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Complement-targeting therapeutics for ischemia-reperfusion injury in transplantation and the potential for ex vivo delivery
Organ shortages and an expanding waitlist have led to increased utilization of marginal organs. All donor organs are subject to varying degrees of IRI during the transplant process. Extended criteria organs, including those from older donors and organs donated after circulatory death are especially...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9626853/ https://www.ncbi.nlm.nih.gov/pubmed/36341433 http://dx.doi.org/10.3389/fimmu.2022.1000172 |
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author | Delaura, Isabel F. Gao, Qimeng Anwar, Imran J. Abraham, Nader Kahan, Riley Hartwig, Matthew G. Barbas, Andrew S. |
author_facet | Delaura, Isabel F. Gao, Qimeng Anwar, Imran J. Abraham, Nader Kahan, Riley Hartwig, Matthew G. Barbas, Andrew S. |
author_sort | Delaura, Isabel F. |
collection | PubMed |
description | Organ shortages and an expanding waitlist have led to increased utilization of marginal organs. All donor organs are subject to varying degrees of IRI during the transplant process. Extended criteria organs, including those from older donors and organs donated after circulatory death are especially vulnerable to ischemia-reperfusion injury (IRI). Involvement of the complement cascade in mediating IRI has been studied extensively. Complement plays a vital role in the propagation of IRI and subsequent recruitment of the adaptive immune elements. Complement inhibition at various points of the pathway has been shown to mitigate IRI and minimize future immune-mediated injury in preclinical models. The recent introduction of ex vivo machine perfusion platforms provides an ideal window for therapeutic interventions. Here we review the role of complement in IRI by organ system and highlight potential therapeutic targets for intervention during ex vivo machine preservation of donor organs. |
format | Online Article Text |
id | pubmed-9626853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96268532022-11-03 Complement-targeting therapeutics for ischemia-reperfusion injury in transplantation and the potential for ex vivo delivery Delaura, Isabel F. Gao, Qimeng Anwar, Imran J. Abraham, Nader Kahan, Riley Hartwig, Matthew G. Barbas, Andrew S. Front Immunol Immunology Organ shortages and an expanding waitlist have led to increased utilization of marginal organs. All donor organs are subject to varying degrees of IRI during the transplant process. Extended criteria organs, including those from older donors and organs donated after circulatory death are especially vulnerable to ischemia-reperfusion injury (IRI). Involvement of the complement cascade in mediating IRI has been studied extensively. Complement plays a vital role in the propagation of IRI and subsequent recruitment of the adaptive immune elements. Complement inhibition at various points of the pathway has been shown to mitigate IRI and minimize future immune-mediated injury in preclinical models. The recent introduction of ex vivo machine perfusion platforms provides an ideal window for therapeutic interventions. Here we review the role of complement in IRI by organ system and highlight potential therapeutic targets for intervention during ex vivo machine preservation of donor organs. Frontiers Media S.A. 2022-10-19 /pmc/articles/PMC9626853/ /pubmed/36341433 http://dx.doi.org/10.3389/fimmu.2022.1000172 Text en Copyright © 2022 Delaura, Gao, Anwar, Abraham, Kahan, Hartwig and Barbas https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Delaura, Isabel F. Gao, Qimeng Anwar, Imran J. Abraham, Nader Kahan, Riley Hartwig, Matthew G. Barbas, Andrew S. Complement-targeting therapeutics for ischemia-reperfusion injury in transplantation and the potential for ex vivo delivery |
title | Complement-targeting therapeutics for ischemia-reperfusion injury in transplantation and the potential for ex vivo delivery |
title_full | Complement-targeting therapeutics for ischemia-reperfusion injury in transplantation and the potential for ex vivo delivery |
title_fullStr | Complement-targeting therapeutics for ischemia-reperfusion injury in transplantation and the potential for ex vivo delivery |
title_full_unstemmed | Complement-targeting therapeutics for ischemia-reperfusion injury in transplantation and the potential for ex vivo delivery |
title_short | Complement-targeting therapeutics for ischemia-reperfusion injury in transplantation and the potential for ex vivo delivery |
title_sort | complement-targeting therapeutics for ischemia-reperfusion injury in transplantation and the potential for ex vivo delivery |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9626853/ https://www.ncbi.nlm.nih.gov/pubmed/36341433 http://dx.doi.org/10.3389/fimmu.2022.1000172 |
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