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Polimorfismo +49 A/G del gen del antígeno 4 del linfocito T citotóxico (CTLA-4) en la diabetes tipo 1: Asociación con el perfil de anticuerpos y citoquinas / +49 A/G genetic polymorphism of cytotoxic T lymphocyte associated antigen 4 (CTLA-4) in type 7 diabetes: Association with autoantibodies and cytokines
Pérez B, Francisco; Codner D, Ethel; Ángel B, Bárbara; Balic N, Iván; Carrasco P, Elena.
  • Pérez B, Francisco; Universidad de Chile. Instituto de Nutrición y Tecnología de los Alimentos. Laboratorio de Epidemiología Nutricional. Santiago. CL
  • Codner D, Ethel; Universidad de Chile. Instituto de Investigaciones Materno Infantil. Santiago. CL
  • Ángel B, Bárbara; Universidad de Chile. Instituto de Nutrición y Tecnología de los Alimentos. Laboratorio de Epidemiología Nutricional. Santiago. CL
  • Balic N, Iván; Universidad de Chile. Instituto de Nutrición y Tecnología de los Alimentos. Laboratorio de Epidemiología Nutricional. Santiago. CL
  • Carrasco P, Elena; Hospital San Juan de Dios. Unidad de Diabetes. Santiago. CL
Rev. méd. Chile ; 137(3): 321-328, mar. 2009. ilus, tab
Article in Spanish | LILACS | ID: lil-518490
ABSTRACT
Background: Cytotoxic T lymphocyte associated antigen 4 (CTLA-4) has been one ofthe non HLA genes more commonly studied in type 1 diabetes mellitus (TID). CTLA-4 is a co-stimulation protein that has a key role in the negative regulation ofT cells and is related with a functional cytokine imbalance, generating a T helper (Th) 1 over Th2 dominance. Aim: To analyze the association of +49 A/G polymorphism of CTLA-4 and its relationship with autoantibodies and cytokine expression in recently diagnosed TID patients. Patients and Methods: CTLA-4 genetic variants and auto-antibody levéis were studied in 260 chiídren with TID and 255 healthy chiídren matched by age and gender +49 A/G polymorphism of CTLA-4 was studied by polymerase chain reaction and restriction fragmentpolymorphism (PCR-RFLP). Autoantibody levéis were measured by conventional ELISA. A panel of60 cytokines was studied simultaneously by serum array analysis in 15 TID and 15 healthy controls stratified according CTLA-4 genotype. Results: The +49 A/G genetic frequency was similar in TID cases and healthy chiídren. A positive anti-GAD65 and anti-IA-2 level was observed in 673 percent of TID group. This percentage was increased among GG carriers (79.4 percent to GAD65 and 70.6 percent to IA-2). Finally, TID patients carrying this genotype showed a high expression of interleukin 2, 10, tumor necrosis factor alpha and interferon gamma. Conclusions: The +49 A/G polymorphism of CTLA-4 was similar in diabetic and control chiídren. Among patients with TID and carriers of GG genotype, a higher frequency of anti-GAD65 and a preferential Thl cytokine expression profile was observed.
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Full text: Available Index: LILACS (Americas) Main subject: Polymorphism, Genetic / Autoantibodies / Antigens, CD / Cytokines / Diabetes Mellitus, Type 1 Type of study: Observational study / Risk factors Limits: Adolescent / Child / Female / Humans / Male Language: Spanish Journal: Rev. méd. Chile Journal subject: Medicine Year: 2009 Type: Article / Project document Affiliation country: Chile Institution/Affiliation country: Hospital San Juan de Dios/CL / Universidad de Chile/CL

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Full text: Available Index: LILACS (Americas) Main subject: Polymorphism, Genetic / Autoantibodies / Antigens, CD / Cytokines / Diabetes Mellitus, Type 1 Type of study: Observational study / Risk factors Limits: Adolescent / Child / Female / Humans / Male Language: Spanish Journal: Rev. méd. Chile Journal subject: Medicine Year: 2009 Type: Article / Project document Affiliation country: Chile Institution/Affiliation country: Hospital San Juan de Dios/CL / Universidad de Chile/CL