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Exploring the association between Th17 pathway gene polymorphisms and pulmonary tuberculosis

Th17 cells play a key role in immunity against Mycobacterium tuberculosis (MTB), and this study aimed to explore the association of Th17 pathway gene polymorphisms with pulmonary tuberculosis (PTB) susceptibility in a Chinese population. A total of 10 single nucleotide polymorphisms in Th17 pathway...

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Autores principales: Li, Hong-Miao, Wang, Li-Jun, Huang, Qian, Pan, Hai-Feng, Zhang, Tian-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723456/
https://www.ncbi.nlm.nih.gov/pubmed/36483566
http://dx.doi.org/10.3389/fimmu.2022.994247
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author Li, Hong-Miao
Wang, Li-Jun
Huang, Qian
Pan, Hai-Feng
Zhang, Tian-Ping
author_facet Li, Hong-Miao
Wang, Li-Jun
Huang, Qian
Pan, Hai-Feng
Zhang, Tian-Ping
author_sort Li, Hong-Miao
collection PubMed
description Th17 cells play a key role in immunity against Mycobacterium tuberculosis (MTB), and this study aimed to explore the association of Th17 pathway gene polymorphisms with pulmonary tuberculosis (PTB) susceptibility in a Chinese population. A total of 10 single nucleotide polymorphisms in Th17 pathway genes (IL-17A gene rs2275913, rs3748067, rs8193036, rs3819024, IL-17F gene rs7741835, rs763780, IL-21 gene rs907715, rs2055979, IL-23R gene rs11805303, and rs7518660) were genotyped in 456 PTB patients and 466 controls using SNPscan technique. The IL-23R rs11805303 CC genotype, C allele frequencies were significantly lower in PTB patients than in controls, and the rs11805303 variant was significantly associated with the reduced risk of PTB in a recessive model. There were no significant associations between IL-17A, IL-17F, and IL-21 gene variations and PTB risk. In IL-17A gene, rs2275913, rs3748067, and rs3819024 variants were associated with drug resistance in PTB patients. In IL-17F gene, rs7741835 variant affected drug resistance, and rs763780 variant was associated with hypoproteinemia in PTB patients. In addition, the lower frequencies of the TT genotype, T allele of rs2055979 were found in PTB patients with drug-induced liver injury. Haplotype analysis showed that IL-23R CG haplotype frequency was significantly lower in PTB patients than in controls, while the TG haplotype frequency was higher. In conclusion, IL-23R rs11805303 polymorphism may contribute to the genetic underpinnings of PTB in the Chinese population, and the IL-17A, IL-17F, and IL-21 genetic variations are associated with several clinical manifestations of PTB patients.
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spelling pubmed-97234562022-12-07 Exploring the association between Th17 pathway gene polymorphisms and pulmonary tuberculosis Li, Hong-Miao Wang, Li-Jun Huang, Qian Pan, Hai-Feng Zhang, Tian-Ping Front Immunol Immunology Th17 cells play a key role in immunity against Mycobacterium tuberculosis (MTB), and this study aimed to explore the association of Th17 pathway gene polymorphisms with pulmonary tuberculosis (PTB) susceptibility in a Chinese population. A total of 10 single nucleotide polymorphisms in Th17 pathway genes (IL-17A gene rs2275913, rs3748067, rs8193036, rs3819024, IL-17F gene rs7741835, rs763780, IL-21 gene rs907715, rs2055979, IL-23R gene rs11805303, and rs7518660) were genotyped in 456 PTB patients and 466 controls using SNPscan technique. The IL-23R rs11805303 CC genotype, C allele frequencies were significantly lower in PTB patients than in controls, and the rs11805303 variant was significantly associated with the reduced risk of PTB in a recessive model. There were no significant associations between IL-17A, IL-17F, and IL-21 gene variations and PTB risk. In IL-17A gene, rs2275913, rs3748067, and rs3819024 variants were associated with drug resistance in PTB patients. In IL-17F gene, rs7741835 variant affected drug resistance, and rs763780 variant was associated with hypoproteinemia in PTB patients. In addition, the lower frequencies of the TT genotype, T allele of rs2055979 were found in PTB patients with drug-induced liver injury. Haplotype analysis showed that IL-23R CG haplotype frequency was significantly lower in PTB patients than in controls, while the TG haplotype frequency was higher. In conclusion, IL-23R rs11805303 polymorphism may contribute to the genetic underpinnings of PTB in the Chinese population, and the IL-17A, IL-17F, and IL-21 genetic variations are associated with several clinical manifestations of PTB patients. Frontiers Media S.A. 2022-11-21 /pmc/articles/PMC9723456/ /pubmed/36483566 http://dx.doi.org/10.3389/fimmu.2022.994247 Text en Copyright © 2022 Li, Wang, Huang, Pan and Zhang 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
Li, Hong-Miao
Wang, Li-Jun
Huang, Qian
Pan, Hai-Feng
Zhang, Tian-Ping
Exploring the association between Th17 pathway gene polymorphisms and pulmonary tuberculosis
title Exploring the association between Th17 pathway gene polymorphisms and pulmonary tuberculosis
title_full Exploring the association between Th17 pathway gene polymorphisms and pulmonary tuberculosis
title_fullStr Exploring the association between Th17 pathway gene polymorphisms and pulmonary tuberculosis
title_full_unstemmed Exploring the association between Th17 pathway gene polymorphisms and pulmonary tuberculosis
title_short Exploring the association between Th17 pathway gene polymorphisms and pulmonary tuberculosis
title_sort exploring the association between th17 pathway gene polymorphisms and pulmonary tuberculosis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723456/
https://www.ncbi.nlm.nih.gov/pubmed/36483566
http://dx.doi.org/10.3389/fimmu.2022.994247
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