association of 1661a/g cytotoxic t lymphocyte antigen-4 (ctla-4) gene polymorphism with a clinical subset of iranian children with systemic lupus erythematosus

نویسندگان

shirin farivar faculty of biological sciences, shahid beheshti university, general campus, tehran, ir iran; laser and plasma research institute, shahid beheshti university, general campus, tehran, ir iran; faculty of biological sciences, shahid beheshti university, general campus, tehran, ir iran. tel: +98-2129902733, fax: +98-2122431664

masoud dehghan tezerjani faculty of biological sciences, shahid beheshti university, general campus, tehran, ir iran

neda parvini faculty of biological sciences, shahid beheshti university, general campus, tehran, ir iran

reza shiari department of pediatrics, mofid children’s hospital, shahid beheshti university of medical sciences, tehran, ir iran; pediatrics infectious research center, shahid beheshti university of medical sciences, tehran, ir iran

چکیده

results our study showed that there were no statistically significant differences in the allele and genotype frequencies of -1661 a/g snp between patients with sle and healthy controls (p > 0.05). conclusions in conclusion, we found no association between snp-1661 a/g of the ctla-4 promoter region and susceptibility to sle in our population. objectives to evaluate the potential influences of common snp in ctla-4 promoter region (-1661 a/g), a case-control study was performed on iranian children. patients and methods genotypes of 31 patients and 50 healthy controls were investigated using the polymerase chain reaction-restriction fragment length polymorphism (pcr-rflp) method. background cytotoxic t-lymphocyte antigen-4 (ctla-4) is a molecule engaged in regulation of t cells. polymorphisms in the ctla-4 gene (ctla4) are known to be associated with several autoimmune diseases, including systemic lupus erythematosus.

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