Evidence for the important role of inflammation in xenotransplantation

Abstract There is increasing evidence of a sustained state of systemic inflammation after pig-to-nonhuman primate (NHP) xenotransplantation (that has been termed systemic inflammation in xenograft recipients [SIXR]). Increases in inflammatory markers, e.g., C-reactive protein, histones, serum amyloi...

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Main Authors: Juan Li, Hidetaka Hara, Yi Wang, Charles Esmon, David K. C. Cooper, Hayato Iwase
Format: Article
Language:English
Published: BMC 2019-05-01
Series:Journal of Inflammation
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12950-019-0213-3
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spelling doaj-79fc7a6cc60c4abf9cde721ef4378b762020-11-25T03:53:09ZengBMCJournal of Inflammation1476-92552019-05-0116111610.1186/s12950-019-0213-3Evidence for the important role of inflammation in xenotransplantationJuan Li0Hidetaka Hara1Yi Wang2Charles Esmon3David K. C. Cooper4Hayato Iwase5Second Affiliated Hospital, University of South ChinaXenotransplantation Program, Department of Surgery, University of Alabama at BirminghamSecond Affiliated Hospital, University of South ChinaCoagulation Biology Laboratory, Oklahoma Medical Research FoundationXenotransplantation Program, Department of Surgery, University of Alabama at BirminghamXenotransplantation Program, Department of Surgery, University of Alabama at BirminghamAbstract There is increasing evidence of a sustained state of systemic inflammation after pig-to-nonhuman primate (NHP) xenotransplantation (that has been termed systemic inflammation in xenograft recipients [SIXR]). Increases in inflammatory markers, e.g., C-reactive protein, histones, serum amyloid A, D-dimer, cytokines, chemokines, and a decrease in free triiodothyronine, have been demonstrated in the recipient NHPs. The complex interactions between inflammation, coagulation, and the immune response are well-recognized, but the role of inflammation in xenograft recipients is not fully understood. The evidence suggests that inflammation can promote the activation of coagulation and the adaptive immune response, but the exact mechanisms remain uncertain. If prolonged xenograft survival is to be achieved, anti-inflammatory strategies (e.g., the administration of anti-inflammatory agents, and/or the generation of genetically-engineered organ-source pigs that are protected from the effect of inflammation) may be necessary to prevent, control, or negate the effect of the systemic inflammation that develops in xenograft recipients. This may allow for a reduction in the intensity of exogenous immunosuppressive therapy. If immunological tolerance to a xenograft is to be obtained, then control of inflammation may be essential.http://link.springer.com/article/10.1186/s12950-019-0213-3InflammationNon-human primatesPigsXenotransplantation
collection DOAJ
language English
format Article
sources DOAJ
author Juan Li
Hidetaka Hara
Yi Wang
Charles Esmon
David K. C. Cooper
Hayato Iwase
spellingShingle Juan Li
Hidetaka Hara
Yi Wang
Charles Esmon
David K. C. Cooper
Hayato Iwase
Evidence for the important role of inflammation in xenotransplantation
Journal of Inflammation
Inflammation
Non-human primates
Pigs
Xenotransplantation
author_facet Juan Li
Hidetaka Hara
Yi Wang
Charles Esmon
David K. C. Cooper
Hayato Iwase
author_sort Juan Li
title Evidence for the important role of inflammation in xenotransplantation
title_short Evidence for the important role of inflammation in xenotransplantation
title_full Evidence for the important role of inflammation in xenotransplantation
title_fullStr Evidence for the important role of inflammation in xenotransplantation
title_full_unstemmed Evidence for the important role of inflammation in xenotransplantation
title_sort evidence for the important role of inflammation in xenotransplantation
publisher BMC
series Journal of Inflammation
issn 1476-9255
publishDate 2019-05-01
description Abstract There is increasing evidence of a sustained state of systemic inflammation after pig-to-nonhuman primate (NHP) xenotransplantation (that has been termed systemic inflammation in xenograft recipients [SIXR]). Increases in inflammatory markers, e.g., C-reactive protein, histones, serum amyloid A, D-dimer, cytokines, chemokines, and a decrease in free triiodothyronine, have been demonstrated in the recipient NHPs. The complex interactions between inflammation, coagulation, and the immune response are well-recognized, but the role of inflammation in xenograft recipients is not fully understood. The evidence suggests that inflammation can promote the activation of coagulation and the adaptive immune response, but the exact mechanisms remain uncertain. If prolonged xenograft survival is to be achieved, anti-inflammatory strategies (e.g., the administration of anti-inflammatory agents, and/or the generation of genetically-engineered organ-source pigs that are protected from the effect of inflammation) may be necessary to prevent, control, or negate the effect of the systemic inflammation that develops in xenograft recipients. This may allow for a reduction in the intensity of exogenous immunosuppressive therapy. If immunological tolerance to a xenograft is to be obtained, then control of inflammation may be essential.
topic Inflammation
Non-human primates
Pigs
Xenotransplantation
url http://link.springer.com/article/10.1186/s12950-019-0213-3
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AT charlesesmon evidencefortheimportantroleofinflammationinxenotransplantation
AT davidkccooper evidencefortheimportantroleofinflammationinxenotransplantation
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