Association between interleukin-10 polymorphisms and CD4+CD25+FOXP3+ T cells in asthmatic children
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Jornal de Pediatria (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572021000500546 |
Resumo: | Abstract Objective: The aim of this study was to evaluate the association between possible functional interleukin-10 (IL-10) polymorphisms, IL-10 expression and regulatory T cells (Tregs) frequency, and/or asthma severity in a sample of children and adolescents. Methods: This is a nested case-control genetic association study. The study sample consisted of children and adolescents aged 8–14 from public schools. Four polymorphisms of the IL-10 gene (rs1518111, rs3024490, rs3024496, rs3024491) were genotyped in asthmatic subjects and controls using real-time PCR. Tregs cells and IL-10 were analyzed in peripheral blood mononuclear cells by flow cytometry. The severity of asthma was defined according to the Global Initiative for Asthma (GINA) guideline. Results: One hundred twenty-three asthmatic subjects and fifty-eight controls participated in the study. The single nucleotide polymorphism (SNP) rs3024491 (T allele) showed association with asthma severity, presenting a higher frequency in patients in the moderate asthma group. The T allele of variant rs3024491 also showed an association with reduced IL-10 levels (p = 0.01) and with increased Tregs frequency (p = 0.01). The other variants did not present consistent associations. Conclusions: Our results suggest that moderate asthma is associated with a higher frequency of the T allele in the SNP rs3024491. In addition, the variant rs3024491 (TT) was associated with a reduction in IL-10 production and an increased percentage of Tregs cells, suggesting possible mechanisms that influence asthma severity. |
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Jornal de Pediatria (Online) |
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Association between interleukin-10 polymorphisms and CD4+CD25+FOXP3+ T cells in asthmatic childrenAsthmaChildren and adolescentsImmunologyInterleukin-10PolymorphismRegulatory T cellsAbstract Objective: The aim of this study was to evaluate the association between possible functional interleukin-10 (IL-10) polymorphisms, IL-10 expression and regulatory T cells (Tregs) frequency, and/or asthma severity in a sample of children and adolescents. Methods: This is a nested case-control genetic association study. The study sample consisted of children and adolescents aged 8–14 from public schools. Four polymorphisms of the IL-10 gene (rs1518111, rs3024490, rs3024496, rs3024491) were genotyped in asthmatic subjects and controls using real-time PCR. Tregs cells and IL-10 were analyzed in peripheral blood mononuclear cells by flow cytometry. The severity of asthma was defined according to the Global Initiative for Asthma (GINA) guideline. Results: One hundred twenty-three asthmatic subjects and fifty-eight controls participated in the study. The single nucleotide polymorphism (SNP) rs3024491 (T allele) showed association with asthma severity, presenting a higher frequency in patients in the moderate asthma group. The T allele of variant rs3024491 also showed an association with reduced IL-10 levels (p = 0.01) and with increased Tregs frequency (p = 0.01). The other variants did not present consistent associations. Conclusions: Our results suggest that moderate asthma is associated with a higher frequency of the T allele in the SNP rs3024491. In addition, the variant rs3024491 (TT) was associated with a reduction in IL-10 production and an increased percentage of Tregs cells, suggesting possible mechanisms that influence asthma severity.Sociedade Brasileira de Pediatria2021-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572021000500546Jornal de Pediatria v.97 n.5 2021reponame:Jornal de Pediatria (Online)instname:Sociedade Brasileira de Pediatria (SBP)instacron:SBPE10.1016/j.jped.2020.11.008info:eu-repo/semantics/openAccessMocellin,MagáliLeitão,Lidiane Alves de AzeredoAraújo,Patrícia Dias deJones,Marcus HerbertStein,Renato TetelbomPitrez,Paulo MárcioSouza,Ana Paula Duarte dePinto,Leonardo Araújoeng2021-10-08T00:00:00Zoai:scielo:S0021-75572021000500546Revistahttp://www.jped.com.br/https://old.scielo.br/oai/scielo-oai.php||jped@jped.com.br1678-47820021-7557opendoar:2021-10-08T00:00Jornal de Pediatria (Online) - Sociedade Brasileira de Pediatria (SBP)false |
dc.title.none.fl_str_mv |
