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Impact of Antibodies That React With Liver Tissue and Donor-Specific Anti-HLA Antibodies in Pediatric Idiopathic Posttransplantation Hepatitis

BACKGROUND: The cause of late graft dysfunction has not been elucidated. Although an antibody-mediated reaction is suspected as a potential mechanism, the target antigens have not been clarified. METHODS: To clarify the etiology of idiopathic posttransplantation hepatitis (IPTH), we simultaneously e...

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Autores principales: Hirata, Yoshihiro, Yoshizawa, Atsushi, Egawa, Hiroto, Ueda, Daisuke, Okamoto, Shinya, Okajima, Hideaki, Yurugi, Kimiko, Hishida, Rie, Hirai, Hideyo, Miyagawa-Hayashino, Aya, Maekawa, Taira, Haga, Hironori, Uemoto, Sinji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642348/
https://www.ncbi.nlm.nih.gov/pubmed/28118175
http://dx.doi.org/10.1097/TP.0000000000001653
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author Hirata, Yoshihiro
Yoshizawa, Atsushi
Egawa, Hiroto
Ueda, Daisuke
Okamoto, Shinya
Okajima, Hideaki
Yurugi, Kimiko
Hishida, Rie
Hirai, Hideyo
Miyagawa-Hayashino, Aya
Maekawa, Taira
Haga, Hironori
Uemoto, Sinji
author_facet Hirata, Yoshihiro
Yoshizawa, Atsushi
Egawa, Hiroto
Ueda, Daisuke
Okamoto, Shinya
Okajima, Hideaki
Yurugi, Kimiko
Hishida, Rie
Hirai, Hideyo
Miyagawa-Hayashino, Aya
Maekawa, Taira
Haga, Hironori
Uemoto, Sinji
author_sort Hirata, Yoshihiro
collection PubMed
description BACKGROUND: The cause of late graft dysfunction has not been elucidated. Although an antibody-mediated reaction is suspected as a potential mechanism, the target antigens have not been clarified. METHODS: To clarify the etiology of idiopathic posttransplantation hepatitis (IPTH), we simultaneously examined the presence of antibodies that react with liver tissue (ARLT) by means of indirect immunofluorescence staining, as well as the presence of donor-specific anti-human leukocyte antigen antibodies (HLA-DSA). A subanalysis of the IPTH group was also performed. Within the IPTH group, the correlation between ARLT titer and clinical data were analyzed. RESULTS: In the sera of patients with IPTH (30 patients), ARLT were found at a significantly higher frequency than in patients without IPTH (42 patients; P < 0.001). Moreover, the ARLT titer appeared to be correlated with the severity of hepatitis or hepatic injury. In contrast, the frequency of HLA-DSA was significantly lower in patients with IPTH than in patients without IPTH (P = 0.001). CONCLUSION: Our findings indicate that ARLT, and not HLA-DSA, profoundly influence the etiology of IPTH.
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spelling pubmed-56423482017-10-24 Impact of Antibodies That React With Liver Tissue and Donor-Specific Anti-HLA Antibodies in Pediatric Idiopathic Posttransplantation Hepatitis Hirata, Yoshihiro Yoshizawa, Atsushi Egawa, Hiroto Ueda, Daisuke Okamoto, Shinya Okajima, Hideaki Yurugi, Kimiko Hishida, Rie Hirai, Hideyo Miyagawa-Hayashino, Aya Maekawa, Taira Haga, Hironori Uemoto, Sinji Transplantation Original Clinical Science—Liver BACKGROUND: The cause of late graft dysfunction has not been elucidated. Although an antibody-mediated reaction is suspected as a potential mechanism, the target antigens have not been clarified. METHODS: To clarify the etiology of idiopathic posttransplantation hepatitis (IPTH), we simultaneously examined the presence of antibodies that react with liver tissue (ARLT) by means of indirect immunofluorescence staining, as well as the presence of donor-specific anti-human leukocyte antigen antibodies (HLA-DSA). A subanalysis of the IPTH group was also performed. Within the IPTH group, the correlation between ARLT titer and clinical data were analyzed. RESULTS: In the sera of patients with IPTH (30 patients), ARLT were found at a significantly higher frequency than in patients without IPTH (42 patients; P < 0.001). Moreover, the ARLT titer appeared to be correlated with the severity of hepatitis or hepatic injury. In contrast, the frequency of HLA-DSA was significantly lower in patients with IPTH than in patients without IPTH (P = 0.001). CONCLUSION: Our findings indicate that ARLT, and not HLA-DSA, profoundly influence the etiology of IPTH. Lippincott Williams & Wilkins 2017-05 2017-01-21 /pmc/articles/PMC5642348/ /pubmed/28118175 http://dx.doi.org/10.1097/TP.0000000000001653 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 Original Clinical Science—Liver
Hirata, Yoshihiro
Yoshizawa, Atsushi
Egawa, Hiroto
Ueda, Daisuke
Okamoto, Shinya
Okajima, Hideaki
Yurugi, Kimiko
Hishida, Rie
Hirai, Hideyo
Miyagawa-Hayashino, Aya
Maekawa, Taira
Haga, Hironori
Uemoto, Sinji
Impact of Antibodies That React With Liver Tissue and Donor-Specific Anti-HLA Antibodies in Pediatric Idiopathic Posttransplantation Hepatitis
title Impact of Antibodies That React With Liver Tissue and Donor-Specific Anti-HLA Antibodies in Pediatric Idiopathic Posttransplantation Hepatitis
title_full Impact of Antibodies That React With Liver Tissue and Donor-Specific Anti-HLA Antibodies in Pediatric Idiopathic Posttransplantation Hepatitis
title_fullStr Impact of Antibodies That React With Liver Tissue and Donor-Specific Anti-HLA Antibodies in Pediatric Idiopathic Posttransplantation Hepatitis
title_full_unstemmed Impact of Antibodies That React With Liver Tissue and Donor-Specific Anti-HLA Antibodies in Pediatric Idiopathic Posttransplantation Hepatitis
title_short Impact of Antibodies That React With Liver Tissue and Donor-Specific Anti-HLA Antibodies in Pediatric Idiopathic Posttransplantation Hepatitis
title_sort impact of antibodies that react with liver tissue and donor-specific anti-hla antibodies in pediatric idiopathic posttransplantation hepatitis
topic Original Clinical Science—Liver
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642348/
https://www.ncbi.nlm.nih.gov/pubmed/28118175
http://dx.doi.org/10.1097/TP.0000000000001653
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