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Exploration of the association between the single-nucleotide polymorphism of co-stimulatory system and rheumatoid arthritis

INTRODUCTION: The human leukocyte antigen (HLA) has been linked to the majority of autoimmune diseases (ADs). However, non-HLA genes may be risk factors for ADs. A number of genes encoding proteins involved in regulating T-cell and B-cell function have been identified as rheumatoid arthritis (RA) su...

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Autores principales: Chen, Ding-Ping, Wen, Ying-Hao, Lin, Wei-Tzu, Hsu, Fang-Ping, Yu, Kuang-Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10344454/
https://www.ncbi.nlm.nih.gov/pubmed/37457686
http://dx.doi.org/10.3389/fimmu.2023.1123832
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author Chen, Ding-Ping
Wen, Ying-Hao
Lin, Wei-Tzu
Hsu, Fang-Ping
Yu, Kuang-Hui
author_facet Chen, Ding-Ping
Wen, Ying-Hao
Lin, Wei-Tzu
Hsu, Fang-Ping
Yu, Kuang-Hui
author_sort Chen, Ding-Ping
collection PubMed
description INTRODUCTION: The human leukocyte antigen (HLA) has been linked to the majority of autoimmune diseases (ADs). However, non-HLA genes may be risk factors for ADs. A number of genes encoding proteins involved in regulating T-cell and B-cell function have been identified as rheumatoid arthritis (RA) susceptibility genes. METHODS: In this study, we investigated the association between RA and single-nucleotide polymorphisms (SNPs) of co-stimulatory or co-inhibitory molecules in 124 RA cases and 100 healthy controls without immune-related diseases [including tumor necrosis factor superfamily member 4 (TNFSF4), CD28, cytotoxic T-lymphocyte–associated protein 4 (CTLA4), and programmed cell death protein 1 (PDCD1)]. RESULTS: The results showed that there were 13 SNPs associated with RA, including rs181758110 of TNFSF4 (CC vs. CT, p = 0.038); rs3181096 of CD28 (TT vs. CC + CT, p = 0.035; CC vs. TT, p = 0.047); rs11571315 (TT vs. CT, p = 0.045), rs733618 (CC vs. TT + CT, p = 0.043), rs4553808 (AA vs. AG vs. GG, p = 0.035), rs11571316 (GG vs. AG vs. AA, p = 0.048; GG vs. AG + AA, p = 0.026; GG vs. AG, p = 0.014), rs16840252 (CC vs. CT vs. TT, p = 0.007; CC vs. CT, p = 0.011), rs5742909 (CC vs. CT vs. TT, p = 0.040), and rs11571319 of CTLA4 (GG vs. AG vs. AA, p < 0.001; GG vs. AG + AA, p = 0.048; AA vs. GG + AG, p = 0.001; GG vs. AA, p = 0.008; GG vs. AG, p ≤ 0.001); and rs10204525 (TT vs. CT + CC, p = 0.024; TT vs. CT, p = 0.021), rs2227982 (AA vs. GG, p = 0.047), rs36084323 (TT vs. CT vs. CC, p = 0.022; TT vs. CT + CC, p = 0.013; CC vs. TT + CT, p = 0.048; TT vs. CC, p = 0.008), and rs5839828 of PDCD1 (DEL vs. DEL/G vs. GG, p = 0.014; DEL vs. DEL/G + GG, p = 0.014; GG vs. DEL + DEL/G, p = 0.025; DEL vs. GG, p = 0.007). DISCUSSION: Consequently, these SNPs may play an important role in immune regulation, and further research into the role of these SNPs of immune regulatory genes in the pathogenesis of RA is required.
