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The cytokine polymorphisms affecting Th1/Th2 increase the susceptibility to, and severity of, chronic ITP

BACKGROUND: T-helper cell type 1 (Th1) polarization in chronic immune thrombocytopenia (cITP) has been reported at the protein and mRNA levels. We evaluated the impact of Th1/Th2 cytokine and cytokine receptor functional polymorphisms on both susceptibility to, and severity of, cITP. We analysed IFN...

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Autores principales: Takahashi, Noriyuki, Saitoh, Takayuki, Gotoh, Nanami, Nitta, Yasuhiro, Alkebsi, Lobna, Kasamatsu, Tetsuhiro, Minato, Yusuke, Yokohama, Akihiko, Tsukamoto, Norifumi, Handa, Hiroshi, Murakami, Hirokazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434613/
https://www.ncbi.nlm.nih.gov/pubmed/28511637
http://dx.doi.org/10.1186/s12865-017-0210-3
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author Takahashi, Noriyuki
Saitoh, Takayuki
Gotoh, Nanami
Nitta, Yasuhiro
Alkebsi, Lobna
Kasamatsu, Tetsuhiro
Minato, Yusuke
Yokohama, Akihiko
Tsukamoto, Norifumi
Handa, Hiroshi
Murakami, Hirokazu
author_facet Takahashi, Noriyuki
Saitoh, Takayuki
Gotoh, Nanami
Nitta, Yasuhiro
Alkebsi, Lobna
Kasamatsu, Tetsuhiro
Minato, Yusuke
Yokohama, Akihiko
Tsukamoto, Norifumi
Handa, Hiroshi
Murakami, Hirokazu
author_sort Takahashi, Noriyuki
collection PubMed
description BACKGROUND: T-helper cell type 1 (Th1) polarization in chronic immune thrombocytopenia (cITP) has been reported at the protein and mRNA levels. We evaluated the impact of Th1/Th2 cytokine and cytokine receptor functional polymorphisms on both susceptibility to, and severity of, cITP. We analysed IFN-γ + 874 T/A, IFN-γR -611G/A, IL-4 -590C/T, and IL-4Rα Q576R polymorphisms in 126 cITP patients (male/female: 34/92; median age: 47.7 years) and 202 healthy control donors. Genotyping was determined by PCR and direct sequencing. The Th1/Th2 ratio was detected in peripheral blood mononuclear cells via flow cytometry. RESULTS: cITP patients had a higher frequency of the IL-4Rα 576 non-QQ genotype compared to healthy subjects (P = 0.04). cITP patients with the IFN-γ +874 non-AA genotype (high expression type) showed more severe thrombocytopenia than those with the AA genotype (P < 0.05). cITP patients had a significantly higher Th1/Th2 ratio than control patients (P < 0.01); this ratio was inversely correlated with platelet counts. Furthermore, patients with both IFN-γ +874 non-AA genotype (high expression type) and IFN-γR −611 non-AA genotype (high-function type) had a significantly higher Th1/Th2 ratio (P < 0.05). CONCLUSIONS: The cytokine polymorphisms affecting Th1/Th2 increase the susceptibility to, and severity of, chronic ITP.
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spelling pubmed-54346132017-05-18 The cytokine polymorphisms affecting Th1/Th2 increase the susceptibility to, and severity of, chronic ITP Takahashi, Noriyuki Saitoh, Takayuki Gotoh, Nanami Nitta, Yasuhiro Alkebsi, Lobna Kasamatsu, Tetsuhiro Minato, Yusuke Yokohama, Akihiko Tsukamoto, Norifumi Handa, Hiroshi Murakami, Hirokazu BMC Immunol Research Article BACKGROUND: T-helper cell type 1 (Th1) polarization in chronic immune thrombocytopenia (cITP) has been reported at the protein and mRNA levels. We evaluated the impact of Th1/Th2 cytokine and cytokine receptor functional polymorphisms on both susceptibility to, and severity of, cITP. We analysed IFN-γ + 874 T/A, IFN-γR -611G/A, IL-4 -590C/T, and IL-4Rα Q576R polymorphisms in 126 cITP patients (male/female: 34/92; median age: 47.7 years) and 202 healthy control donors. Genotyping was determined by PCR and direct sequencing. The Th1/Th2 ratio was detected in peripheral blood mononuclear cells via flow cytometry. RESULTS: cITP patients had a higher frequency of the IL-4Rα 576 non-QQ genotype compared to healthy subjects (P = 0.04). cITP patients with the IFN-γ +874 non-AA genotype (high expression type) showed more severe thrombocytopenia than those with the AA genotype (P < 0.05). cITP patients had a significantly higher Th1/Th2 ratio than control patients (P < 0.01); this ratio was inversely correlated with platelet counts. Furthermore, patients with both IFN-γ +874 non-AA genotype (high expression type) and IFN-γR −611 non-AA genotype (high-function type) had a significantly higher Th1/Th2 ratio (P < 0.05). CONCLUSIONS: The cytokine polymorphisms affecting Th1/Th2 increase the susceptibility to, and severity of, chronic ITP. BioMed Central 2017-05-16 /pmc/articles/PMC5434613/ /pubmed/28511637 http://dx.doi.org/10.1186/s12865-017-0210-3 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Takahashi, Noriyuki
Saitoh, Takayuki
Gotoh, Nanami
Nitta, Yasuhiro
Alkebsi, Lobna
Kasamatsu, Tetsuhiro
Minato, Yusuke
Yokohama, Akihiko
Tsukamoto, Norifumi
Handa, Hiroshi
Murakami, Hirokazu
The cytokine polymorphisms affecting Th1/Th2 increase the susceptibility to, and severity of, chronic ITP
title The cytokine polymorphisms affecting Th1/Th2 increase the susceptibility to, and severity of, chronic ITP
title_full The cytokine polymorphisms affecting Th1/Th2 increase the susceptibility to, and severity of, chronic ITP
title_fullStr The cytokine polymorphisms affecting Th1/Th2 increase the susceptibility to, and severity of, chronic ITP
title_full_unstemmed The cytokine polymorphisms affecting Th1/Th2 increase the susceptibility to, and severity of, chronic ITP
title_short The cytokine polymorphisms affecting Th1/Th2 increase the susceptibility to, and severity of, chronic ITP
title_sort cytokine polymorphisms affecting th1/th2 increase the susceptibility to, and severity of, chronic itp
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434613/
https://www.ncbi.nlm.nih.gov/pubmed/28511637
http://dx.doi.org/10.1186/s12865-017-0210-3
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