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The Methylation in B7-H4 and BTLA Genes are Associated with the Risk of Pulmonary Tuberculosis

BACKGROUND: The important roles of B7 homologous body 4 (B7-H4), B and T lymphocyte attenuator (BTLA) in patients with pulmonary tuberculosis (PTB) have been reported. This study aims to evaluate the association among B7-H4 and BTLA genes polymorphism, methylation and PTB susceptibility. METHODOLOGY...

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Autores principales: Cai, Xue-Qian, Huang, Qian, Zhang, Tian-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683667/
https://www.ncbi.nlm.nih.gov/pubmed/38033484
http://dx.doi.org/10.2147/ITT.S434403
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author Cai, Xue-Qian
Huang, Qian
Zhang, Tian-Ping
author_facet Cai, Xue-Qian
Huang, Qian
Zhang, Tian-Ping
author_sort Cai, Xue-Qian
collection PubMed
description BACKGROUND: The important roles of B7 homologous body 4 (B7-H4), B and T lymphocyte attenuator (BTLA) in patients with pulmonary tuberculosis (PTB) have been reported. This study aims to evaluate the association among B7-H4 and BTLA genes polymorphism, methylation and PTB susceptibility. METHODOLOGY: Here, we assessed the possible relationship of 10 single nucleotide polymorphisms (SNPs) in B7-H4, BTLA genes with PTB susceptibility in a Chinese population (496 PTB patients and 502 controls) by SNPscan technique. Then, the B7-H4, BTLA genes methylation levels among 98 PTB patients and 97 controls were detected using MethylTarget technique. RESULTS: This study found no significant differences in allele and genotype frequencies of B7-H4 gene rs10754339, rs10801935, rs10923223, rs1937956, rs3738414, BTLA gene rs1982809, rs2971205, rs75368388, rs9288953 variants between PTB patients and controls. Haplotype analysis suggested that the lower frequencies of B7-H4 AATTG haplotype, BTLA GATT haplotype and the higher frequency of BTLA AGTC haplotype were found in PTB patients when compared with controls. We also found that the frequency of BTLA gene rs9288953 C allele was significantly increased in PTB patients with drug resistance. Moreover, the methylation levels of B7-H4 and BTLA genes in PTB patients were greater than that in controls, and rs10754339 variant in B7-H4 gene could affect its methylation level in PTB patients. CONCLUSION: B7-H4, BTLA genes polymorphism might not affect PTB susceptibility, while the abnormal methylation levels of B7-H4, BTLA genes were associated with the genetic background of PTB.
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spelling pubmed-106836672023-11-30 The Methylation in B7-H4 and BTLA Genes are Associated with the Risk of Pulmonary Tuberculosis Cai, Xue-Qian Huang, Qian Zhang, Tian-Ping Immunotargets Ther Original Research BACKGROUND: The important roles of B7 homologous body 4 (B7-H4), B and T lymphocyte attenuator (BTLA) in patients with pulmonary tuberculosis (PTB) have been reported. This study aims to evaluate the association among B7-H4 and BTLA genes polymorphism, methylation and PTB susceptibility. METHODOLOGY: Here, we assessed the possible relationship of 10 single nucleotide polymorphisms (SNPs) in B7-H4, BTLA genes with PTB susceptibility in a Chinese population (496 PTB patients and 502 controls) by SNPscan technique. Then, the B7-H4, BTLA genes methylation levels among 98 PTB patients and 97 controls were detected using MethylTarget technique. RESULTS: This study found no significant differences in allele and genotype frequencies of B7-H4 gene rs10754339, rs10801935, rs10923223, rs1937956, rs3738414, BTLA gene rs1982809, rs2971205, rs75368388, rs9288953 variants between PTB patients and controls. Haplotype analysis suggested that the lower frequencies of B7-H4 AATTG haplotype, BTLA GATT haplotype and the higher frequency of BTLA AGTC haplotype were found in PTB patients when compared with controls. We also found that the frequency of BTLA gene rs9288953 C allele was significantly increased in PTB patients with drug resistance. Moreover, the methylation levels of B7-H4 and BTLA genes in PTB patients were greater than that in controls, and rs10754339 variant in B7-H4 gene could affect its methylation level in PTB patients. CONCLUSION: B7-H4, BTLA genes polymorphism might not affect PTB susceptibility, while the abnormal methylation levels of B7-H4, BTLA genes were associated with the genetic background of PTB. Dove 2023-11-24 /pmc/articles/PMC10683667/ /pubmed/38033484 http://dx.doi.org/10.2147/ITT.S434403 Text en © 2023 Cai et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Cai, Xue-Qian
Huang, Qian
Zhang, Tian-Ping
The Methylation in B7-H4 and BTLA Genes are Associated with the Risk of Pulmonary Tuberculosis
title The Methylation in B7-H4 and BTLA Genes are Associated with the Risk of Pulmonary Tuberculosis
title_full The Methylation in B7-H4 and BTLA Genes are Associated with the Risk of Pulmonary Tuberculosis
title_fullStr The Methylation in B7-H4 and BTLA Genes are Associated with the Risk of Pulmonary Tuberculosis
title_full_unstemmed The Methylation in B7-H4 and BTLA Genes are Associated with the Risk of Pulmonary Tuberculosis
title_short The Methylation in B7-H4 and BTLA Genes are Associated with the Risk of Pulmonary Tuberculosis
title_sort methylation in b7-h4 and btla genes are associated with the risk of pulmonary tuberculosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683667/
https://www.ncbi.nlm.nih.gov/pubmed/38033484
http://dx.doi.org/10.2147/ITT.S434403
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