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Association of TNFSF8 regulatory variants with excessive inflammatory responses but not leprosy per se.
Fava, Vinicius M; Cobat, Aurélie; Van Thuc, Nguyen; Latini, Ana Carla P; Stefani, Mariane M A; Belone, Andrea F; Ba, Nguyen Ngoc; Orlova, Marianna; Manry, Jérémy; Mira, Marcelo T; Thai, Vu Hong; Abel, Laurent; Alcaïs, Alexandre; Schurr, Erwin.
Afiliação
  • Fava VM; Program in Immunology and Infectious Diseases in Global Health, Research Institute of the McGill University Health Centre The McGill International TB Centre, Departments of Human Genetics and Medicine, McGill University, Montreal, Quebec, Canada.
  • Cobat A; Program in Immunology and Infectious Diseases in Global Health, Research Institute of the McGill University Health Centre The McGill International TB Centre, Departments of Human Genetics and Medicine, McGill University, Montreal, Quebec, Canada.
  • Van Thuc N; Hospital for Dermato-Venerology, Ho Chi Minh City, District 3, Vietnam.
  • Latini AC; Lauro de Souza Lima Institute, Bauru, São Paulo.
  • Stefani MM; Tropical Pathology and Public Health Institute, Federal University of Goiás, Goiânia.
  • Belone AF; Lauro de Souza Lima Institute, Bauru, São Paulo.
  • Ba NN; Hospital for Dermato-Venerology, Ho Chi Minh City, District 3, Vietnam.
  • Orlova M; The McGill International TB Centre, Departments of Human Genetics and Medicine, McGill University, Montreal, Quebec, Canada.
  • Manry J; Program in Immunology and Infectious Diseases in Global Health, Research Institute of the McGill University Health Centre The McGill International TB Centre, Departments of Human Genetics and Medicine, McGill University, Montreal, Quebec, Canada.
  • Mira MT; Core for Advanced Molecular Investigation, Pontifical Catholic University of Paraná, Curitiba, Brazil.
  • Thai VH; Hospital for Dermato-Venerology, Ho Chi Minh City, District 3, Vietnam.
  • Abel L; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Institut National de la Santé et de la Recherche Médicale University Paris Descartes, Imagine Institute St Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, New York.
  • Alcaïs A; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Institut National de la Santé et de la Recherche Médicale University Paris Descartes, Imagine Institute Centre d'Investigation Clinique, Unité de Recherche Clinique, Necker and Cochin Hospitals, Paris, France St Giles Laboratory of
  • Schurr E; Program in Immunology and Infectious Diseases in Global Health, Research Institute of the McGill University Health Centre The McGill International TB Centre, Departments of Human Genetics and Medicine, McGill University, Montreal, Quebec, Canada.
J Infect Dis ; 211(6): 968-77, 2015 Mar 15.
Article em En | MEDLINE | ID: mdl-25320285
ABSTRACT

BACKGROUND:

Type 1 reactions (T1R) affect a considerable proportion of patients with leprosy. In those with T1R, the host immune response pathologically overcompensates for the actual infectious threat, resulting in nerve damage and permanent disability. Based on the results of a genome-wide association study of leprosy per se, we investigated the TNFSF15 chromosomal region for a possible contribution to susceptibility to T1R.

METHODS:

We performed a high-resolution association scan of the TNFSF15 locus to evaluate the association with T1R in 2 geographically and ethnically distinct populations a family-based sample from Vietnam and a case-control sample from Brazil, comprising a total of 1768 subjects.

RESULTS:

In the Vietnamese sample, 47 single-nucleotide polymorphisms (SNPs) overlapping TNFSF15 and the adjacent TNFSF8 gene were associated with T1R but not with leprosy. Of the 47 SNPs, 39 were cis-expression quantitative trait loci (cis-eQTL) for TNFSF8 including SNPs located within the TNFSF15 gene. In the Brazilian sample, 18 of these cis-eQTL SNPs overlapping the TNFSF8 gene were validated for association with T1R.

CONCLUSIONS:

Taken together, these results indicate TNFSF8 and not TNFSF15 as an important T1R susceptibility gene. Our data support the need for infection genetics to go beyond genes for pathogen control to explore genes involved in a commensurate host response.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ligante CD30 / Hanseníase Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Infect Dis Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ligante CD30 / Hanseníase Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Infect Dis Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Canadá