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Clinical relevance of donor-specific human leukocyte antigen antibodies after pediatric liver transplantation

Donor-specific human leukocyte antigen (HLA) antibodies (DSAs) have a significant role in graft survival after pediatric liver transplantation. To understand the significance of DSAs, a retrospective cohort study of 48 pediatric liver transplant recipients with posttransplant serum samples that were...

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Autores principales: Liu, Wei, Wang, Kai, Xiao, Yan-Li, Liu, Chun, Gao, Wei, Li, Dai-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237393/
https://www.ncbi.nlm.nih.gov/pubmed/34194545
http://dx.doi.org/10.3892/etm.2021.10299
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author Liu, Wei
Wang, Kai
Xiao, Yan-Li
Liu, Chun
Gao, Wei
Li, Dai-Hong
author_facet Liu, Wei
Wang, Kai
Xiao, Yan-Li
Liu, Chun
Gao, Wei
Li, Dai-Hong
author_sort Liu, Wei
collection PubMed
description Donor-specific human leukocyte antigen (HLA) antibodies (DSAs) have a significant role in graft survival after pediatric liver transplantation. To understand the significance of DSAs, a retrospective cohort study of 48 pediatric liver transplant recipients with posttransplant serum samples that were analyzed for DSAs was performed. According to their test results, the recipients were divided into a DSA-positive group and a DSA-negative group. Postoperative liver transplantation biopsies were performed in patients with abnormal liver function. The liver condition and prognosis of the recipients were recorded, and their association was analyzed. A total of 48 recipients were followed up for 2.7±0.8 years. DSA positivity was detected in 10 cases (20.8%). One case was positive for HLA class I and HLA class II antibodies, whereas 9 cases were positive for HLA class II antibodies, and the gene loci were HLA-DR and/or DQ. Antibody-mediated rejection (AMR) occurred in four of 10 patients in the DSA-positive group. Liver function was abnormal in 3 of 38 cases in the DSA-negative group. Multivariate analysis revealed that DSA positivity was an independent risk factor for liver insufficiency and long-term survival of recipients. In addition, Kaplan-Meier survival analysis demonstrated that there were significant differences in the survival of graft recipients between the DSA-positive group and the DSA-negative group (P<0.05). The positivity of DSAs after pediatric liver transplantation was closely related to the occurrence of AMR. These results suggested that DSAs should be routinely monitored post-operatively, and that DSA-positive recipients should be screened as soon as possible and given appropriate treatment.
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spelling pubmed-82373932021-06-29 Clinical relevance of donor-specific human leukocyte antigen antibodies after pediatric liver transplantation Liu, Wei Wang, Kai Xiao, Yan-Li Liu, Chun Gao, Wei Li, Dai-Hong Exp Ther Med Articles Donor-specific human leukocyte antigen (HLA) antibodies (DSAs) have a significant role in graft survival after pediatric liver transplantation. To understand the significance of DSAs, a retrospective cohort study of 48 pediatric liver transplant recipients with posttransplant serum samples that were analyzed for DSAs was performed. According to their test results, the recipients were divided into a DSA-positive group and a DSA-negative group. Postoperative liver transplantation biopsies were performed in patients with abnormal liver function. The liver condition and prognosis of the recipients were recorded, and their association was analyzed. A total of 48 recipients were followed up for 2.7±0.8 years. DSA positivity was detected in 10 cases (20.8%). One case was positive for HLA class I and HLA class II antibodies, whereas 9 cases were positive for HLA class II antibodies, and the gene loci were HLA-DR and/or DQ. Antibody-mediated rejection (AMR) occurred in four of 10 patients in the DSA-positive group. Liver function was abnormal in 3 of 38 cases in the DSA-negative group. Multivariate analysis revealed that DSA positivity was an independent risk factor for liver insufficiency and long-term survival of recipients. In addition, Kaplan-Meier survival analysis demonstrated that there were significant differences in the survival of graft recipients between the DSA-positive group and the DSA-negative group (P<0.05). The positivity of DSAs after pediatric liver transplantation was closely related to the occurrence of AMR. These results suggested that DSAs should be routinely monitored post-operatively, and that DSA-positive recipients should be screened as soon as possible and given appropriate treatment. D.A. Spandidos 2021-08 2021-06-13 /pmc/articles/PMC8237393/ /pubmed/34194545 http://dx.doi.org/10.3892/etm.2021.10299 Text en Copyright: © Liu et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Liu, Wei
Wang, Kai
Xiao, Yan-Li
Liu, Chun
Gao, Wei
Li, Dai-Hong
Clinical relevance of donor-specific human leukocyte antigen antibodies after pediatric liver transplantation
title Clinical relevance of donor-specific human leukocyte antigen antibodies after pediatric liver transplantation
title_full Clinical relevance of donor-specific human leukocyte antigen antibodies after pediatric liver transplantation
title_fullStr Clinical relevance of donor-specific human leukocyte antigen antibodies after pediatric liver transplantation
title_full_unstemmed Clinical relevance of donor-specific human leukocyte antigen antibodies after pediatric liver transplantation
title_short Clinical relevance of donor-specific human leukocyte antigen antibodies after pediatric liver transplantation
title_sort clinical relevance of donor-specific human leukocyte antigen antibodies after pediatric liver transplantation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237393/
https://www.ncbi.nlm.nih.gov/pubmed/34194545
http://dx.doi.org/10.3892/etm.2021.10299
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