Non-classical human leucocyte antigens in ankylosing spondylitis

Detalhes bibliográficos
Autor(a) principal: Santos, Margarida Rodrigues
Data de Publicação: 2018
Outros Autores: Couto, Ana Rita, Foroni, Iris, Bettencourt, Bruno Filipe, Li, Zhixiu, Meneses, Raquel, Wheeler, Lawrie, Pereira, Joaquim, Pimentel-Santos, Fernando, Fonseca, João Eurico, Alves, Helena, Martinho, António, Lima, Manuela, Brown, Matthew A., Bruges-Armas, Jácome
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.1136/rmdopen-2018-000677
Resumo: Objectives Ankylosing spondylitis (AS) is the most prevalent form of spondyloarthritis, with a known genetic association with the HLA-B27 molecule. The aim of this study was to assess the contribution of the HLA-G, HLA-E and HLA-F to AS susceptibility/protection in Portuguese patients with HLA-B27 AS and HLA-B27 unaffected controls. Methods High-resolution typing of HLA-G, HLA - E and HLA - F was performed in 228 patients with HLA-B27 AS and 244 HLA-B27 unaffected controls. Allelic, genotypic and haplotypic frequencies were compared between cohorts. To replicate the results, single nucleotide polymorphisms (SNPs) in HLA-E and HLA-F genes were typed in Australian cohorts. For further confirmation, a group of European-descent patients with AS and unaffected controls were genotyped for Major Histocompatibility Complex SNPs using the Illumina microarray. Results In the Portuguese population, no significant differences were found in HLA-G. For HLA-E, a significant difference was detected for the genotype HLA-E∗01:01:01/01:03:01 (p=0.009; pc=0.009; OR=0.51), with a protection effect. For HLA-F, significant differences were detected in the allele HLA-F∗01:01:02 (p=0.0049; pc=0.0098; OR=0.60) and corresponding SNP rs2075682 (p=0.0004; pc=0.0008; OR=0.53), suggesting protection and in the genotype HLA-F∗01:01:01/01:03:01 (p=0.011; pc=0.043; OR=2.00), suggesting a susceptibility effect. Three G-E-F haplotypes with significant differences were detected but occur in a very small number of individuals. The only significant differences detected in the replication studies were for HLA-E rs1059510 in the Australians and for HLA-F rs1736924 in the European-descent cohorts. Conclusion Our results reveal suggestive AS protective and susceptibility effects from both HLA-E and HLA - F loci, however with population differences. To our knowledge, this is the first study showing association of HLA-F with AS.
id RCAP_8a9828a1a116da53bec81dbf622595bf
oai_identifier_str oai:run.unl.pt:10362/41963
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Non-classical human leucocyte antigens in ankylosing spondylitisPossible association with HLA-E and HLA-Fankylosing spondylitisautoimmune diseasesgene polymorphismHLAinflammationspondyloarthritisRheumatologyImmunology and AllergyImmunologyObjectives Ankylosing spondylitis (AS) is the most prevalent form of spondyloarthritis, with a known genetic association with the HLA-B27 molecule. The aim of this study was to assess the contribution of the HLA-G, HLA-E and HLA-F to AS susceptibility/protection in Portuguese patients with HLA-B27 AS and HLA-B27 unaffected controls. Methods High-resolution typing of HLA-G, HLA - E and HLA - F was performed in 228 patients with HLA-B27 AS and 244 HLA-B27 unaffected controls. Allelic, genotypic and haplotypic frequencies were compared between cohorts. To replicate the results, single nucleotide polymorphisms (SNPs) in HLA-E and HLA-F genes were typed in Australian cohorts. For further confirmation, a group of European-descent patients with AS and unaffected controls were genotyped for Major Histocompatibility Complex SNPs using the Illumina microarray. Results In the Portuguese population, no significant differences were found in HLA-G. For HLA-E, a significant difference was detected for the genotype HLA-E∗01:01:01/01:03:01 (p=0.009; pc=0.009; OR=0.51), with a protection effect. For HLA-F, significant differences were detected in the allele HLA-F∗01:01:02 (p=0.0049; pc=0.0098; OR=0.60) and corresponding SNP rs2075682 (p=0.0004; pc=0.0008; OR=0.53), suggesting protection and in the genotype HLA-F∗01:01:01/01:03:01 (p=0.011; pc=0.043; OR=2.00), suggesting a susceptibility effect. Three G-E-F haplotypes with significant differences were detected but occur in a very small number of individuals. The only significant differences detected in the replication studies were for HLA-E rs1059510 in the Australians and for HLA-F rs1736924 in the European-descent cohorts. Conclusion Our results reveal suggestive AS protective and susceptibility effects from both HLA-E and HLA - F loci, however with population differences. To our knowledge, this is the first study showing association of HLA-F with AS.NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)Centro de Estudos de Doenças Crónicas (CEDOC)RUNSantos, Margarida RodriguesCouto, Ana RitaForoni, IrisBettencourt, Bruno FilipeLi, ZhixiuMeneses, RaquelWheeler, LawriePereira, JoaquimPimentel-Santos, FernandoFonseca, João EuricoAlves, HelenaMartinho, AntónioLima, ManuelaBrown, Matthew A.Bruges-Armas, Jácome2018-07-18T22:16:30Z2018-06-012018-06-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.1136/rmdopen-2018-000677eng2044-6055PURE: 5477315http://www.scopus.com/inward/record.url?scp=85049483719&partnerID=8YFLogxKhttps://doi.org/10.1136/rmdopen-2018-000677info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T04:22:39Zoai:run.unl.pt:10362/41963Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:31:25.710919Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Non-classical human leucocyte antigens in ankylosing spondylitis
