Polymorphisms in the TGFB1 and IL2RA genes are associated with clinical forms of leprosy in Brazilian population

Detalhes bibliográficos
Autor(a) principal: Camargo, Rodrigo Mendes de [UNESP]
Data de Publicação: 2018
Outros Autores: Silva, Weber Laurentino da [UNESP], Medeiros, Priscila [UNESP], Fernandes Belone, Andrea de Faria, Pereira Latini, Ana Carla [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/0074-02760180274
http://hdl.handle.net/11449/185194
Resumo: BACKGROUND Leprosy is a chronic infectious disease caused by Mycobacterium leprae, and compromises the skin and peripheral nerves. This disease has been classified as multibacillary (MB) or paucibacillary (PB) depending on the host immune response. Genetic epidemiology studies in leprosy have shown the influence of human genetic components on the disease outcomes. OBJECTIVES We conducted an association study for IL2RA and TGFBI genes with clinical forms of leprosy based on two case-control samples. These genes encode important molecules for the immunosuppressive activity of Treg cells and present differential expressions according to the clinical forms of leprosy. Furthermore, IL2RA is a positional candidate gene because it is located near the 10p13 chromosome region, presenting a linkage peak for PB leprosy. METHODS A total of 885 leprosy cases were included in the study; 406 cases from Rondonopolis County (start population), a hyperendemic region for leprosy in Brazil, and 479 cases from Sao Paulo state (replication population), which has lower epidemiological indexes for the disease. We tested 11 polymorphisms in the IL2RA gene and the missense variant rs1800470 in the TGFB1 gene. FINDINGS The AA genotype of rs2386841 in IL2RA was associated with the PB form in the start population. The AA genotype of rs1800470 in TGFBI was associated with the MB form in the start population, and this association was confirmed for the replication population. MAIN CONCLUSIONS We demonstrated, for the first time, an association data with the PB form for a gene located on chromosome 10. In addition, we reported the association of TGFBI gene with the MB form. Our results place these genes as candidates for validation and replication studies in leprosy polarisation.
id UNSP_4d4c5973f11589f27e0fe7a9616160b8
oai_identifier_str oai:repositorio.unesp.br:11449/185194
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Polymorphisms in the TGFB1 and IL2RA genes are associated with clinical forms of leprosy in Brazilian populationleprosygenetic epidemiologyTGFB1IL2RATregsBACKGROUND Leprosy is a chronic infectious disease caused by Mycobacterium leprae, and compromises the skin and peripheral nerves. This disease has been classified as multibacillary (MB) or paucibacillary (PB) depending on the host immune response. Genetic epidemiology studies in leprosy have shown the influence of human genetic components on the disease outcomes. OBJECTIVES We conducted an association study for IL2RA and TGFBI genes with clinical forms of leprosy based on two case-control samples. These genes encode important molecules for the immunosuppressive activity of Treg cells and present differential expressions according to the clinical forms of leprosy. Furthermore, IL2RA is a positional candidate gene because it is located near the 10p13 chromosome region, presenting a linkage peak for PB leprosy. METHODS A total of 885 leprosy cases were included in the study; 406 cases from Rondonopolis County (start population), a hyperendemic region for leprosy in Brazil, and 479 cases from Sao Paulo state (replication population), which has lower epidemiological indexes for the disease. We tested 11 polymorphisms in the IL2RA gene and the missense variant rs1800470 in the TGFB1 gene. FINDINGS The AA genotype of rs2386841 in IL2RA was associated with the PB form in the start population. The AA genotype of rs1800470 in TGFBI was associated with the MB form in the start population, and this association was confirmed for the replication population. MAIN CONCLUSIONS We demonstrated, for the first time, an association data with the PB form for a gene located on chromosome 10. In addition, we reported the association of TGFBI gene with the MB form. Our results place these genes as candidates for validation and replication studies in leprosy polarisation.Inst Lauro de Souza Lima, Bauru, SP, BrazilUniv Estadual Paulista, Fac Med Botucatu, Dept Doencas Tropicais & Diagnost Imagem, Botucatu, SP, BrazilUniv Estadual Paulista, Fac Med Botucatu, Dept Doencas Tropicais & Diagnost Imagem, Botucatu, SP, BrazilFundaco Oswaldo CruzInst Lauro de Souza LimaUniversidade Estadual Paulista (Unesp)Camargo, Rodrigo Mendes de [UNESP]Silva, Weber Laurentino da [UNESP]Medeiros, Priscila [UNESP]Fernandes Belone, Andrea de FariaPereira Latini, Ana Carla [UNESP]2019-10-04T12:33:27Z2019-10-04T12:33:27Z2018-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article7application/pdfhttp://dx.doi.org/10.1590/0074-02760180274Memorias Do Instituto Oswaldo Cruz. Rio De Janeiro, Rj: Fundaco Oswaldo Cruz, v. 113, n. 12, 7 p., 2018.0074-0276http://hdl.handle.net/11449/18519410.1590/0074-02760180274S0074-02762018001200304WOS:000452627300001S0074-02762018001200304.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMemorias Do Instituto Oswaldo Cruzinfo:eu-repo/semantics/openAccess2023-12-13T06:16:30Zoai:repositorio.unesp.br:11449/185194Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-12-13T06:16:30Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Polymorphisms in the TGFB1 and IL2RA genes are associated with clinical forms of leprosy in Brazilian population
