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Complement in Kidney Transplantation

The complement system is considered to be an important part of innate immune system with a significant role in inflammation processes. The activation can occur through classical, alternative, or lectin pathway, resulting in the creation of anaphylatoxins C3a and C5a, possessing a vast spectrum of im...

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Detalles Bibliográficos
Autores principales: Cernoch, Marek, Viklicky, Ondrej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5447724/
https://www.ncbi.nlm.nih.gov/pubmed/28611987
http://dx.doi.org/10.3389/fmed.2017.00066
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author Cernoch, Marek
Viklicky, Ondrej
author_facet Cernoch, Marek
Viklicky, Ondrej
author_sort Cernoch, Marek
collection PubMed
description The complement system is considered to be an important part of innate immune system with a significant role in inflammation processes. The activation can occur through classical, alternative, or lectin pathway, resulting in the creation of anaphylatoxins C3a and C5a, possessing a vast spectrum of immune functions, and the assembly of terminal complement cascade, capable of direct cell lysis. The activation processes are tightly regulated; inappropriate activation of the complement cascade plays a significant role in many renal diseases including organ transplantation. Moreover, complement cascade is activated during ischemia/reperfusion injury processes and influences delayed graft function of kidney allografts. Interestingly, complement system has been found to play a role in both acute cellular and antibody-mediated rejections and thrombotic microangiopathy. Therefore, complement system may represent an interesting therapeutical target in kidney transplant pathologies.
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spelling pubmed-54477242017-06-13 Complement in Kidney Transplantation Cernoch, Marek Viklicky, Ondrej Front Med (Lausanne) Medicine The complement system is considered to be an important part of innate immune system with a significant role in inflammation processes. The activation can occur through classical, alternative, or lectin pathway, resulting in the creation of anaphylatoxins C3a and C5a, possessing a vast spectrum of immune functions, and the assembly of terminal complement cascade, capable of direct cell lysis. The activation processes are tightly regulated; inappropriate activation of the complement cascade plays a significant role in many renal diseases including organ transplantation. Moreover, complement cascade is activated during ischemia/reperfusion injury processes and influences delayed graft function of kidney allografts. Interestingly, complement system has been found to play a role in both acute cellular and antibody-mediated rejections and thrombotic microangiopathy. Therefore, complement system may represent an interesting therapeutical target in kidney transplant pathologies. Frontiers Media S.A. 2017-05-30 /pmc/articles/PMC5447724/ /pubmed/28611987 http://dx.doi.org/10.3389/fmed.2017.00066 Text en Copyright © 2017 Cernoch and Viklicky. http://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) or licensor 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 Medicine
Cernoch, Marek
Viklicky, Ondrej
Complement in Kidney Transplantation
title Complement in Kidney Transplantation
title_full Complement in Kidney Transplantation
title_fullStr Complement in Kidney Transplantation
title_full_unstemmed Complement in Kidney Transplantation
title_short Complement in Kidney Transplantation
title_sort complement in kidney transplantation
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5447724/
https://www.ncbi.nlm.nih.gov/pubmed/28611987
http://dx.doi.org/10.3389/fmed.2017.00066
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