Association of Functional Polymorphisms of KIR3DL1/DS1 With Behcet's Disease

Behcet's disease (BD) is an immune-mediated vasculitis related to imbalances between the innate and adaptive immune response. Infectious agents or environmental factors may trigger the disease in genetically predisposed individuals. HLA-B51 is the genetic factor stronger associated with the dis...

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Detalles Bibliográficos
Autores: Castano-Nunez, Angel, Montes-Cano, Marco-Antonio, Garcia-Lozano, Jose-Raul, Ortego-Centeno, Norberto, Garcia-Hernandez, Francisco-Jose, Espinosa, Gerard, Grana-Gil, Genaro, Sanchez-Burson, Juan, Julia Benique, Maria Rosa, Solans, Roser, Blanco, Ricardo, Barnosi-Marin, Ana-Celia, Gomez de la Torre, Ricardo, Fanlo Mateo, Patricia, Rodriguez-Carballeira, Monica, Rodriguez-Rodriguez, Luis, Camps, Teresa, Castaneda, Santos, Alegre-Sancho, Juan-Jose, Martin, Javier, Gonzalez-Escribano, Maria-Francisca
Tipo de recurso: artículo
Fecha de publicación:2019
País:España
Institución:Instituto de Salud Carlos III (ISCIII)
Repositorio:Repisalud
Idioma:inglés
OAI Identifier:oai:repisalud.isciii.es:20.500.12105/22720
Acceso en línea:https://hdl.handle.net/20.500.12105/22720
Access Level:acceso abierto
Palabra clave:Behcet's disease
HLA
KIR
NK cells
Functional polymorphisms
Oportunidad Relativa
Predisposición Genética a la Enfermedad
Antígenos HLA
Femenino
Masculino
Alelos
Humanos
Frecuencia de los Genes
Estudios de Asociación Genética
Genotipo
Receptores KIR
Síndrome de Behçet
Polimorfismo Genético
Receptores KIR3DL1
Genetic Predisposition to Disease
Genotype
Behcet Syndrome
Alleles
Gene Frequency
Humans
HLA Antigens
Male
Female
Receptors, KIR3DL1
Receptors, KIR
Odds Ratio
Genetic Association Studies
Polymorphism, Genetic
Descripción
Sumario:Behcet's disease (BD) is an immune-mediated vasculitis related to imbalances between the innate and adaptive immune response. Infectious agents or environmental factors may trigger the disease in genetically predisposed individuals. HLA-B51 is the genetic factor stronger associated with the disease, although the bases of this association remain elusive. NK cells have also been implicated in the etiopathogenesis of BD. A family of NK receptors, Killer-cell Immunoglobulin-like Receptor (KIR), with a very complex organization, is very important in the education and control of the NK cells by the union to their ligands, most of them, HLA class I molecules. This study aimed to investigate the contribution of certain KIR functional polymorphisms to the susceptibility to BD. A total of 466 BD patients and 444 healthy individuals were genotyped in HLA class I (A, B, and C). The set of KIR genes and the functional variants of KIR3DL1/DS1 and KIR2DS4 were also determined. Frequency of KIR3DL1*004 was lower in patients than in controls (0.15 vs. 0.20, P = 0.005, Pc = 0.015; OR = 0.70; 95% CI 0.54-0.90) in both B51 positive and negative individuals. KIR3DL1*004, which encodes a misfolded protein, is included in a common telomeric haplotype with only one functional KIR gene, KIR3DL2. Both, KIR3DL1 and KIR3DL2 sense pathogen-associated molecular patterns but they have different capacities to eliminate them. The education of the NK cells depending on the HLA, the balance of KIR3DL1/KIR3DL2 licensed NK cells and the different capacities of these receptors to eliminate pathogens could be involved in the etiopathogenesis of BD.