Особенности генетического полиморфизма HLA-антигенов при приобретенной апластической анемии у детей

This study presents the genetic polymorphism of HLA-antigens in acquired aplastic anemia (AAA) in 147 children (85 boys и 62 girls) aged 1 to 18 with. The control group is consisted of 1700 umbilical cord blood samples of healthy newborns. The genetic polymorphism of HLA was studied in groups of children with AAA, divided by gender and age. Our results revealed distinction in HLA-markers of predisposition and sustainability to AAA. Possible differences in factors of immunogenetic predisposition suggest different mechanisms involved in the development of the disease in different groups of children and reconsider the existing model of the pathogenesis of AAA.В статье представлены результаты исследования генетического полиморфизма HLA-антигенов при приобретенной апластической анемии (ПАА) у 147 детей в возрасте от 1 до 18 лет. Контрольная группа была представлена 1700 образцами пуповинной крови условно здоровых новорожденных детей. Анализ полученных данных позволил выявить отличающиеся у детей разного пола и возраста HLA-маркеры предрасположенности и протекции к ПАА. Вероятное различие в факторах иммуногенетической предрасположенности позволяет предположить участие разных механизмов в развитии заболевания у разных групп детей и по-новому рассматривать уже имеющиеся модели патогенеза ПАА

Immunogenetic markers of Crohn's disease in adults population of the Moscow region

Aim: to study immunogenetic markers of predisposition to the development and protection for Crohn's disease in adults population of the Moscow region. Material and methods. The study included 53 samples of peripheral blood of patients with Crohn's disease in the Moscow region. The control group was represented by 1,700 samples of umbilical cord blood is healthy newborns. Revealing HLA antigens at low level performed by SSO method on DynalRELI 48 processor. The results received with ambiguous interpretation was using PCR-SSP method (Ivitrogen). Results. Were found the positive and negative associations of groups of HLA alleles with clinical form, the course of Crohn's disease and response to steroid treatment, in particular revealed that, predisposition to the development for Crohn's disease in women and with sensitivity to steroid treatment in this disease associated allele group C*12, to the characteristic restricting markers such as Crohn's disease include the В 38 and A*11 markers nonrestricting, nonpenetrating noninflammatory type groups are alleles B*56 and C*14 and C*14 is also associated with the risk of Crohn's disease in men, characteristic markers of protection to the development of the disease crown with chronic relapsing and severe clinical course are DQB1*02 and DQB1*03, respectively. Conclusion. These results demonstrate the need for studies of gene polymorphism HLA-system, not only in relation to the disease in general, but in selected patients with clinical groups.</p