自身免疫性溶血性贫血的现状

Q4 Medicine
P. Vasilchenkova, I. Galtseva, E. Lukina
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引用次数: 0

摘要

自身免疫性溶血性贫血是一种罕见的疾病,其特征是出现抗红细胞自身抗体,随后免疫系统细胞破坏红细胞。携带自身抗体的红细胞的破坏机制已得到很好的研究;然而,触发自身红细胞抗原抗体产生的初始机制尚不清楚。在自身免疫性溶血性贫血的发病机制中,免疫耐受受损起着重要作用,其中t淋巴细胞起着关键作用。利用流式细胞术研究自身免疫性溶血性贫血患者的t淋巴细胞亚群,可以为研究自身免疫性溶血性贫血的发病机制和开发新的治疗方法提供有价值的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Autoimmune hemolytic anemia: the current state of the issue
Autoimmune hemolytic anemia is a rare disease characterized by the appearance of anti-erythrocyte autoantibodies and subsequent destruction of red blood cells by cells of the immune system. The destruction mechanisms of erythrocytes loaded with autoantibodies are well studied; however, the initial mechanisms that trigger the production of antibodies to own erythrocytes antigens remain unclear. In the pathogenesis of autoimmune hemolytic anemia, an important role is played by impaired immunological tolerance, in which T-lymphocytes play a key role. The study of T-lymphocytes subpopulation in patients with autoimmune hemolytic anemia by flow cytometry can provide valuable information for studying the disease pathogenesis and developing new approaches to its treatment.
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
20
审稿时长
12 weeks
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