Polymorphism analysis of the CTLA-4 gene in paracoccidioidomycosis patients
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Memórias do Instituto Oswaldo Cruz |
Texto Completo: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762011000200017 |
Resumo: | The CTLA-4 protein is expressed in activated T cells and plays an essential role in the immune response through its regulatory effect on T cell activation. Polymorphisms of the CTLA-4 gene have been correlated with autoimmune, neoplastic and infectious illnesses. This work aimed to verify possible associations between single nucleotide polymorphisms (SNPs) in CTLA-4, -318C/T in the promoter and +49A/G in exon 1 and paracoccidioidomycosis (PCM) caused by Paracoccidioides brasiliensis. For this purpose, 66 chronic form PCM patients and 76 healthy controls had their allele, genotype and haplotype frequencies determined. The genetic admixture structure of the patients and controls was evaluated to eliminate ancestral bias. The comparison of frequencies indicated no significant differences between patients and controls that could link the SNPs to PCM. Groups were admixture matched with no difference observed in population ancestry inference, indicating that the absence of association between CTLA-4 polymorphisms and PCM could not be attributed to ancestral bias. This study showed that there was no association between the CTLA-4 SNPs -318 and +49 and the resistance or susceptibility to PCM. |
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Memórias do Instituto Oswaldo Cruz |
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Polymorphism analysis of the CTLA-4 gene in paracoccidioidomycosis patientsadmixtureBrazilian populationhaplotypesParacoccidioides brasiliensisPCMsingle nucleotide polymorphismThe CTLA-4 protein is expressed in activated T cells and plays an essential role in the immune response through its regulatory effect on T cell activation. Polymorphisms of the CTLA-4 gene have been correlated with autoimmune, neoplastic and infectious illnesses. This work aimed to verify possible associations between single nucleotide polymorphisms (SNPs) in CTLA-4, -318C/T in the promoter and +49A/G in exon 1 and paracoccidioidomycosis (PCM) caused by Paracoccidioides brasiliensis. For this purpose, 66 chronic form PCM patients and 76 healthy controls had their allele, genotype and haplotype frequencies determined. The genetic admixture structure of the patients and controls was evaluated to eliminate ancestral bias. The comparison of frequencies indicated no significant differences between patients and controls that could link the SNPs to PCM. Groups were admixture matched with no difference observed in population ancestry inference, indicating that the absence of association between CTLA-4 polymorphisms and PCM could not be attributed to ancestral bias. This study showed that there was no association between the CTLA-4 SNPs -318 and +49 and the resistance or susceptibility to PCM.Instituto Oswaldo Cruz, Ministério da Saúde2011-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762011000200017Memórias do Instituto Oswaldo Cruz v.106 n.2 2011reponame:Memórias do Instituto Oswaldo Cruzinstname:Fundação Oswaldo Cruzinstacron:FIOCRUZ10.1590/S0074-02762011000200017info:eu-repo/semantics/openAccessLozano,Viviane FLins,Tulio CTeixeira,Marcus MVieira,Rodrigo GBlotta,Maria Heloisa SLGoes,Alfredo MSilva,Izabel Cristina RPereira,Rinaldo WBocca,Anamelia LFelipe,Maria Sueli Seng2020-04-25T17:50:59Zhttp://www.scielo.br/oai/scielo-oai.php0074-02761678-8060opendoar:null2020-04-26 02:17:32.211Memórias do Instituto Oswaldo Cruz - Fundação Oswaldo Cruztrue |
dc.title.none.fl_str_mv |
Polymorphism analysis of the CTLA-4 gene in paracoccidioidomycosis patients |
title |
Polymorphism analysis of the CTLA-4 gene in paracoccidioidomycosis patients |
spellingShingle |
Polymorphism analysis of the CTLA-4 gene in paracoccidioidomycosis patients Lozano,Viviane F admixture Brazilian population haplotypes Paracoccidioides brasiliensis PCM single nucleotide polymorphism |
title_short |
Polymorphism analysis of the CTLA-4 gene in paracoccidioidomycosis patients |
title_full |
Polymorphism analysis of the CTLA-4 gene in paracoccidioidomycosis patients |
title_fullStr |
Polymorphism analysis of the CTLA-4 gene in paracoccidioidomycosis patients |
title_full_unstemmed |
Polymorphism analysis of the CTLA-4 gene in paracoccidioidomycosis patients |
title_sort |
