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New Answers to Old Conundrums: What Antibodies, Exosomes and Inflammasomes Bring to the Conversation. Canadian National Transplant Research Program International Summit Report

Antibody-mediated injury is a major cause of allograft dysfunction and loss. Antibodies to ABH(O) blood group antigens are classic mediators of ABO-incompatible graft rejection, whereas donor-specific anti-HLA antibodies and, more recently, autoantibodies are appreciated as important contributors to...

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Autores principales: Dieudé, Mélanie, West, Lori J., Muruve, Daniel A., Gunaratman, Lakshman, Mohanakumar, Thalachallour, Zorn, Emmanuel, Cairo, Christopher W., Freed, Darren H., Schultz, Kirk R., Fairchild, Robert L., Hébert, Marie-Josée
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802265/
https://www.ncbi.nlm.nih.gov/pubmed/28731910
http://dx.doi.org/10.1097/TP.0000000000001872
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author Dieudé, Mélanie
West, Lori J.
Muruve, Daniel A.
Gunaratman, Lakshman
Mohanakumar, Thalachallour
Zorn, Emmanuel
Cairo, Christopher W.
Freed, Darren H.
Schultz, Kirk R.
Fairchild, Robert L.
Hébert, Marie-Josée
author_facet Dieudé, Mélanie
West, Lori J.
Muruve, Daniel A.
Gunaratman, Lakshman
Mohanakumar, Thalachallour
Zorn, Emmanuel
Cairo, Christopher W.
Freed, Darren H.
Schultz, Kirk R.
Fairchild, Robert L.
Hébert, Marie-Josée
author_sort Dieudé, Mélanie
collection PubMed
description Antibody-mediated injury is a major cause of allograft dysfunction and loss. Antibodies to ABH(O) blood group antigens are classic mediators of ABO-incompatible graft rejection, whereas donor-specific anti-HLA antibodies and, more recently, autoantibodies are appreciated as important contributors to allograft inflammation and dysfunction. In August 2016, the International Summit of the Canadian National Transplant Research Program focused on recent advances in the field of antibody-mediated rejection. Here, we describe work presented and discussed at the meeting, with a focus on 3 major themes: the importance of (1) natural antibodies and autoantibodies, (2) tissue injury–derived exosomes and autoimmunity, (3) inflammasome activation and innate immune responses in regulating allograft inflammation and dysfunction. Finally, we explore novel areas of therapeutic intervention that have recently emerged from these 3 major and overlapping fields of transplantation research.
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spelling pubmed-58022652018-02-13 New Answers to Old Conundrums: What Antibodies, Exosomes and Inflammasomes Bring to the Conversation. Canadian National Transplant Research Program International Summit Report Dieudé, Mélanie West, Lori J. Muruve, Daniel A. Gunaratman, Lakshman Mohanakumar, Thalachallour Zorn, Emmanuel Cairo, Christopher W. Freed, Darren H. Schultz, Kirk R. Fairchild, Robert L. Hébert, Marie-Josée Transplantation Reviews Antibody-mediated injury is a major cause of allograft dysfunction and loss. Antibodies to ABH(O) blood group antigens are classic mediators of ABO-incompatible graft rejection, whereas donor-specific anti-HLA antibodies and, more recently, autoantibodies are appreciated as important contributors to allograft inflammation and dysfunction. In August 2016, the International Summit of the Canadian National Transplant Research Program focused on recent advances in the field of antibody-mediated rejection. Here, we describe work presented and discussed at the meeting, with a focus on 3 major themes: the importance of (1) natural antibodies and autoantibodies, (2) tissue injury–derived exosomes and autoimmunity, (3) inflammasome activation and innate immune responses in regulating allograft inflammation and dysfunction. Finally, we explore novel areas of therapeutic intervention that have recently emerged from these 3 major and overlapping fields of transplantation research. Lippincott Williams & Wilkins 2018-02 2018-01-30 /pmc/articles/PMC5802265/ /pubmed/28731910 http://dx.doi.org/10.1097/TP.0000000000001872 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Reviews
Dieudé, Mélanie
West, Lori J.
Muruve, Daniel A.
Gunaratman, Lakshman
Mohanakumar, Thalachallour
Zorn, Emmanuel
Cairo, Christopher W.
Freed, Darren H.
Schultz, Kirk R.
Fairchild, Robert L.
Hébert, Marie-Josée
New Answers to Old Conundrums: What Antibodies, Exosomes and Inflammasomes Bring to the Conversation. Canadian National Transplant Research Program International Summit Report
title New Answers to Old Conundrums: What Antibodies, Exosomes and Inflammasomes Bring to the Conversation. Canadian National Transplant Research Program International Summit Report
title_full New Answers to Old Conundrums: What Antibodies, Exosomes and Inflammasomes Bring to the Conversation. Canadian National Transplant Research Program International Summit Report
title_fullStr New Answers to Old Conundrums: What Antibodies, Exosomes and Inflammasomes Bring to the Conversation. Canadian National Transplant Research Program International Summit Report
title_full_unstemmed New Answers to Old Conundrums: What Antibodies, Exosomes and Inflammasomes Bring to the Conversation. Canadian National Transplant Research Program International Summit Report
title_short New Answers to Old Conundrums: What Antibodies, Exosomes and Inflammasomes Bring to the Conversation. Canadian National Transplant Research Program International Summit Report
title_sort new answers to old conundrums: what antibodies, exosomes and inflammasomes bring to the conversation. canadian national transplant research program international summit report
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802265/
https://www.ncbi.nlm.nih.gov/pubmed/28731910
http://dx.doi.org/10.1097/TP.0000000000001872
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