Possible association with HLA-E and HLA-F
title Non-classical human leucocyte antigens in ankylosing spondylitis
spellingShingle Non-classical human leucocyte antigens in ankylosing spondylitis
Santos, Margarida Rodrigues
ankylosing spondylitis
autoimmune diseases
gene polymorphism
HLA
inflammation
spondyloarthritis
Rheumatology
Immunology and Allergy
Immunology
title_short Non-classical human leucocyte antigens in ankylosing spondylitis
title_full Non-classical human leucocyte antigens in ankylosing spondylitis
title_fullStr Non-classical human leucocyte antigens in ankylosing spondylitis
title_full_unstemmed Non-classical human leucocyte antigens in ankylosing spondylitis
title_sort Non-classical human leucocyte antigens in ankylosing spondylitis
author Santos, Margarida Rodrigues
author_facet Santos, Margarida Rodrigues
Couto, Ana Rita
Foroni, Iris
Bettencourt, Bruno Filipe
Li, Zhixiu
Meneses, Raquel
Wheeler, Lawrie
Pereira, Joaquim
Pimentel-Santos, Fernando
Fonseca, João Eurico
Alves, Helena
Martinho, António
Lima, Manuela
Brown, Matthew A.
Bruges-Armas, Jácome
author_role author
author2 Couto, Ana Rita
Foroni, Iris
Bettencourt, Bruno Filipe
Li, Zhixiu
Meneses, Raquel
Wheeler, Lawrie
Pereira, Joaquim
Pimentel-Santos, Fernando
Fonseca, João Eurico
Alves, Helena
Martinho, António
Lima, Manuela
Brown, Matthew A.
Bruges-Armas, Jácome
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)
Centro de Estudos de Doenças Crónicas (CEDOC)
RUN
dc.contributor.author.fl_str_mv Santos, Margarida Rodrigues
Couto, Ana Rita
Foroni, Iris
Bettencourt, Bruno Filipe
Li, Zhixiu
Meneses, Raquel
Wheeler, Lawrie
Pereira, Joaquim
Pimentel-Santos, Fernando
Fonseca, João Eurico
Alves, Helena
Martinho, António
Lima, Manuela
Brown, Matthew A.
Bruges-Armas, Jácome
dc.subject.por.fl_str_mv ankylosing spondylitis
autoimmune diseases
gene polymorphism
HLA
inflammation
spondyloarthritis
Rheumatology
Immunology and Allergy
Immunology
topic ankylosing spondylitis
autoimmune diseases
gene polymorphism
HLA
inflammation
spondyloarthritis
Rheumatology
Immunology and Allergy
Immunology
description Objectives Ankylosing spondylitis (AS) is the most prevalent form of spondyloarthritis, with a known genetic association with the HLA-B27 molecule. The aim of this study was to assess the contribution of the HLA-G, HLA-E and HLA-F to AS susceptibility/protection in Portuguese patients with HLA-B27 AS and HLA-B27 unaffected controls. Methods High-resolution typing of HLA-G, HLA - E and HLA - F was performed in 228 patients with HLA-B27 AS and 244 HLA-B27 unaffected controls. Allelic, genotypic and haplotypic frequencies were compared between cohorts. To replicate the results, single nucleotide polymorphisms (SNPs) in HLA-E and HLA-F genes were typed in Australian cohorts. For further confirmation, a group of European-descent patients with AS and unaffected controls were genotyped for Major Histocompatibility Complex SNPs using the Illumina microarray. Results In the Portuguese population, no significant differences were found in HLA-G. For HLA-E, a significant difference was detected for the genotype HLA-E∗01:01:01/01:03:01 (p=0.009; pc=0.009; OR=0.51), with a protection effect. For HLA-F, significant differences were detected in the allele HLA-F∗01:01:02 (p=0.0049; pc=0.0098; OR=0.60) and corresponding SNP rs2075682 (p=0.0004; pc=0.0008; OR=0.53), suggesting protection and in the genotype HLA-F∗01:01:01/01:03:01 (p=0.011; pc=0.043; OR=2.00), suggesting a susceptibility effect. Three G-E-F haplotypes with significant differences were detected but occur in a very small number of individuals. The only significant differences detected in the replication studies were for HLA-E rs1059510 in the Australians and for HLA-F rs1736924 in the European-descent cohorts. Conclusion Our results reveal suggestive AS protective and susceptibility effects from both HLA-E and HLA - F loci, however with population differences. To our knowledge, this is the first study showing association of HLA-F with AS.
publishDate 2018
dc.date.none.fl_str_mv 2018-07-18T22:16:30Z
2018-06-01
2018-06-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://doi.org/10.1136/rmdopen-2018-000677
url https://doi.org/10.1136/rmdopen-2018-000677
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 2044-6055
PURE: 5477315
http://www.scopus.com/inward/record.url?scp=85049483719&partnerID=8YFLogxK
https://doi.org/10.1136/rmdopen-2018-000677
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799137937409966080