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spelling pubmed-103444542023-07-14 Exploration of the association between the single-nucleotide polymorphism of co-stimulatory system and rheumatoid arthritis Chen, Ding-Ping Wen, Ying-Hao Lin, Wei-Tzu Hsu, Fang-Ping Yu, Kuang-Hui Front Immunol Immunology INTRODUCTION: The human leukocyte antigen (HLA) has been linked to the majority of autoimmune diseases (ADs). However, non-HLA genes may be risk factors for ADs. A number of genes encoding proteins involved in regulating T-cell and B-cell function have been identified as rheumatoid arthritis (RA) susceptibility genes. METHODS: In this study, we investigated the association between RA and single-nucleotide polymorphisms (SNPs) of co-stimulatory or co-inhibitory molecules in 124 RA cases and 100 healthy controls without immune-related diseases [including tumor necrosis factor superfamily member 4 (TNFSF4), CD28, cytotoxic T-lymphocyte–associated protein 4 (CTLA4), and programmed cell death protein 1 (PDCD1)]. RESULTS: The results showed that there were 13 SNPs associated with RA, including rs181758110 of TNFSF4 (CC vs. CT, p = 0.038); rs3181096 of CD28 (TT vs. CC + CT, p = 0.035; CC vs. TT, p = 0.047); rs11571315 (TT vs. CT, p = 0.045), rs733618 (CC vs. TT + CT, p = 0.043), rs4553808 (AA vs. AG vs. GG, p = 0.035), rs11571316 (GG vs. AG vs. AA, p = 0.048; GG vs. AG + AA, p = 0.026; GG vs. AG, p = 0.014), rs16840252 (CC vs. CT vs. TT, p = 0.007; CC vs. CT, p = 0.011), rs5742909 (CC vs. CT vs. TT, p = 0.040), and rs11571319 of CTLA4 (GG vs. AG vs. AA, p < 0.001; GG vs. AG + AA, p = 0.048; AA vs. GG + AG, p = 0.001; GG vs. AA, p = 0.008; GG vs. AG, p ≤ 0.001); and rs10204525 (TT vs. CT + CC, p = 0.024; TT vs. CT, p = 0.021), rs2227982 (AA vs. GG, p = 0.047), rs36084323 (TT vs. CT vs. CC, p = 0.022; TT vs. CT + CC, p = 0.013; CC vs. TT + CT, p = 0.048; TT vs. CC, p = 0.008), and rs5839828 of PDCD1 (DEL vs. DEL/G vs. GG, p = 0.014; DEL vs. DEL/G + GG, p = 0.014; GG vs. DEL + DEL/G, p = 0.025; DEL vs. GG, p = 0.007). DISCUSSION: Consequently, these SNPs may play an important role in immune regulation, and further research into the role of these SNPs of immune regulatory genes in the pathogenesis of RA is required. Frontiers Media S.A. 2023-06-29 /pmc/articles/PMC10344454/ /pubmed/37457686 http://dx.doi.org/10.3389/fimmu.2023.1123832 Text en Copyright © 2023 Chen, Wen, Lin, Hsu and Yu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Chen, Ding-Ping
Wen, Ying-Hao
Lin, Wei-Tzu
Hsu, Fang-Ping
Yu, Kuang-Hui
Exploration of the association between the single-nucleotide polymorphism of co-stimulatory system and rheumatoid arthritis
title Exploration of the association between the single-nucleotide polymorphism of co-stimulatory system and rheumatoid arthritis
title_full Exploration of the association between the single-nucleotide polymorphism of co-stimulatory system and rheumatoid arthritis
title_fullStr Exploration of the association between the single-nucleotide polymorphism of co-stimulatory system and rheumatoid arthritis
title_full_unstemmed Exploration of the association between the single-nucleotide polymorphism of co-stimulatory system and rheumatoid arthritis
title_short Exploration of the association between the single-nucleotide polymorphism of co-stimulatory system and rheumatoid arthritis
title_sort exploration of the association between the single-nucleotide polymorphism of co-stimulatory system and rheumatoid arthritis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10344454/
https://www.ncbi.nlm.nih.gov/pubmed/37457686
http://dx.doi.org/10.3389/fimmu.2023.1123832
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