C4d staining of renal allograft biopsies: a comparative analysis of different staining techniques
Background. Detection of C4d along peritubular capillaries (PTC) in renal allograft biopsies is an independent prognostic marker of poor long-term graft survival. It is typically associated with circulating donor-specific antibodies. Since only little information is available on the best technique t...
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description | Background. Detection of C4d along peritubular capillaries (PTC) in renal allograft biopsies is an independent prognostic marker of poor long-term graft survival. It is typically associated with circulating donor-specific antibodies. Since only little information is available on the best technique to stain C4d, we compared the two methods most often used for detecting C4d in renal allograft specimens. Methods. We investigated the expression of C4d along PTC in 64 renal allograft biopsies using a monoclonal antibody (Quidel) and immunofluorescence for frozen (F-IF) and a polyclonal antibody (Biomedica) and immunohistochemistry for formalin-fixed and paraffin-embedded (P-IHC) tissue samples. We compared the staining extent (diffuse, focal, minimal, no staining) in frozen and paraffin sections and evaluated the intra- and inter-observer concordance rates using kappa statistics. In addition, we determined the inter-observer concordance in 240 paraffin-embedded biopsies of a multi-centre study. Results. The inter- and intra-investigator concordance rate (κ = 0.9) of analysing the C4d expression by F-IF was excellent. In contrast, the detection of C4d by P-IHC demonstrated a substantially lower prevalence and extent of C4d expression with a lower intra- and inter-observer concordance rate (κ = 0.3). Only 69% of diffuse and 13% of focal C4d-expressing cases were in line classified by F-IF and P-IHC. On average, the estimated area of C4d-positive PTC in the diffuse group was 36% lower by P-IHC than by F-IF. The inter-observer concordance rate in paraffin of the 64 renal biopsies and the multi-centre study was good, but not perfect (κ = 0.57 or 0.67). Conclusions. C4d staining determined on frozen tissue samples using F-IF with a monoclonal antibody appears to be better suited for diagnostic as well as research purposes. Future studies should correlate C4d staining patterns with circulating donor-specific antibodies. |
doi_str_mv | 10.1093/ndt/gfl594 |
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Detection of C4d along peritubular capillaries (PTC) in renal allograft biopsies is an independent prognostic marker of poor long-term graft survival. It is typically associated with circulating donor-specific antibodies. Since only little information is available on the best technique to stain C4d, we compared the two methods most often used for detecting C4d in renal allograft specimens. Methods. We investigated the expression of C4d along PTC in 64 renal allograft biopsies using a monoclonal antibody (Quidel) and immunofluorescence for frozen (F-IF) and a polyclonal antibody (Biomedica) and immunohistochemistry for formalin-fixed and paraffin-embedded (P-IHC) tissue samples. We compared the staining extent (diffuse, focal, minimal, no staining) in frozen and paraffin sections and evaluated the intra- and inter-observer concordance rates using kappa statistics. In addition, we determined the inter-observer concordance in 240 paraffin-embedded biopsies of a multi-centre study. Results. The inter- and intra-investigator concordance rate (κ = 0.9) of analysing the C4d expression by F-IF was excellent. In contrast, the detection of C4d by P-IHC demonstrated a substantially lower prevalence and extent of C4d expression with a lower intra- and inter-observer concordance rate (κ = 0.3). Only 69% of diffuse and 13% of focal C4d-expressing cases were in line classified by F-IF and P-IHC. On average, the estimated area of C4d-positive PTC in the diffuse group was 36% lower by P-IHC than by F-IF. The inter-observer concordance rate in paraffin of the 64 renal biopsies and the multi-centre study was good, but not perfect (κ = 0.57 or 0.67). Conclusions. C4d staining determined on frozen tissue samples using F-IF with a monoclonal antibody appears to be better suited for diagnostic as well as research purposes. Future studies should correlate C4d staining patterns with circulating donor-specific antibodies.</description><identifier>ISSN: 0931-0509</identifier><identifier>EISSN: 1460-2385</identifier><identifier>DOI: 10.1093/ndt/gfl594</identifier><identifier>PMID: 17164320</identifier><identifier>CODEN: NDTREA</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Biopsy, Needle ; comparison of frozen vs paraffin sections ; Complement C4b - metabolism ; Emergency and intensive care: renal failure. Dialysis management ; Fluorescent Antibody Technique, Indirect ; Follow-Up Studies ; Graft Survival ; Humans ; humoral rejection ; Immunohistochemistry ; Intensive care medicine ; Kidney - metabolism ; Kidney - pathology ; Kidney Transplantation - pathology ; Medical sciences ; method of detection for C4d ; Nephrology. Urinary tract diseases ; Nephropathies. Renovascular diseases. Renal failure ; Observer Variation ; Peptide Fragments - metabolism ; Prognosis ; Renal failure ; renal transplantation ; Staining and Labeling - methods ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the urinary system ; Transplantation, Homologous</subject><ispartof>Nephrology, dialysis, transplantation, 2007-02, Vol.22 (2), p.568-576</ispartof><rights>The Author [2006]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2007</rights><rights>2007 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) Feb 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c543t-1005a29155e4b10eb4d4aefe55e504dfdad8682e4b1c05f95337704ef2d7a8453</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,1585,27929,27930</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18506262$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17164320$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Seemayer, Christian A.</creatorcontrib><creatorcontrib>Gaspert, Ariana</creatorcontrib><creatorcontrib>Nickeleit, Volker</creatorcontrib><creatorcontrib>Mihatsch, Michael J.</creatorcontrib><title>C4d staining of renal allograft biopsies: a comparative analysis of different staining techniques</title><title>Nephrology, dialysis, transplantation</title><addtitle>Nephrol Dial Transplant</addtitle><description>Background. Detection of C4d along peritubular capillaries (PTC) in renal allograft biopsies is an independent prognostic marker of poor long-term graft survival. It is typically associated with circulating donor-specific antibodies. Since only little information is available on the best technique to stain C4d, we compared the two methods most often used for detecting C4d in renal allograft specimens. Methods. We investigated the expression of C4d along PTC in 64 renal allograft biopsies using a monoclonal antibody (Quidel) and immunofluorescence for frozen (F-IF) and a polyclonal antibody (Biomedica) and immunohistochemistry for formalin-fixed and paraffin-embedded (P-IHC) tissue samples. We compared the staining extent (diffuse, focal, minimal, no staining) in frozen and paraffin sections and evaluated the intra- and inter-observer concordance rates using kappa statistics. In addition, we determined the inter-observer concordance in 240 paraffin-embedded biopsies of a multi-centre study. Results. The inter- and intra-investigator concordance rate (κ = 0.9) of analysing the C4d expression by F-IF was excellent. In contrast, the detection of C4d by P-IHC demonstrated a substantially lower prevalence and extent of C4d expression with a lower intra- and inter-observer concordance rate (κ = 0.3). Only 69% of diffuse and 13% of focal C4d-expressing cases were in line classified by F-IF and P-IHC. On average, the estimated area of C4d-positive PTC in the diffuse group was 36% lower by P-IHC than by F-IF. The inter-observer concordance rate in paraffin of the 64 renal biopsies and the multi-centre study was good, but not perfect (κ = 0.57 or 0.67). Conclusions. C4d staining determined on frozen tissue samples using F-IF with a monoclonal antibody appears to be better suited for diagnostic as well as research purposes. Future studies should correlate C4d staining patterns with circulating donor-specific antibodies.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Biopsy, Needle</subject><subject>comparison of frozen vs paraffin sections</subject><subject>Complement C4b - metabolism</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Follow-Up Studies</subject><subject>Graft Survival</subject><subject>Humans</subject><subject>humoral rejection</subject><subject>Immunohistochemistry</subject><subject>Intensive care medicine</subject><subject>Kidney - metabolism</subject><subject>Kidney - pathology</subject><subject>Kidney Transplantation - pathology</subject><subject>Medical sciences</subject><subject>method of detection for C4d</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nephropathies. Renovascular diseases. Renal failure</subject><subject>Observer Variation</subject><subject>Peptide Fragments - metabolism</subject><subject>Prognosis</subject><subject>Renal failure</subject><subject>renal transplantation</subject><subject>Staining and Labeling - methods</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the urinary system</subject><subject>Transplantation, Homologous</subject><issn>0931-0509</issn><issn>1460-2385</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0c-LEzEUB_AgilurF_8AGQQ9COO-_JyZvWlRqxS8rCJewuskqVmnkzHJiPvfm9JiwYOeQsjnvUfel5DHFF5S6PjlaPLlzg2yE3fIggoFNeOtvEsW5ZHWIKG7IA9SugGAjjXNfXJBG6oEZ7AguBKmShn96MddFVwV7YhDhcMQdhFdrrY-TMnbdFVh1Yf9hBGz_2krLOw2-XSoMd45WwrzuVO2_bfR_5htekjuORySfXQ6l-TT2zfXq3W9-fju_erVpu6l4LmmABJZR6W0YkvBboURaJ0tdwnCOIOmVS07PPYgXSc5bxoQ1jHTYCskX5Lnx75TDIe5We996u0w4GjDnLRqyzY6qf4LC5LQdlDg07_gTZhj-XfSjLZUcVaWuCQvjqiPIaVonZ6i32O81RT0IR5d4tHHeAp-cuo4b_fWnOkpjwKenQCmHgcXcex9OrtWgmKKnV2Yp38PrI_Op2x__ZEYv2vV8Ebq9Zev-lpuxObz-oN-zX8DFx20dw</recordid><startdate>20070201</startdate><enddate>20070201</enddate><creator>Seemayer, Christian A.</creator><creator>Gaspert, Ariana</creator><creator>Nickeleit, Volker</creator><creator>Mihatsch, Michael J.