TY - JOUR
T1 - Estudio del polimorfismo de receptores Fcγlla en pacientes chilenos con lupus eritematoso sistémico
AU - Carrión A, Flavio
AU - Figueroa E, Fernando
AU - Martínez R, M. Eugenia
AU - Massardo V, Loreto
AU - Pérez G, Tamara
AU - Foster B, Carolina
AU - Mancilla M, Cecilia
AU - Neira Q, Oscar
AU - Guzmán B, Leonardo
AU - Valenzuela M, Viviana
AU - Urrutia L, Ramón
AU - Carmona G, Sergio
AU - Figueroa, Maximiliano
AU - Lubiano A, Alessandra
AU - Wainstein G, Eduardo
PY - 2003/1
Y1 - 2003/1
N2 - Background: Polymorphisms of Fc receptors for IgG (FcγR) have been proposed as a genetic factor that influences susceptibility for systemic lupus erythematosus (SLE). Human FćRIIa has 2 codominantly expressed alleles, H131 and R131, which differ at amino acid position 131 in the second extracelular domain (histidine or arginine respectively) and differ substantially in their ability to hind human IgG2. The H131 allele binds IgG2 efficiently, whereas R131 hinds it poorly. Because IgG2 is a poor activator of the classical complement pathway, the H131 is essential for the disposal of IgG2 immune complexes. Aim: To determine the distribution of FcγRIIA genes in a cohort of Chilean SLE patients, with or without a history of lupus nephritis. Patients and methods: We studied 52 Chilean SLE patients fulfilling the 1982 American College of Rheumatology (ACR) criteria, 20 of whom had a history of nephritis, and 44 ethnically matched disease-free controls. FcγRIIa allotypes were genotyped by PCR. Results: No significant association was observed between the low affinity FcγRII receptor (FcgRIIa-R131) and the presence of SLE or lupus nephritis. However, genotype frequencies in SLE patients but not in controls, departed from the proportions predicted by the Hardy-Weinberg equilibrium, suggesting this locus might be related to the disease. Conclusions: Our results suggest that in Chilean patients with SLE, as well as in many other populations, the R131 allotype is not a major factor predisposing to the development of SLE or lupus nephritis.
AB - Background: Polymorphisms of Fc receptors for IgG (FcγR) have been proposed as a genetic factor that influences susceptibility for systemic lupus erythematosus (SLE). Human FćRIIa has 2 codominantly expressed alleles, H131 and R131, which differ at amino acid position 131 in the second extracelular domain (histidine or arginine respectively) and differ substantially in their ability to hind human IgG2. The H131 allele binds IgG2 efficiently, whereas R131 hinds it poorly. Because IgG2 is a poor activator of the classical complement pathway, the H131 is essential for the disposal of IgG2 immune complexes. Aim: To determine the distribution of FcγRIIA genes in a cohort of Chilean SLE patients, with or without a history of lupus nephritis. Patients and methods: We studied 52 Chilean SLE patients fulfilling the 1982 American College of Rheumatology (ACR) criteria, 20 of whom had a history of nephritis, and 44 ethnically matched disease-free controls. FcγRIIa allotypes were genotyped by PCR. Results: No significant association was observed between the low affinity FcγRII receptor (FcgRIIa-R131) and the presence of SLE or lupus nephritis. However, genotype frequencies in SLE patients but not in controls, departed from the proportions predicted by the Hardy-Weinberg equilibrium, suggesting this locus might be related to the disease. Conclusions: Our results suggest that in Chilean patients with SLE, as well as in many other populations, the R131 allotype is not a major factor predisposing to the development of SLE or lupus nephritis.
KW - Lupus erythematosus, systemic
KW - Lupus nephritis
KW - Receptors, IgG
UR - http://www.scopus.com/inward/record.url?scp=0037945573&partnerID=8YFLogxK
M3 - Article
C2 - 12643213
AN - SCOPUS:0037945573
SN - 0034-9887
VL - 131
SP - 11
EP - 18
JO - Revista Medica de Chile
JF - Revista Medica de Chile
IS - 1
ER -