title Polymorphisms in the TGFB1 and IL2RA genes are associated with clinical forms of leprosy in Brazilian population
spellingShingle Polymorphisms in the TGFB1 and IL2RA genes are associated with clinical forms of leprosy in Brazilian population
Camargo, Rodrigo Mendes de [UNESP]
leprosy
genetic epidemiology
TGFB1
IL2RA
Tregs
title_short Polymorphisms in the TGFB1 and IL2RA genes are associated with clinical forms of leprosy in Brazilian population
title_full Polymorphisms in the TGFB1 and IL2RA genes are associated with clinical forms of leprosy in Brazilian population
title_fullStr Polymorphisms in the TGFB1 and IL2RA genes are associated with clinical forms of leprosy in Brazilian population
title_full_unstemmed Polymorphisms in the TGFB1 and IL2RA genes are associated with clinical forms of leprosy in Brazilian population
title_sort Polymorphisms in the TGFB1 and IL2RA genes are associated with clinical forms of leprosy in Brazilian population
author Camargo, Rodrigo Mendes de [UNESP]
author_facet Camargo, Rodrigo Mendes de [UNESP]
Silva, Weber Laurentino da [UNESP]
Medeiros, Priscila [UNESP]
Fernandes Belone, Andrea de Faria
Pereira Latini, Ana Carla [UNESP]
author_role author
author2 Silva, Weber Laurentino da [UNESP]
Medeiros, Priscila [UNESP]
Fernandes Belone, Andrea de Faria
Pereira Latini, Ana Carla [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Inst Lauro de Souza Lima
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Camargo, Rodrigo Mendes de [UNESP]
Silva, Weber Laurentino da [UNESP]
Medeiros, Priscila [UNESP]
Fernandes Belone, Andrea de Faria
Pereira Latini, Ana Carla [UNESP]
dc.subject.por.fl_str_mv leprosy
genetic epidemiology
TGFB1
IL2RA
Tregs
topic leprosy
genetic epidemiology
TGFB1
IL2RA
Tregs
description BACKGROUND Leprosy is a chronic infectious disease caused by Mycobacterium leprae, and compromises the skin and peripheral nerves. This disease has been classified as multibacillary (MB) or paucibacillary (PB) depending on the host immune response. Genetic epidemiology studies in leprosy have shown the influence of human genetic components on the disease outcomes. OBJECTIVES We conducted an association study for IL2RA and TGFBI genes with clinical forms of leprosy based on two case-control samples. These genes encode important molecules for the immunosuppressive activity of Treg cells and present differential expressions according to the clinical forms of leprosy. Furthermore, IL2RA is a positional candidate gene because it is located near the 10p13 chromosome region, presenting a linkage peak for PB leprosy. METHODS A total of 885 leprosy cases were included in the study; 406 cases from Rondonopolis County (start population), a hyperendemic region for leprosy in Brazil, and 479 cases from Sao Paulo state (replication population), which has lower epidemiological indexes for the disease. We tested 11 polymorphisms in the IL2RA gene and the missense variant rs1800470 in the TGFB1 gene. FINDINGS The AA genotype of rs2386841 in IL2RA was associated with the PB form in the start population. The AA genotype of rs1800470 in TGFBI was associated with the MB form in the start population, and this association was confirmed for the replication population. MAIN CONCLUSIONS We demonstrated, for the first time, an association data with the PB form for a gene located on chromosome 10. In addition, we reported the association of TGFBI gene with the MB form. Our results place these genes as candidates for validation and replication studies in leprosy polarisation.
publishDate 2018
dc.date.none.fl_str_mv 2018-01-01
2019-10-04T12:33:27Z
2019-10-04T12:33:27Z
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 http://dx.doi.org/10.1590/0074-02760180274
Memorias Do Instituto Oswaldo Cruz. Rio De Janeiro, Rj: Fundaco Oswaldo Cruz, v. 113, n. 12, 7 p., 2018.
0074-0276
http://hdl.handle.net/11449/185194
10.1590/0074-02760180274
S0074-02762018001200304
WOS:000452627300001
S0074-02762018001200304.pdf
url http://dx.doi.org/10.1590/0074-02760180274
http://hdl.handle.net/11449/185194
identifier_str_mv Memorias Do Instituto Oswaldo Cruz. Rio De Janeiro, Rj: Fundaco Oswaldo Cruz, v. 113, n. 12, 7 p., 2018.
0074-0276
10.1590/0074-02760180274
S0074-02762018001200304
WOS:000452627300001
S0074-02762018001200304.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Memorias Do Instituto Oswaldo Cruz
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 7
application/pdf
dc.publisher.none.fl_str_mv Fundaco Oswaldo Cruz
publisher.none.fl_str_mv Fundaco Oswaldo Cruz
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1803046924616466432