Association between interleukin-10 polymorphisms and CD4+CD25+FOXP3+ T cells in asthmatic children |
title |
Association between interleukin-10 polymorphisms and CD4+CD25+FOXP3+ T cells in asthmatic children |
spellingShingle |
Association between interleukin-10 polymorphisms and CD4+CD25+FOXP3+ T cells in asthmatic children Mocellin,Magáli Asthma Children and adolescents Immunology Interleukin-10 Polymorphism Regulatory T cells |
title_short |
Association between interleukin-10 polymorphisms and CD4+CD25+FOXP3+ T cells in asthmatic children |
title_full |
Association between interleukin-10 polymorphisms and CD4+CD25+FOXP3+ T cells in asthmatic children |
title_fullStr |
Association between interleukin-10 polymorphisms and CD4+CD25+FOXP3+ T cells in asthmatic children |
title_full_unstemmed |
Association between interleukin-10 polymorphisms and CD4+CD25+FOXP3+ T cells in asthmatic children |
title_sort |
Association between interleukin-10 polymorphisms and CD4+CD25+FOXP3+ T cells in asthmatic children |
author |
Mocellin,Magáli |
author_facet |
Mocellin,Magáli Leitão,Lidiane Alves de Azeredo Araújo,Patrícia Dias de Jones,Marcus Herbert Stein,Renato Tetelbom Pitrez,Paulo Márcio Souza,Ana Paula Duarte de Pinto,Leonardo Araújo |
author_role |
author |
author2 |
Leitão,Lidiane Alves de Azeredo Araújo,Patrícia Dias de Jones,Marcus Herbert Stein,Renato Tetelbom Pitrez,Paulo Márcio Souza,Ana Paula Duarte de Pinto,Leonardo Araújo |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Mocellin,Magáli Leitão,Lidiane Alves de Azeredo Araújo,Patrícia Dias de Jones,Marcus Herbert Stein,Renato Tetelbom Pitrez,Paulo Márcio Souza,Ana Paula Duarte de Pinto,Leonardo Araújo |
dc.subject.por.fl_str_mv |
Asthma Children and adolescents Immunology Interleukin-10 Polymorphism Regulatory T cells |
topic |
Asthma Children and adolescents Immunology Interleukin-10 Polymorphism Regulatory T cells |
description |
Abstract Objective: The aim of this study was to evaluate the association between possible functional interleukin-10 (IL-10) polymorphisms, IL-10 expression and regulatory T cells (Tregs) frequency, and/or asthma severity in a sample of children and adolescents. Methods: This is a nested case-control genetic association study. The study sample consisted of children and adolescents aged 8–14 from public schools. Four polymorphisms of the IL-10 gene (rs1518111, rs3024490, rs3024496, rs3024491) were genotyped in asthmatic subjects and controls using real-time PCR. Tregs cells and IL-10 were analyzed in peripheral blood mononuclear cells by flow cytometry. The severity of asthma was defined according to the Global Initiative for Asthma (GINA) guideline. Results: One hundred twenty-three asthmatic subjects and fifty-eight controls participated in the study. The single nucleotide polymorphism (SNP) rs3024491 (T allele) showed association with asthma severity, presenting a higher frequency in patients in the moderate asthma group. The T allele of variant rs3024491 also showed an association with reduced IL-10 levels (p = 0.01) and with increased Tregs frequency (p = 0.01). The other variants did not present consistent associations. Conclusions: Our results suggest that moderate asthma is associated with a higher frequency of the T allele in the SNP rs3024491. In addition, the variant rs3024491 (TT) was associated with a reduction in IL-10 production and an increased percentage of Tregs cells, suggesting possible mechanisms that influence asthma severity. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-10-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572021000500546 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572021000500546 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1016/j.jped.2020.11.008 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Pediatria |
publisher.none.fl_str_mv |
Sociedade Brasileira de Pediatria |
dc.source.none.fl_str_mv |
Jornal de Pediatria v.97 n.5 2021 reponame:Jornal de Pediatria (Online) instname:Sociedade Brasileira de Pediatria (SBP) instacron:SBPE |
instname_str |
Sociedade Brasileira de Pediatria (SBP) |
instacron_str |
SBPE |
institution |
SBPE |
reponame_str |
Jornal de Pediatria (Online) |
collection |
Jornal de Pediatria (Online) |
repository.name.fl_str_mv |
Jornal de Pediatria (Online) - Sociedade Brasileira de Pediatria (SBP) |
repository.mail.fl_str_mv |
||jped@jped.com.br |
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1752122322818433024 |