Ultrastructural changes in acute lung allograft rejection: Novel insights from an animal study

Background Acute rejection (AR) episodes after lung transplantation (Tx) are orchestrated by cells of the innate and adaptive immune system targeting the engrafted organ. The assessment and classification of pathologic changes of AR relies essentially on conventional histology. Herein we apply the t...

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Veröffentlicht in:The Journal of heart and lung transplantation 2012, Vol.31 (1), p.94-100
Hauptverfasser: Jungraithmayr, Wolfgang, MD, Draenert, Alice, MD, Marquardt, Klaus, Weder, Walter, MD
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container_issue 1
container_start_page 94
container_title The Journal of heart and lung transplantation
container_volume 31
creator Jungraithmayr, Wolfgang, MD
Draenert, Alice, MD
Marquardt, Klaus
Weder, Walter, MD
description Background Acute rejection (AR) episodes after lung transplantation (Tx) are orchestrated by cells of the innate and adaptive immune system targeting the engrafted organ. The assessment and classification of pathologic changes of AR relies essentially on conventional histology. Herein we apply the technique of scanning electron microscopy (SEM) to identify and characterize ultrastructural changes of the pulmonary graft after lung Tx. Methods Orthotopic single-lung Tx was performed between BALB/c (donor) and C57BL/6 (recipient) mice. At Day 5 after Tx, lung allografts were recovered for SEM and for histologic analysis. Results Upon Tx, high numbers of leukocytes and thrombocytes were found, showing an activated surface pattern and a change of their cell body shape. These cells adhered and partly transmigrated through the endothelium of vessels. Larger vessels were more affected than smaller vessels and the endothelium was roughened in its surface texture throughout. As a phenomenon, airways were partly covered by activated dendritic cells. Numerous thrombocytes and macrophages accumulated on the endothelium of the cuff anastomosis region exposing this area to a particularly higher risk of thrombosis. Conclusions SEM allows for detection of morphologic changes during pulmonary allograft rejection and adds important data to conventional histology when making the diagnosis of acute rejection.
doi_str_mv 10.1016/j.healun.2011.10.003
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The assessment and classification of pathologic changes of AR relies essentially on conventional histology. Herein we apply the technique of scanning electron microscopy (SEM) to identify and characterize ultrastructural changes of the pulmonary graft after lung Tx. Methods Orthotopic single-lung Tx was performed between BALB/c (donor) and C57BL/6 (recipient) mice. At Day 5 after Tx, lung allografts were recovered for SEM and for histologic analysis. Results Upon Tx, high numbers of leukocytes and thrombocytes were found, showing an activated surface pattern and a change of their cell body shape. These cells adhered and partly transmigrated through the endothelium of vessels. Larger vessels were more affected than smaller vessels and the endothelium was roughened in its surface texture throughout. As a phenomenon, airways were partly covered by activated dendritic cells. Numerous thrombocytes and macrophages accumulated on the endothelium of the cuff anastomosis region exposing this area to a particularly higher risk of thrombosis. Conclusions SEM allows for detection of morphologic changes during pulmonary allograft rejection and adds important data to conventional histology when making the diagnosis of acute rejection.</description><identifier>ISSN: 1053-2498</identifier><identifier>EISSN: 1557-3117</identifier><identifier>DOI: 10.1016/j.healun.2011.10.003</identifier><identifier>PMID: 22153553</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Acute Disease ; acute rejection ; Animals ; Biological and medical sciences ; Cardiology. Vascular system ; dendritic cells ; Disease Models, Animal ; Disease Progression ; endothelium ; Endothelium - ultrastructure ; Follow-Up Studies ; Graft Rejection - pathology ; leukocytes ; Lung - ultrastructure ; Lung Transplantation - pathology ; Male ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Microscopy, Electron, Scanning ; mouse lung transplantation ; scanning electron microscopy ; Surgery ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the heart ; Transplantation, Homologous</subject><ispartof>The Journal of heart and lung transplantation, 2012, Vol.31 (1), p.94-100</ispartof><rights>International Society for Heart and Lung Transplantation</rights><rights>2012 International Society for Heart and Lung Transplantation</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. 