Polymorphism analysis of the CTLA-4 gene in paracoccidioidomycosis patients |
author |
Lozano,Viviane F |
author_facet |
Lozano,Viviane F Lins,Tulio C Teixeira,Marcus M Vieira,Rodrigo G Blotta,Maria Heloisa SL Goes,Alfredo M Silva,Izabel Cristina R Pereira,Rinaldo W Bocca,Anamelia L Felipe,Maria Sueli S |
author_role |
author |
author2 |
Lins,Tulio C Teixeira,Marcus M Vieira,Rodrigo G Blotta,Maria Heloisa SL Goes,Alfredo M Silva,Izabel Cristina R Pereira,Rinaldo W Bocca,Anamelia L Felipe,Maria Sueli S |
author2_role |
author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Lozano,Viviane F Lins,Tulio C Teixeira,Marcus M Vieira,Rodrigo G Blotta,Maria Heloisa SL Goes,Alfredo M Silva,Izabel Cristina R Pereira,Rinaldo W Bocca,Anamelia L Felipe,Maria Sueli S |
dc.subject.por.fl_str_mv |
admixture Brazilian population haplotypes Paracoccidioides brasiliensis PCM single nucleotide polymorphism |
topic |
admixture Brazilian population haplotypes Paracoccidioides brasiliensis PCM single nucleotide polymorphism |
dc.description.none.fl_txt_mv |
The CTLA-4 protein is expressed in activated T cells and plays an essential role in the immune response through its regulatory effect on T cell activation. Polymorphisms of the CTLA-4 gene have been correlated with autoimmune, neoplastic and infectious illnesses. This work aimed to verify possible associations between single nucleotide polymorphisms (SNPs) in CTLA-4, -318C/T in the promoter and +49A/G in exon 1 and paracoccidioidomycosis (PCM) caused by Paracoccidioides brasiliensis. For this purpose, 66 chronic form PCM patients and 76 healthy controls had their allele, genotype and haplotype frequencies determined. The genetic admixture structure of the patients and controls was evaluated to eliminate ancestral bias. The comparison of frequencies indicated no significant differences between patients and controls that could link the SNPs to PCM. Groups were admixture matched with no difference observed in population ancestry inference, indicating that the absence of association between CTLA-4 polymorphisms and PCM could not be attributed to ancestral bias. This study showed that there was no association between the CTLA-4 SNPs -318 and +49 and the resistance or susceptibility to PCM. |
description |
The CTLA-4 protein is expressed in activated T cells and plays an essential role in the immune response through its regulatory effect on T cell activation. Polymorphisms of the CTLA-4 gene have been correlated with autoimmune, neoplastic and infectious illnesses. This work aimed to verify possible associations between single nucleotide polymorphisms (SNPs) in CTLA-4, -318C/T in the promoter and +49A/G in exon 1 and paracoccidioidomycosis (PCM) caused by Paracoccidioides brasiliensis. For this purpose, 66 chronic form PCM patients and 76 healthy controls had their allele, genotype and haplotype frequencies determined. The genetic admixture structure of the patients and controls was evaluated to eliminate ancestral bias. The comparison of frequencies indicated no significant differences between patients and controls that could link the SNPs to PCM. Groups were admixture matched with no difference observed in population ancestry inference, indicating that the absence of association between CTLA-4 polymorphisms and PCM could not be attributed to ancestral bias. This study showed that there was no association between the CTLA-4 SNPs -318 and +49 and the resistance or susceptibility to PCM. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-03-01 |
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://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762011000200017 |
url |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762011000200017 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0074-02762011000200017 |
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 |
Instituto Oswaldo Cruz, Ministério da Saúde |
publisher.none.fl_str_mv |
Instituto Oswaldo Cruz, Ministério da Saúde |
dc.source.none.fl_str_mv |
Memórias do Instituto Oswaldo Cruz v.106 n.2 2011 reponame:Memórias do Instituto Oswaldo Cruz instname:Fundação Oswaldo Cruz instacron:FIOCRUZ |
reponame_str |
Memórias do Instituto Oswaldo Cruz |
collection |
Memórias do Instituto Oswaldo Cruz |
instname_str |
Fundação Oswaldo Cruz |
instacron_str |
FIOCRUZ |
institution |
FIOCRUZ |
repository.name.fl_str_mv |
Memórias do Instituto Oswaldo Cruz - Fundação Oswaldo Cruz |
repository.mail.fl_str_mv |
|
_version_ |
1669937708919685120 |