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Application of Calculated Panel Reactive Antibody Using HLA Frequencies in Koreans
BACKGROUND: Introduction of the Luminex panel reactive antibody (PRA)-single antigen (SA) assay has increased the detection rates of unacceptable antigens in sensitized patients; the calculated PRA (CPRA) level represents the percentage of actual organ donors that express 1 or more of these unaccept...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Laboratory Medicine
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255493/ https://www.ncbi.nlm.nih.gov/pubmed/22259781 http://dx.doi.org/10.3343/alm.2012.32.1.66 |
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author | Jang, Ji-Young Kim, Yoon-Joo Kim, Yonggoo Park, Yeon-Joon Han, Kyungja Oh, Eun-Jee |
author_facet | Jang, Ji-Young Kim, Yoon-Joo Kim, Yonggoo Park, Yeon-Joon Han, Kyungja Oh, Eun-Jee |
author_sort | Jang, Ji-Young |
collection | PubMed |
description | BACKGROUND: Introduction of the Luminex panel reactive antibody (PRA)-single antigen (SA) assay has increased the detection rates of unacceptable antigens in sensitized patients; the calculated PRA (CPRA) level represents the percentage of actual organ donors that express 1 or more of these unacceptable antigens. We developed a CPRA calculator based on the HLA frequencies in Koreans to measure sensitization levels in Korean patients. METHODS: To develop the calculator, we obtained the HLA-A, HLA-B, and HLA-DR phenotypes of 1,622 Koreans, and compared these with previously reported frequencies in Koreans. Sera from patients awaiting kidney transplantation were tested for HLA antibodies by Luminex PRA-screen, PRA-identification (ID), and PRA-SA assays. The measured %PRA from the PRA-screen (N=55) and PRA-ID (N=71) were compared to the %CPRA for the unacceptable antigens obtained from PRA-SA. RESULTS: Phenotype frequencies used for the CPRA calculator agreed with previously reported data. The concordance rates among the 3 PRA methods for the detection of class I and class II antibodies were 76.1-81.8% (kappa, 0.519-0.636) and 72.7-83.6% (0.463-0.650), respectively. For the detection of broadly sensitized sera (>50% or >80%), the concordance rates were over 80%. In sera with 80-100% CPRA, 91.7% and 94.4% of the samples had concordant results (80-100% PRA) in the PRA-screen and PRA-ID assay, respectively. CONCLUSIONS: Although further clinical studies are required to confirm the benefits of CPRA values, adoption of CPRA analysis based on HLA frequencies in Koreans may be useful for sensitization measurements and organ-allocation algorithms. |
format | Online Article Text |
id | pubmed-3255493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Korean Society for Laboratory Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-32554932012-01-18 Application of Calculated Panel Reactive Antibody Using HLA Frequencies in Koreans Jang, Ji-Young Kim, Yoon-Joo Kim, Yonggoo Park, Yeon-Joon Han, Kyungja Oh, Eun-Jee Ann Lab Med Original Article BACKGROUND: Introduction of the Luminex panel reactive antibody (PRA)-single antigen (SA) assay has increased the detection rates of unacceptable antigens in sensitized patients; the calculated PRA (CPRA) level represents the percentage of actual organ donors that express 1 or more of these unacceptable antigens. We developed a CPRA calculator based on the HLA frequencies in Koreans to measure sensitization levels in Korean patients. METHODS: To develop the calculator, we obtained the HLA-A, HLA-B, and HLA-DR phenotypes of 1,622 Koreans, and compared these with previously reported frequencies in Koreans. Sera from patients awaiting kidney transplantation were tested for HLA antibodies by Luminex PRA-screen, PRA-identification (ID), and PRA-SA assays. The measured %PRA from the PRA-screen (N=55) and PRA-ID (N=71) were compared to the %CPRA for the unacceptable antigens obtained from PRA-SA. RESULTS: Phenotype frequencies used for the CPRA calculator agreed with previously reported data. The concordance rates among the 3 PRA methods for the detection of class I and class II antibodies were 76.1-81.8% (kappa, 0.519-0.636) and 72.7-83.6% (0.463-0.650), respectively. For the detection of broadly sensitized sera (>50% or >80%), the concordance rates were over 80%. In sera with 80-100% CPRA, 91.7% and 94.4% of the samples had concordant results (80-100% PRA) in the PRA-screen and PRA-ID assay, respectively. CONCLUSIONS: Although further clinical studies are required to confirm the benefits of CPRA values, adoption of CPRA analysis based on HLA frequencies in Koreans may be useful for sensitization measurements and organ-allocation algorithms. The Korean Society for Laboratory Medicine 2012-01 2011-12-20 /pmc/articles/PMC3255493/ /pubmed/22259781 http://dx.doi.org/10.3343/alm.2012.32.1.66 Text en © The Korean Society for Laboratory Medicine http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Jang, Ji-Young Kim, Yoon-Joo Kim, Yonggoo Park, Yeon-Joon Han, Kyungja Oh, Eun-Jee Application of Calculated Panel Reactive Antibody Using HLA Frequencies in Koreans |
title | Application of Calculated Panel Reactive Antibody Using HLA Frequencies in Koreans |
title_full | Application of Calculated Panel Reactive Antibody Using HLA Frequencies in Koreans |
title_fullStr | Application of Calculated Panel Reactive Antibody Using HLA Frequencies in Koreans |
title_full_unstemmed | Application of Calculated Panel Reactive Antibody Using HLA Frequencies in Koreans |
title_short | Application of Calculated Panel Reactive Antibody Using HLA Frequencies in Koreans |
title_sort | application of calculated panel reactive antibody using hla frequencies in koreans |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255493/ https://www.ncbi.nlm.nih.gov/pubmed/22259781 http://dx.doi.org/10.3343/alm.2012.32.1.66 |
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