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Toll-like receptor genetic variations in bone marrow transplantation

The Toll-like receptor family mediates the innate immune system through recognizing the molecular patterns of microorganisms and self-components and leading the synthesis of the inflammatory mediators. We retrospectively examined whether or not genetic variations in toll-like receptor 1 (rs5743551,...

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Autores principales: Uchino, Kaori, Mizuno, Shohei, Sato-Otsubo, Aiko, Nannya, Yasuhito, Mizutani, Motonori, Horio, Tomohiro, Hanamura, Ichiro, Espinoza, J. Luis, Onizuka, Makoto, Kashiwase, Koichi, Morishima, Yasuo, Fukuda, Takahiro, Kodera, Yoshihisa, Doki, Noriko, Miyamura, Koichi, Mori, Takehiko, Ogawa, Seishi, Takami, Akiyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542217/
https://www.ncbi.nlm.nih.gov/pubmed/28484092
http://dx.doi.org/10.18632/oncotarget.17315
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author Uchino, Kaori
Mizuno, Shohei
Sato-Otsubo, Aiko
Nannya, Yasuhito
Mizutani, Motonori
Horio, Tomohiro
Hanamura, Ichiro
Espinoza, J. Luis
Onizuka, Makoto
Kashiwase, Koichi
Morishima, Yasuo
Fukuda, Takahiro
Kodera, Yoshihisa
Doki, Noriko
Miyamura, Koichi
Mori, Takehiko
Ogawa, Seishi
Takami, Akiyoshi
author_facet Uchino, Kaori
Mizuno, Shohei
Sato-Otsubo, Aiko
Nannya, Yasuhito
Mizutani, Motonori
Horio, Tomohiro
Hanamura, Ichiro
Espinoza, J. Luis
Onizuka, Makoto
Kashiwase, Koichi
Morishima, Yasuo
Fukuda, Takahiro
Kodera, Yoshihisa
Doki, Noriko
Miyamura, Koichi
Mori, Takehiko
Ogawa, Seishi
Takami, Akiyoshi
author_sort Uchino, Kaori
collection PubMed
description The Toll-like receptor family mediates the innate immune system through recognizing the molecular patterns of microorganisms and self-components and leading the synthesis of the inflammatory mediators. We retrospectively examined whether or not genetic variations in toll-like receptor 1 (rs5743551, -7202GQ>A), toll-like receptor 2 (rs7656411, 22215G>T), and toll-like receptor 4 (rs11536889, +3725G>C) affected transplant outcomes in a cohort of 365 patients who underwent unrelated HLA-matched bone marrow transplantation (for hematologic malignancies through the Japan Marrow Donor Program. Only donor toll-like receptor 4 variation significantly improved the survival outcomes. A multivariate analysis showed that the donor toll-like receptor 4 +3725G/G genotype was significantly associated with a better 5-year progression-free survival and a lower 5-year transplant-related mortality than other variations. Furthermore, the donor toll-like receptor 4 +3725G/G genotype was associated with a significantly lower incidence of fatal infections than other variations. The validation study of 502 patients confirmed that the donor toll-like receptor 4 +3725G/G genotype was associated with better survival outcomes. Toll-like receptor4 genotyping in transplant donors may therefore be a useful tool for optimizing donor selection and evaluating pretransplantation risks.
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spelling pubmed-55422172017-08-07 Toll-like receptor genetic variations in bone marrow transplantation Uchino, Kaori Mizuno, Shohei Sato-Otsubo, Aiko Nannya, Yasuhito Mizutani, Motonori Horio, Tomohiro Hanamura, Ichiro Espinoza, J. Luis Onizuka, Makoto Kashiwase, Koichi Morishima, Yasuo Fukuda, Takahiro Kodera, Yoshihisa Doki, Noriko Miyamura, Koichi Mori, Takehiko Ogawa, Seishi Takami, Akiyoshi Oncotarget Research Paper The Toll-like receptor family mediates the innate immune system through recognizing the molecular patterns of microorganisms and self-components and leading the synthesis of the inflammatory mediators. We retrospectively examined whether or not genetic variations in toll-like receptor 1 (rs5743551, -7202GQ>A), toll-like receptor 2 (rs7656411, 22215G>T), and toll-like receptor 4 (rs11536889, +3725G>C) affected transplant outcomes in a cohort of 365 patients who underwent unrelated HLA-matched bone marrow transplantation (for hematologic malignancies through the Japan Marrow Donor Program. Only donor toll-like receptor 4 variation significantly improved the survival outcomes. A multivariate analysis showed that the donor toll-like receptor 4 +3725G/G genotype was significantly associated with a better 5-year progression-free survival and a lower 5-year transplant-related mortality than other variations. Furthermore, the donor toll-like receptor 4 +3725G/G genotype was associated with a significantly lower incidence of fatal infections than other variations. The validation study of 502 patients confirmed that the donor toll-like receptor 4 +3725G/G genotype was associated with better survival outcomes. Toll-like receptor4 genotyping in transplant donors may therefore be a useful tool for optimizing donor selection and evaluating pretransplantation risks. Impact Journals LLC 2017-04-21 /pmc/articles/PMC5542217/ /pubmed/28484092 http://dx.doi.org/10.18632/oncotarget.17315 Text en Copyright: © 2017 Uchino et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Uchino, Kaori
Mizuno, Shohei
Sato-Otsubo, Aiko
Nannya, Yasuhito
Mizutani, Motonori
Horio, Tomohiro
Hanamura, Ichiro
Espinoza, J. Luis
Onizuka, Makoto
Kashiwase, Koichi
Morishima, Yasuo
Fukuda, Takahiro
Kodera, Yoshihisa
Doki, Noriko
Miyamura, Koichi
Mori, Takehiko
Ogawa, Seishi
Takami, Akiyoshi
Toll-like receptor genetic variations in bone marrow transplantation
title Toll-like receptor genetic variations in bone marrow transplantation
title_full Toll-like receptor genetic variations in bone marrow transplantation
title_fullStr Toll-like receptor genetic variations in bone marrow transplantation
title_full_unstemmed Toll-like receptor genetic variations in bone marrow transplantation
title_short Toll-like receptor genetic variations in bone marrow transplantation
title_sort toll-like receptor genetic variations in bone marrow transplantation
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542217/
https://www.ncbi.nlm.nih.gov/pubmed/28484092
http://dx.doi.org/10.18632/oncotarget.17315
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