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The assessment and classification of pathologic changes of AR relies essentially on conventional histology. Herein we apply the technique of scanning electron microscopy (SEM) to identify and characterize ultrastructural changes of the pulmonary graft after lung Tx. Methods Orthotopic single-lung Tx was performed between BALB/c (donor) and C57BL/6 (recipient) mice. At Day 5 after Tx, lung allografts were recovered for SEM and for histologic analysis. Results Upon Tx, high numbers of leukocytes and thrombocytes were found, showing an activated surface pattern and a change of their cell body shape. These cells adhered and partly transmigrated through the endothelium of vessels. Larger vessels were more affected than smaller vessels and the endothelium was roughened in its surface texture throughout. As a phenomenon, airways were partly covered by activated dendritic cells. Numerous thrombocytes and macrophages accumulated on the endothelium of the cuff anastomosis region exposing this area to a particularly higher risk of thrombosis. Conclusions SEM allows for detection of morphologic changes during pulmonary allograft rejection and adds important data to conventional histology when making the diagnosis of acute rejection.</description><subject>Acute Disease</subject><subject>acute rejection</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cardiology. Vascular system</subject><subject>dendritic cells</subject><subject>Disease Models, Animal</subject><subject>Disease Progression</subject><subject>endothelium</subject><subject>Endothelium - ultrastructure</subject><subject>Follow-Up Studies</subject><subject>Graft Rejection - pathology</subject><subject>leukocytes</subject><subject>Lung - ultrastructure</subject><subject>Lung Transplantation - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Microscopy, Electron, Scanning</subject><subject>mouse lung transplantation</subject><subject>scanning electron microscopy</subject><subject>Surgery</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. 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Vascular system</topic><topic>dendritic cells</topic><topic>Disease Models, Animal</topic><topic>Disease Progression</topic><topic>endothelium</topic><topic>Endothelium - ultrastructure</topic><topic>Follow-Up Studies</topic><topic>Graft Rejection - pathology</topic><topic>leukocytes</topic><topic>Lung - ultrastructure</topic><topic>Lung Transplantation - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Microscopy, Electron, Scanning</topic><topic>mouse lung transplantation</topic><topic>scanning electron microscopy</topic><topic>Surgery</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the heart</topic><topic>Transplantation, Homologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jungraithmayr, Wolfgang, MD</creatorcontrib><creatorcontrib>Draenert, Alice, MD</creatorcontrib><creatorcontrib>Marquardt, Klaus</creatorcontrib><creatorcontrib>Weder, Walter, MD</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of heart and lung transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jungraithmayr, Wolfgang, MD</au><au>Draenert, Alice, MD</au><au>Marquardt, Klaus</au><au>Weder, Walter, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ultrastructural changes in acute lung allograft rejection: Novel insights from an animal study</atitle><jtitle>The Journal of heart and lung transplantation</jtitle><addtitle>J Heart Lung Transplant</addtitle><date>2012</date><risdate>2012</risdate><volume>31</volume><issue>1</issue><spage>94</spage><epage>100</epage><pages>94-100</pages><issn>1053-2498</issn><eissn>1557-3117</eissn><abstract>Background Acute rejection (AR) episodes after lung transplantation (Tx) are orchestrated by cells of the innate and adaptive immune system targeting the engrafted organ. The assessment and classification of pathologic changes of AR relies essentially on conventional histology. Herein we apply the technique of scanning electron microscopy (SEM) to identify and characterize ultrastructural changes of the pulmonary graft after lung Tx. Methods Orthotopic single-lung Tx was performed between BALB/c (donor) and C57BL/6 (recipient) mice. At Day 5 after Tx, lung allografts were recovered for SEM and for histologic analysis. Results Upon Tx, high numbers of leukocytes and thrombocytes were found, showing an activated surface pattern and a change of their cell body shape. These cells adhered and partly transmigrated through the endothelium of vessels. Larger vessels were more affected than smaller vessels and the endothelium was roughened in its surface texture throughout. As a phenomenon, airways were partly covered by activated dendritic cells. Numerous thrombocytes and macrophages accumulated on the endothelium of the cuff anastomosis region exposing this area to a particularly higher risk of thrombosis. Conclusions SEM allows for detection of morphologic changes during pulmonary allograft rejection and adds important data to conventional histology when making the diagnosis of acute rejection.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>22153553</pmid><doi>10.1016/j.healun.2011.10.003</doi><tpages>7</tpages></addata></record>
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subjects Acute Disease
acute rejection
Animals
Biological and medical sciences
Cardiology. Vascular system
dendritic cells
Disease Models, Animal
Disease Progression
endothelium
Endothelium - ultrastructure
Follow-Up Studies
Graft Rejection - pathology
leukocytes
Lung - ultrastructure
Lung Transplantation - pathology
Male
Medical sciences
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Microscopy, Electron, Scanning
mouse lung transplantation
scanning electron microscopy
Surgery
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Surgery of the heart
Transplantation, Homologous
title Ultrastructural changes in acute lung allograft rejection: Novel insights from an animal study
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