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20070201</creationdate><title>C4d staining of renal allograft biopsies: a comparative analysis of different staining techniques</title><author>Seemayer, Christian A. ; Gaspert, Ariana ; Nickeleit, Volker ; Mihatsch, Michael J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c543t-1005a29155e4b10eb4d4aefe55e504dfdad8682e4b1c05f95337704ef2d7a8453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Biopsy, Needle</topic><topic>comparison of frozen vs paraffin sections</topic><topic>Complement C4b - metabolism</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>Fluorescent Antibody Technique, Indirect</topic><topic>Follow-Up Studies</topic><topic>Graft Survival</topic><topic>Humans</topic><topic>humoral rejection</topic><topic>Immunohistochemistry</topic><topic>Intensive care medicine</topic><topic>Kidney - metabolism</topic><topic>Kidney - pathology</topic><topic>Kidney Transplantation - pathology</topic><topic>Medical sciences</topic><topic>method of detection for C4d</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Nephropathies. Renovascular diseases. Renal failure</topic><topic>Observer Variation</topic><topic>Peptide Fragments - metabolism</topic><topic>Prognosis</topic><topic>Renal failure</topic><topic>renal transplantation</topic><topic>Staining and Labeling - methods</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the urinary system</topic><topic>Transplantation, Homologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seemayer, Christian A.</creatorcontrib><creatorcontrib>Gaspert, Ariana</creatorcontrib><creatorcontrib>Nickeleit, Volker</creatorcontrib><creatorcontrib>Mihatsch, Michael J.</creatorcontrib><collection>Istex</collection><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>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Nephrology, dialysis, transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seemayer, Christian A.</au><au>Gaspert, Ariana</au><au>Nickeleit, Volker</au><au>Mihatsch, Michael J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>C4d staining of renal allograft biopsies: a comparative analysis of different staining techniques</atitle><jtitle>Nephrology, dialysis, transplantation</jtitle><addtitle>Nephrol Dial Transplant</addtitle><date>2007-02-01</date><risdate>2007</risdate><volume>22</volume><issue>2</issue><spage>568</spage><epage>576</epage><pages>568-576</pages><issn>0931-0509</issn><eissn>1460-2385</eissn><coden>NDTREA</coden><abstract>Background. Detection of C4d along peritubular capillaries (PTC) in renal allograft biopsies is an independent prognostic marker of poor long-term graft survival. It is typically associated with circulating donor-specific antibodies. Since only little information is available on the best technique to stain C4d, we compared the two methods most often used for detecting C4d in renal allograft specimens. Methods. We investigated the expression of C4d along PTC in 64 renal allograft biopsies using a monoclonal antibody (Quidel) and immunofluorescence for frozen (F-IF) and a polyclonal antibody (Biomedica) and immunohistochemistry for formalin-fixed and paraffin-embedded (P-IHC) tissue samples. We compared the staining extent (diffuse, focal, minimal, no staining) in frozen and paraffin sections and evaluated the intra- and inter-observer concordance rates using kappa statistics. In addition, we determined the inter-observer concordance in 240 paraffin-embedded biopsies of a multi-centre study. Results. The inter- and intra-investigator concordance rate (κ = 0.9) of analysing the C4d expression by F-IF was excellent. In contrast, the detection of C4d by P-IHC demonstrated a substantially lower prevalence and extent of C4d expression with a lower intra- and inter-observer concordance rate (κ = 0.3). Only 69% of diffuse and 13% of focal C4d-expressing cases were in line classified by F-IF and P-IHC. On average, the estimated area of C4d-positive PTC in the diffuse group was 36% lower by P-IHC than by F-IF. The inter-observer concordance rate in paraffin of the 64 renal biopsies and the multi-centre study was good, but not perfect (κ = 0.57 or 0.67). Conclusions. C4d staining determined on frozen tissue samples using F-IF with a monoclonal antibody appears to be better suited for diagnostic as well as research purposes. Future studies should correlate C4d staining patterns with circulating donor-specific antibodies.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>17164320</pmid><doi>10.1093/ndt/gfl594</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Biopsy, Needle comparison of frozen vs paraffin sections Complement C4b - metabolism Emergency and intensive care: renal failure. Dialysis management Fluorescent Antibody Technique, Indirect Follow-Up Studies Graft Survival Humans humoral rejection Immunohistochemistry Intensive care medicine Kidney - metabolism Kidney - pathology Kidney Transplantation - pathology Medical sciences method of detection for C4d Nephrology. Urinary tract diseases Nephropathies. Renovascular diseases. Renal failure Observer Variation Peptide Fragments - metabolism Prognosis Renal failure renal transplantation Staining and Labeling - methods Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the urinary system Transplantation, Homologous |
title | C4d staining of renal allograft biopsies: a comparative analysis of different staining techniques |
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