Expression of cytotoxic mediators (perforin, granzyme B, FAS, and FAS-l) in renal allograft biopsies

Objectives: To analyze the in situ expression of perforin, granzymeB, FAS-L and FAS in renal allograft biopsies by means ofimmunohistochemistry and correlate these findings with the degreeof histologic rejection and allograft outcome. Methods: Ninety-sixallograft biopsies were divided into three gro...

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Main Authors: Therezinha Gauri Leitão, Luís Eduardo Becker, Ivone Braga de Oliveira, Flávia Ramos de Siqueira, Maria Regina Teixeira Araújo, João Egídio Romão Junior, Hugo Abensur, Irene de Lourdes Noronha
Format: Article
Language:English
Published: Instituto Israelita de Ensino e Pesquisa Albert Einstein 2006-12-01
Series:Einstein (São Paulo)
Subjects:
Online Access:http://www.einstein.br/revista/arquivos/PDF/Einstein_vol4_n4_2006_p277.pdf
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author Therezinha Gauri Leitão
Luís Eduardo Becker
Ivone Braga de Oliveira
Flávia Ramos de Siqueira
Maria Regina Teixeira Araújo
João Egídio Romão Junior
Hugo Abensur
Irene de Lourdes Noronha
author_facet Therezinha Gauri Leitão
Luís Eduardo Becker
Ivone Braga de Oliveira
Flávia Ramos de Siqueira
Maria Regina Teixeira Araújo
João Egídio Romão Junior
Hugo Abensur
Irene de Lourdes Noronha
author_sort Therezinha Gauri Leitão
collection DOAJ
description Objectives: To analyze the in situ expression of perforin, granzymeB, FAS-L and FAS in renal allograft biopsies by means ofimmunohistochemistry and correlate these findings with the degreeof histologic rejection and allograft outcome. Methods: Ninety-sixallograft biopsies were divided into three groups: acute rejection (n= 56), chronic rejection (n = 31), and cases with stable renal function(no rejection; n = 9). The expression of perforin, granzyme B, FAS-L,and FAS was evaluated by immunohistochemistry. Results: Asignificantly higher expression of perforin and granzyme B wasobserved in acute rejection biopsies (4.83 ± 0.65 and 30.05 ± 7.93cells/mm2) compared to chronic rejection biopsies (0.71 ± 0.13 and11.4 ± 3.84 cells/mm2; p < 0.001, and p <0.05, respectively), but thiswas not the case for FAS-L (24.44 ± 5.56 in acute rejection versus 18.87± 6.83 in chronic rejection). Perforin, granzyme B, and FAS-L expressionwas significantly higher in the acute rejection group compared to the norejection and control groups. FAS expression was similar in all groups. Amodest correlation between perforin expression and the severity of ARwas observed (r = 0.28, p = 0.05). Perforin was the most reliable markerfor acute rejection diagnosis, with 80% sensitivity and 84.3% specificity.Conclusion: The in situ expression of perforin, granzyme B, and FAS-Lin AR reflects the presence of an active cytotoxic process. Additionalallograft biopsies are necessary in order to evaluate the usefulness ofthese markers for allograft rejection monitoring.
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spelling doaj.art-b91fd6496c894b0880ca954e94ce20472022-12-22T02:29:11ZengInstituto Israelita de Ensino e Pesquisa Albert EinsteinEinstein (São Paulo)1679-45082006-12-0144277283Expression of cytotoxic mediators (perforin, granzyme B, FAS, and FAS-l) in renal allograft biopsiesTherezinha Gauri LeitãoLuís Eduardo BeckerIvone Braga de OliveiraFlávia Ramos de SiqueiraMaria Regina Teixeira AraújoJoão Egídio Romão JuniorHugo AbensurIrene de Lourdes NoronhaObjectives: To analyze the in situ expression of perforin, granzymeB, FAS-L and FAS in renal allograft biopsies by means ofimmunohistochemistry and correlate these findings with the degreeof histologic rejection and allograft outcome. Methods: Ninety-sixallograft biopsies were divided into three groups: acute rejection (n= 56), chronic rejection (n = 31), and cases with stable renal function(no rejection; n = 9). The expression of perforin, granzyme B, FAS-L,and FAS was evaluated by immunohistochemistry. Results: Asignificantly higher expression of perforin and granzyme B wasobserved in acute rejection biopsies (4.83 ± 0.65 and 30.05 ± 7.93cells/mm2) compared to chronic rejection biopsies (0.71 ± 0.13 and11.4 ± 3.84 cells/mm2; p < 0.001, and p <0.05, respectively), but thiswas not the case for FAS-L (24.44 ± 5.56 in acute rejection versus 18.87± 6.83 in chronic rejection). Perforin, granzyme B, and FAS-L expressionwas significantly higher in the acute rejection group compared to the norejection and control groups. FAS expression was similar in all groups. Amodest correlation between perforin expression and the severity of ARwas observed (r = 0.28, p = 0.05). Perforin was the most reliable markerfor acute rejection diagnosis, with 80% sensitivity and 84.3% specificity.Conclusion: The in situ expression of perforin, granzyme B, and FAS-Lin AR reflects the presence of an active cytotoxic process. Additionalallograft biopsies are necessary in order to evaluate the usefulness ofthese markers for allograft rejection monitoring.http://www.einstein.br/revista/arquivos/PDF/Einstein_vol4_n4_2006_p277.pdfKidney transplantation/immunologyKidney/pathologyImmunohistochemistryAntigensCD95Graft rejection
spellingShingle Therezinha Gauri Leitão
Luís Eduardo Becker
Ivone Braga de Oliveira
Flávia Ramos de Siqueira
Maria Regina Teixeira Araújo
João Egídio Romão Junior
Hugo Abensur
Irene de Lourdes Noronha
Expression of cytotoxic mediators (perforin, granzyme B, FAS, and FAS-l) in renal allograft biopsies
Einstein (São Paulo)
Kidney transplantation/immunology
Kidney/pathology
Immunohistochemistry
Antigens
CD95
Graft rejection
title Expression of cytotoxic mediators (perforin, granzyme B, FAS, and FAS-l) in renal allograft biopsies
title_full Expression of cytotoxic mediators (perforin, granzyme B, FAS, and FAS-l) in renal allograft biopsies
title_fullStr Expression of cytotoxic mediators (perforin, granzyme B, FAS, and FAS-l) in renal allograft biopsies
title_full_unstemmed Expression of cytotoxic mediators (perforin, granzyme B, FAS, and FAS-l) in renal allograft biopsies
title_short Expression of cytotoxic mediators (perforin, granzyme B, FAS, and FAS-l) in renal allograft biopsies
title_sort expression of cytotoxic mediators perforin granzyme b fas and fas l in renal allograft biopsies
topic Kidney transplantation/immunology
Kidney/pathology
Immunohistochemistry
Antigens
CD95
Graft rejection
url http://www.einstein.br/revista/arquivos/PDF/Einstein_vol4_n4_2006_p277.pdf
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