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Journal Technologies of Living Systems №1 for 2017 г.
Article in number:
Role of genetic disturbances in systemic lupus erythematosus
Authors:
L.V. Ivanitskiy - Reumatologist, Moscow Regional Research Clinical Institute named after M.F.Vladimirskiy
E-mail: l.iwanitskiy@gmail.com
E.V. Smirnova - Post-graduate Student, Faculty of Fundamental Medicine, Department of Internal Medicine, Lomonosov Moscow State University
E-mail: elena.smirnova881@gmail.com
T.N. Krasnova - Ph.D. (Med.), Associate Professor, Faculty of Fundamental Medicine, Department of Internal Medicine, Lomonosov Moscow State University
E-mail: krasnovamgu@yandex.ru
L.M. Samokhodskaya - Ph.D. (Med.), Associate Professor, Medical Scientific Educational Centre of Lomonosov Moscow State University
E-mail: slm@fbm.msu.ru
Abstract:
Systemic lupus erythematosus (SLE) is an autoimmune systemic disease characterized by the autoantibodies formation and development of immune inflammation affecting many organs and systems. The clinical symptoms, different prognosis and course of the disease probably are related to the predominant pathogenic type of disturbances. Pathogenesis of systemic lesions in SLE has several major areas - cytotoxic, immunologic and thrombotic with the subsequent development of inflammatory reactions. Genetic disorders in the pathogenesis of SLE are discussed for decades. According to the GWAS reports in different populations there are revealed different candidate genes associated with autoimmunity disorders. Great importance among genetic factors in the development of SLE genes belongs to molecules of histocompatibility complex class II and III (MHC II and III), Fc receptors, cytokines and disturbances of neutrophil function. These studies are discussed in the article suggest that the development and clinical variability SLE are largely associated with genetic disorders. Individual assessment of gene polymorphic variants will allow a personalized approach to the management and treatment of patients with SLE and choose the most appropriate therapy based on the predisposition to a particular clinical course of the disease.
Pages: 18-24
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