免疫性血小板减少性紫癜(ITP)患者CD44、CD90和CD96的表达。

Nadia ElMenshawy, Farha El-Chennawi, Ahmed Darwish, Asmaa Foda, Doaa Atita, Mohamed Eissa
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引用次数: 0

摘要

研究不同来源的造血干细胞标志物的表达可能有助于了解不同生态位条件下的干细胞生物学。该研究旨在评估造血干细胞在三种不同生态位条件下细胞表面标志物(CD44、CD90、CD96)的差异;脐带血(UCB),正常骨髓(NBM)和特发性(免疫性)血小板减少性紫癜(IBM)的骨髓样本。本研究对300例病例进行了研究,分为三个研究组;从妇产科剖宫产产妇采集脐带血100个单位,从大学儿童医院采集特发性(免疫性)血小板减少性紫癜患者骨髓100个单位,骨髓组织无疾病证据的正常骨髓100个单位。与IBM组相比,UCB组和NBM组CD44显著升高(
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CD44, CD90 and CD96 expression in immune thrombocytopenia purpura (ITP) patients.

Studying the expression of hematopoietic stem cell markers from different sources might be useful in understanding stem cell biology in different niche conditions. The study aimed to assess the difference in cell surface markers (CD44, CD90, CD96) on hematopoietic stem cells in three different niche conditions; umbilical cord blood (UCB), normal bone marrow (NBM) and bone marrow samples from idiopathic (immune) thrombocytopenic purpura (IBM). This study was conducted on 300 cases divided into three study groups; 100 umbilical cord blood units collected from mothers undergoing cesarian section in gynecology and obstetrics department, 100 bone marrow samples from idiopathic (immune) thrombocytopenic purpura patients collected from university children hospital and 100 normal bone marrow samples with no evidence of disease in bone marrow tissue. CD44 was significantly elevated in UCB and NBM groups compared to IBM group (<0.001). There was also a significant elevation of CD90 and CD96 in IBM group compared to NBM group and UCB (<0.001). CD90 and CD96 play a role in the pathogenesis of ITP disorder and could be applied as a targeted therapy to improve the outcome of this disease.

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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
38
审稿时长
>12 weeks
期刊介绍: The Journal of Immunoassay & Immunochemistry is an international forum for rapid dissemination of research results and methodologies dealing with all aspects of immunoassay and immunochemistry, as well as selected aspects of immunology. They include receptor assay, enzyme-linked immunosorbent assay (ELISA) in all of its embodiments, ligand-based assays, biological markers of ligand-receptor interaction, in vivo and in vitro diagnostic reagents and techniques, diagnosis of AIDS, point-of-care testing, clinical immunology, antibody isolation and purification, and others.
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