The importance of specific autoimmune disorders in the pathogenesis of psoriasis and the prospects of immunobiological therapy of dermatosis

K. S. Tkachyshyna
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Abstract

Objective — to analyze the features of specific autoimmune disorders in patients with psoriasis, determine their importance in the pathogenesis of this dermatosis, and assess the prospects of immunobiological therapy for dermatosis. Materials and methods. Based on an in-depth analysis of the results of modern special studies, the leading role of specific autoantigens and autoantibodies in the body of patients with this dermatosis has been confirmed in the pathogenesis of psoriasis. Results and discussion. The article analyzes the importance of specific autoantigens, including keratin-17, LL-37, ADAMTSL5, and lipid antigens generated by PLA2G4D, which are essential in the pathogenesis of psoriasis. Emphasis is placed on the potential importance of immunobiological therapy, which significantly decrease levels of autoantigens LL-37 and ADAMTSL5 in areas of skin affected by psoriatic rash. The prospects of therapeutic approaches to the inhibition of cytokines derived from T cells and innate cells, such as IL-17, as well as to the inhibition of PLA2G4D or CD1a are also considered. Further study of specific autoimmune disorders in patients with psoriasis is important to improve therapeutic approaches to the treatment of psoriasis. Conclusions. Autoimmune disorders, combined with genetic and a number of other factors, are one of the important of the development of psoriasis. Analysis of the results of current special studies has promising therapeutic value because, in addition to supporting approaches to inhibiting cytokines derived from T cells and dendritic cells, they support the development of approaches to inhibiting autoantigens directly.
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特异性自身免疫性疾病在牛皮癣发病机制中的重要性及皮肤病免疫生物学治疗的前景
目的:分析牛皮癣患者特异性自身免疫性疾病的特点,确定其在牛皮癣发病机制中的重要性,并评估免疫生物学治疗牛皮癣的前景。材料和方法。基于对现代特殊研究结果的深入分析,已经证实了这种皮肤病患者体内特异性自身抗原和自身抗体在牛皮癣发病机制中的主导作用。结果和讨论。本文分析了特异性自身抗原的重要性,包括角蛋白-17、LL-37、ADAMTSL5和PLA2G4D产生的脂质抗原,这些抗原在银屑病的发病过程中至关重要。重点放在免疫生物学治疗的潜在重要性上,免疫生物学治疗可以显著降低银屑病皮疹影响皮肤区域的自身抗原LL-37和ADAMTSL5的水平。本文还考虑了抑制来自T细胞和先天细胞(如IL-17)的细胞因子以及抑制PLA2G4D或CD1a的治疗方法的前景。进一步研究银屑病患者的特异性自身免疫性疾病对改善银屑病的治疗方法具有重要意义。结论。自身免疫性疾病,结合遗传和许多其他因素,是银屑病发展的重要因素之一。对当前特殊研究结果的分析具有很好的治疗价值,因为除了支持抑制来自T细胞和树突状细胞的细胞因子的方法外,它们还支持直接抑制自身抗原的方法的发展。
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