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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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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. |
format | Online Article Text |
id | pubmed-10065447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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