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CD16+ Monocytes and Skewed Macrophage Polarization toward M2 Type Hallmark Heart Transplant Acute Cellular Rejection

BACKGROUND: During acute heart transplant rejection, infiltration of lymphocytes and monocytes is followed by endothelial injury and eventually myocardial fibrosis. To date, no information is available on monocyte–macrophage-related cellular shifts and their polarization status during rejection. Her...

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Autores principales: van den Bosch, Thierry P. P., Caliskan, Kadir, Kraaij, Marina D., Constantinescu, Alina A., Manintveld, Olivier C., Leenen, Pieter J. M., von der Thüsen, Jan H., Clahsen-van Groningen, Marian C., Baan, Carla C., Rowshani, Ajda T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364145/
https://www.ncbi.nlm.nih.gov/pubmed/28392789
http://dx.doi.org/10.3389/fimmu.2017.00346
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author van den Bosch, Thierry P. P.
Caliskan, Kadir
Kraaij, Marina D.
Constantinescu, Alina A.
Manintveld, Olivier C.
Leenen, Pieter J. M.
von der Thüsen, Jan H.
Clahsen-van Groningen, Marian C.
Baan, Carla C.
Rowshani, Ajda T.
author_facet van den Bosch, Thierry P. P.
Caliskan, Kadir
Kraaij, Marina D.
Constantinescu, Alina A.
Manintveld, Olivier C.
Leenen, Pieter J. M.
von der Thüsen, Jan H.
Clahsen-van Groningen, Marian C.
Baan, Carla C.
Rowshani, Ajda T.
author_sort van den Bosch, Thierry P. P.
collection PubMed
description BACKGROUND: During acute heart transplant rejection, infiltration of lymphocytes and monocytes is followed by endothelial injury and eventually myocardial fibrosis. To date, no information is available on monocyte–macrophage-related cellular shifts and their polarization status during rejection. Here, we aimed to define and correlate monocyte–macrophage endomyocardial tissue profiles obtained at rejection and time points prior to rejection, with corresponding serial blood samples in 25 heart transplant recipients experiencing acute cellular rejection. Additionally, 33 healthy individuals served as control. MATERIALS AND METHODS: Using histology, immunohistochemistry, confocal laser scan microscopy, and digital imaging expression of CD14, CD16, CD56, CD68, CD80, and CD163 were explored to define monocyte and macrophage tissue profiles during rejection. Fibrosis was investigated using Sirius Red stainings of rejection, non-rejection, and 1-year biopsies. Expression of co-stimulatory and migration-related molecules on circulating monocytes, and production potential for pro- and anti-inflammatory cytokines were studied using flow cytometry. RESULTS: At tissue level, striking CD16+ monocyte infiltration was observed during rejection (p < 0.001). Significantly more CD68+CD163+ M2 macrophages were documented during rejection compared to barely present CD68+CD80+ M1 macrophages. Rejection was associated with severe fibrosis in 1-year biopsies (p < 0.001). Irrespective of rejection status, decreased frequencies of circulating CD16+ monocytes were found in patients compared to healthy individuals. Rejection was reflected by significantly increased CD54 and HLA-DR expression on CD16+ monocytes with retained cytokine production potential. CONCLUSION: CD16+ monocytes and M2 macrophages hallmark the correlates of heart transplant acute cellular rejection on tissue level and seem to be associated with fibrosis in the long term.
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spelling pubmed-53641452017-04-07 CD16+ Monocytes and Skewed Macrophage Polarization toward M2 Type Hallmark Heart Transplant Acute Cellular Rejection van den Bosch, Thierry P. P. Caliskan, Kadir Kraaij, Marina D. Constantinescu, Alina A. Manintveld, Olivier C. Leenen, Pieter J. M. von der Thüsen, Jan H. Clahsen-van Groningen, Marian C. Baan, Carla C. Rowshani, Ajda T. Front Immunol Immunology BACKGROUND: During acute heart transplant rejection, infiltration of lymphocytes and monocytes is followed by endothelial injury and eventually myocardial fibrosis. To date, no information is available on monocyte–macrophage-related cellular shifts and their polarization status during rejection. Here, we aimed to define and correlate monocyte–macrophage endomyocardial tissue profiles obtained at rejection and time points prior to rejection, with corresponding serial blood samples in 25 heart transplant recipients experiencing acute cellular rejection. Additionally, 33 healthy individuals served as control. MATERIALS AND METHODS: Using histology, immunohistochemistry, confocal laser scan microscopy, and digital imaging expression of CD14, CD16, CD56, CD68, CD80, and CD163 were explored to define monocyte and macrophage tissue profiles during rejection. Fibrosis was investigated using Sirius Red stainings of rejection, non-rejection, and 1-year biopsies. Expression of co-stimulatory and migration-related molecules on circulating monocytes, and production potential for pro- and anti-inflammatory cytokines were studied using flow cytometry. RESULTS: At tissue level, striking CD16+ monocyte infiltration was observed during rejection (p < 0.001). Significantly more CD68+CD163+ M2 macrophages were documented during rejection compared to barely present CD68+CD80+ M1 macrophages. Rejection was associated with severe fibrosis in 1-year biopsies (p < 0.001). Irrespective of rejection status, decreased frequencies of circulating CD16+ monocytes were found in patients compared to healthy individuals. Rejection was reflected by significantly increased CD54 and HLA-DR expression on CD16+ monocytes with retained cytokine production potential. CONCLUSION: CD16+ monocytes and M2 macrophages hallmark the correlates of heart transplant acute cellular rejection on tissue level and seem to be associated with fibrosis in the long term. Frontiers Media S.A. 2017-03-24 /pmc/articles/PMC5364145/ /pubmed/28392789 http://dx.doi.org/10.3389/fimmu.2017.00346 Text en Copyright © 2017 van den Bosch, Caliskan, Kraaij, Constantinescu, Manintveld, Leenen, von der Thüsen, Clahsen-van Groningen, Baan and Rowshani. 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 Immunology
van den Bosch, Thierry P. P.
Caliskan, Kadir
Kraaij, Marina D.
Constantinescu, Alina A.
Manintveld, Olivier C.
Leenen, Pieter J. M.
von der Thüsen, Jan H.
Clahsen-van Groningen, Marian C.
Baan, Carla C.
Rowshani, Ajda T.
CD16+ Monocytes and Skewed Macrophage Polarization toward M2 Type Hallmark Heart Transplant Acute Cellular Rejection
title CD16+ Monocytes and Skewed Macrophage Polarization toward M2 Type Hallmark Heart Transplant Acute Cellular Rejection
title_full CD16+ Monocytes and Skewed Macrophage Polarization toward M2 Type Hallmark Heart Transplant Acute Cellular Rejection
title_fullStr CD16+ Monocytes and Skewed Macrophage Polarization toward M2 Type Hallmark Heart Transplant Acute Cellular Rejection
title_full_unstemmed CD16+ Monocytes and Skewed Macrophage Polarization toward M2 Type Hallmark Heart Transplant Acute Cellular Rejection
title_short CD16+ Monocytes and Skewed Macrophage Polarization toward M2 Type Hallmark Heart Transplant Acute Cellular Rejection
title_sort cd16+ monocytes and skewed macrophage polarization toward m2 type hallmark heart transplant acute cellular rejection
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364145/
https://www.ncbi.nlm.nih.gov/pubmed/28392789
http://dx.doi.org/10.3389/fimmu.2017.00346
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