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Non-Inherited Maternal Antigens Identify Acceptable HLA Mismatches: A New Policy for the Hellenic Cord Blood Bank

Background: During pregnancy, the maternal-fetal contact may lead to the development of tolerance against the maternal human leukocyte antigen (HLA) that is not inherited by the fetus. These non-inherited maternal antigens (NIMAs) define acceptable HLA mismatches; therefore, the number of HLA phenot...

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Autores principales: Panagouli, Effrosyni, Dinou, Amalia, Mallis, Panagiotis, Michalopoulos, Efstathios, Papassavas, Andreas, Spyropoulou-Vlachou, Maria, Meletis, John, Angelopoulou, Maria, Konstantopoulos, Kostas, Vassilakopoulos, Theodoros, Stavropoulos-Giokas, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316301/
https://www.ncbi.nlm.nih.gov/pubmed/30248919
http://dx.doi.org/10.3390/bioengineering5040077
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author Panagouli, Effrosyni
Dinou, Amalia
Mallis, Panagiotis
Michalopoulos, Efstathios
Papassavas, Andreas
Spyropoulou-Vlachou, Maria
Meletis, John
Angelopoulou, Maria
Konstantopoulos, Kostas
Vassilakopoulos, Theodoros
Stavropoulos-Giokas, Catherine
author_facet Panagouli, Effrosyni
Dinou, Amalia
Mallis, Panagiotis
Michalopoulos, Efstathios
Papassavas, Andreas
Spyropoulou-Vlachou, Maria
Meletis, John
Angelopoulou, Maria
Konstantopoulos, Kostas
Vassilakopoulos, Theodoros
Stavropoulos-Giokas, Catherine
author_sort Panagouli, Effrosyni
collection PubMed
description Background: During pregnancy, the maternal-fetal contact may lead to the development of tolerance against the maternal human leukocyte antigen (HLA) that is not inherited by the fetus. These non-inherited maternal antigens (NIMAs) define acceptable HLA mismatches; therefore, the number of HLA phenotypes that are suitable matches for patients who need a hematopoietic stem cell transplant could be increased. Cord blood unit (CBU) transplantations to patients mismatched for a HLA loci, but similar to the ΝΙΜAs of the CBU, have a prognosis similar to 6/6-matched ones. Methods: The Hellenic Cord Blood Bank (HCBB) identified the maternal HLA of 380 cord blood donors, specifying the NIMA haplotypes of the related cryostored CBUs. Results: The HCBB extended the pool of HLA phenotypes through the generation of unique virtual phenotypes (VPs). A “VP database” was set up, using Microsoft Office—Access™, in order to provide NIMA-matched CBUs for potential recipients. The effectiveness of VPs’ matching was tested in 80 Greek patients. Conclusion: This methodology may contribute to the increase of the number of available CBUs for patients, in the case where there is no available CBU, or in case an additional one is needed. Through this method, the CBUs could be used faster and more effectively, rather than being cryostored for long periods of time.
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spelling pubmed-63163012019-01-10 Non-Inherited Maternal Antigens Identify Acceptable HLA Mismatches: A New Policy for the Hellenic Cord Blood Bank Panagouli, Effrosyni Dinou, Amalia Mallis, Panagiotis Michalopoulos, Efstathios Papassavas, Andreas Spyropoulou-Vlachou, Maria Meletis, John Angelopoulou, Maria Konstantopoulos, Kostas Vassilakopoulos, Theodoros Stavropoulos-Giokas, Catherine Bioengineering (Basel) Article Background: During pregnancy, the maternal-fetal contact may lead to the development of tolerance against the maternal human leukocyte antigen (HLA) that is not inherited by the fetus. These non-inherited maternal antigens (NIMAs) define acceptable HLA mismatches; therefore, the number of HLA phenotypes that are suitable matches for patients who need a hematopoietic stem cell transplant could be increased. Cord blood unit (CBU) transplantations to patients mismatched for a HLA loci, but similar to the ΝΙΜAs of the CBU, have a prognosis similar to 6/6-matched ones. Methods: The Hellenic Cord Blood Bank (HCBB) identified the maternal HLA of 380 cord blood donors, specifying the NIMA haplotypes of the related cryostored CBUs. Results: The HCBB extended the pool of HLA phenotypes through the generation of unique virtual phenotypes (VPs). A “VP database” was set up, using Microsoft Office—Access™, in order to provide NIMA-matched CBUs for potential recipients. The effectiveness of VPs’ matching was tested in 80 Greek patients. Conclusion: This methodology may contribute to the increase of the number of available CBUs for patients, in the case where there is no available CBU, or in case an additional one is needed. Through this method, the CBUs could be used faster and more effectively, rather than being cryostored for long periods of time. MDPI 2018-09-21 /pmc/articles/PMC6316301/ /pubmed/30248919 http://dx.doi.org/10.3390/bioengineering5040077 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Panagouli, Effrosyni
Dinou, Amalia
Mallis, Panagiotis
Michalopoulos, Efstathios
Papassavas, Andreas
Spyropoulou-Vlachou, Maria
Meletis, John
Angelopoulou, Maria
Konstantopoulos, Kostas
Vassilakopoulos, Theodoros
Stavropoulos-Giokas, Catherine
Non-Inherited Maternal Antigens Identify Acceptable HLA Mismatches: A New Policy for the Hellenic Cord Blood Bank
title Non-Inherited Maternal Antigens Identify Acceptable HLA Mismatches: A New Policy for the Hellenic Cord Blood Bank
title_full Non-Inherited Maternal Antigens Identify Acceptable HLA Mismatches: A New Policy for the Hellenic Cord Blood Bank
title_fullStr Non-Inherited Maternal Antigens Identify Acceptable HLA Mismatches: A New Policy for the Hellenic Cord Blood Bank
title_full_unstemmed Non-Inherited Maternal Antigens Identify Acceptable HLA Mismatches: A New Policy for the Hellenic Cord Blood Bank
title_short Non-Inherited Maternal Antigens Identify Acceptable HLA Mismatches: A New Policy for the Hellenic Cord Blood Bank
title_sort non-inherited maternal antigens identify acceptable hla mismatches: a new policy for the hellenic cord blood bank
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316301/
https://www.ncbi.nlm.nih.gov/pubmed/30248919
http://dx.doi.org/10.3390/bioengineering5040077
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