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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2018
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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. |
format | Online Article Text |
id | pubmed-5802265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
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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