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Immune characterization of a xenogeneic human lung cross-circulation support system

Improved approaches to expanding the pool of donor lungs suitable for transplantation are critically needed for the growing population with end-stage lung disease. Cross-circulation (XC) of whole blood between swine and explanted human lungs has previously been reported to enable the extracorporeal...

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Autores principales: Wu, Wei K., Stier, Matthew T., Stokes, John W., Ukita, Rei, Patel, Yatrik J., Cortelli, Michael, Landstreet, Stuart R., Talackine, Jennifer R., Cardwell, Nancy L., Simonds, Elizabeth M., Mentz, Meredith, Lowe, Cindy, Benson, Clayne, Demarest, Caitlin T., Alexopoulos, Sophoclis P., Shaver, Ciara M., Bacchetta, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10065447/
https://www.ncbi.nlm.nih.gov/pubmed/37000867
http://dx.doi.org/10.1126/sciadv.ade7647
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author Wu, Wei K.
Stier, Matthew T.
Stokes, John W.
Ukita, Rei
Patel, Yatrik J.
Cortelli, Michael
Landstreet, Stuart R.
Talackine, Jennifer R.
Cardwell, Nancy L.
Simonds, Elizabeth M.
Mentz, Meredith
Lowe, Cindy
Benson, Clayne
Demarest, Caitlin T.
Alexopoulos, Sophoclis P.
Shaver, Ciara M.
Bacchetta, Matthew
author_facet Wu, Wei K.
Stier, Matthew T.
Stokes, John W.
Ukita, Rei
Patel, Yatrik J.
Cortelli, Michael
Landstreet, Stuart R.
Talackine, Jennifer R.
Cardwell, Nancy L.
Simonds, Elizabeth M.
Mentz, Meredith
Lowe, Cindy
Benson, Clayne
Demarest, Caitlin T.
Alexopoulos, Sophoclis P.
Shaver, Ciara M.
Bacchetta, Matthew
author_sort Wu, Wei K.
collection PubMed
description Improved approaches to expanding the pool of donor lungs suitable for transplantation are critically needed for the growing population with end-stage lung disease. Cross-circulation (XC) of whole blood between swine and explanted human lungs has previously been reported to enable the extracorporeal recovery of donor lungs that declined for transplantation due to acute, reversible injuries. However, immunologic interactions of this xenogeneic platform have not been characterized, thus limiting potential translational applications. Using flow cytometry and immunohistochemistry, we demonstrate that porcine immune cell and immunoglobulin infiltration occurs in this xenogeneic XC system, in the context of calcineurin-based immunosuppression and complement depletion. Despite this, xenogeneic XC supported the viability, tissue integrity, and physiologic improvement of human donor lungs over 24 hours of xeno-support. These findings provide targets for future immunomodulatory strategies to minimize immunologic interactions on this organ support biotechnology.
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spelling pubmed-100654472023-04-01 Immune characterization of a xenogeneic human lung cross-circulation support system Wu, Wei K. Stier, Matthew T. Stokes, John W. Ukita, Rei Patel, Yatrik J. Cortelli, Michael Landstreet, Stuart R. Talackine, Jennifer R. Cardwell, Nancy L. Simonds, Elizabeth M. Mentz, Meredith Lowe, Cindy Benson, Clayne Demarest, Caitlin T. Alexopoulos, Sophoclis P. Shaver, Ciara M. Bacchetta, Matthew Sci Adv Biomedicine and Life Sciences Improved approaches to expanding the pool of donor lungs suitable for transplantation are critically needed for the growing population with end-stage lung disease. Cross-circulation (XC) of whole blood between swine and explanted human lungs has previously been reported to enable the extracorporeal recovery of donor lungs that declined for transplantation due to acute, reversible injuries. However, immunologic interactions of this xenogeneic platform have not been characterized, thus limiting potential translational applications. Using flow cytometry and immunohistochemistry, we demonstrate that porcine immune cell and immunoglobulin infiltration occurs in this xenogeneic XC system, in the context of calcineurin-based immunosuppression and complement depletion. Despite this, xenogeneic XC supported the viability, tissue integrity, and physiologic improvement of human donor lungs over 24 hours of xeno-support. These findings provide targets for future immunomodulatory strategies to minimize immunologic interactions on this organ support biotechnology. American Association for the Advancement of Science 2023-03-31 /pmc/articles/PMC10065447/ /pubmed/37000867 http://dx.doi.org/10.1126/sciadv.ade7647 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Wu, Wei K.
Stier, Matthew T.
Stokes, John W.
Ukita, Rei
Patel, Yatrik J.
Cortelli, Michael
Landstreet, Stuart R.
Talackine, Jennifer R.
Cardwell, Nancy L.
Simonds, Elizabeth M.
Mentz, Meredith
Lowe, Cindy
Benson, Clayne
Demarest, Caitlin T.
Alexopoulos, Sophoclis P.
Shaver, Ciara M.
Bacchetta, Matthew
Immune characterization of a xenogeneic human lung cross-circulation support system
title Immune characterization of a xenogeneic human lung cross-circulation support system
title_full Immune characterization of a xenogeneic human lung cross-circulation support system
title_fullStr Immune characterization of a xenogeneic human lung cross-circulation support system
title_full_unstemmed Immune characterization of a xenogeneic human lung cross-circulation support system
title_short Immune characterization of a xenogeneic human lung cross-circulation support system
title_sort immune characterization of a xenogeneic human lung cross-circulation support system
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10065447/
https://www.ncbi.nlm.nih.gov/pubmed/37000867
http://dx.doi.org/10.1126/sciadv.ade7647
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