自身免疫性溶血性贫血(AIHA)患者有核红细胞超微结构分析。

IF 1.1 4区 医学 Q4 MICROSCOPY Ultrastructural Pathology Pub Date : 2023-07-04 DOI:10.1080/01913123.2023.2211358
Jing Liu, Shuxu Dong, Yongxin Ru
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引用次数: 0

摘要

自身免疫性溶血性贫血(AIHA)是一组以免疫介导的成熟红细胞(rbc)溶解为特征的疾病。根据自身抗体产生的病因和机制,主要分为原发性和继发性。AIHA的诊断采用光镜下骨髓涂片形态学观察和单特异性直接抗球蛋白试验检测溶血。在这里,我们回顾性地用透射电镜观察了10例AIHA患者骨髓中有核红细胞的超微结构异常。结果显示有核红细胞受到严重的损伤,包括形态不规则、固缩、核溶解、核周池扩大和细胞质溶解。这些结果表明,异常免疫不仅攻击成熟红细胞,而且攻击有核红细胞,造血功能低下是AIHA发病的部分原因。
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Ultrastructural analysis of nucleated erythrocyte in patients with autoimmune hemolytic anemia (AIHA).

Autoimmune hemolytic anemia (AIHA) is a group of diseases characterized by immune-mediated lysis of mature red blood cells (RBCs). It is mainly classified into primary and secondary types based on etiology and mechanisms underlying autoantibody production. AIHA is diagnosed using morphological observation of bone marrow smears under a light microscope and monospecific direct antiglobulin test to detect hemolysis. Here, we retrospectively studied ultrastructural abnormalities of nucleated erythroid cells in bone marrows from 10 patients with AIHA using transmission electron microscopy. Our results revealed severe damage and injury to nucleated erythroid cells, including morphological irregularity, pyknosis, karyolysis, expansion of perinuclear cisternae and cytoplasmic lysis. These results indicate that aberrant immunity attacks not only mature RBCs but also nucleated erythroid cells, and ineffective hematopoiesis is partly involved in the pathogenesis of AIHA.

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来源期刊
Ultrastructural Pathology
Ultrastructural Pathology 医学-病理学
CiteScore
2.00
自引率
10.00%
发文量
40
审稿时长
6-12 weeks
期刊介绍: Ultrastructural Pathology is the official journal of the Society for Ultrastructural Pathology. Published bimonthly, we are the only journal to be devoted entirely to diagnostic ultrastructural pathology. Ultrastructural Pathology is the ideal journal to publish high-quality research on the following topics: Advances in the uses of electron microscopic and immunohistochemical techniques Correlations of ultrastructural data with light microscopy, histochemistry, immunohistochemistry, biochemistry, cell and tissue culturing, and electron probe analysis Important new, investigative, clinical, and diagnostic EM methods.
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