promise for a next-generation PolyhHb to maintain lung function throughout EVLP.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Perfusão / Substitutos Sanguíneos / Hemoglobinas / Transplante de Pulmão / Ratos Sprague-Dawley Limite: Animals / Humans / Male Idioma: En Revista: ASAIO J Assunto da revista: TRANSPLANTE Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Perfusão / Substitutos Sanguíneos / Hemoglobinas / Transplante de Pulmão / Ratos Sprague-Dawley Limite: Animals / Humans / Male Idioma: En Revista: ASAIO J Assunto da revista: TRANSPLANTE Ano de publicação: 2024 Tipo de documento: Article