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免疫性血小板减少症患者血浆蛋白质组学的可行性

Feasibility of plasma proteomics in patients with immune thrombocytopenia.

作者信息

Kapur Rick

机构信息

Sanquin Research, Department of Experimental Immunohematology, Amsterdam and Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Br J Haematol. 2025 Jan;206(1):394-396. doi: 10.1111/bjh.19882. Epub 2024 Nov 5.

Abstract

ITP is an acquired autoimmune bleeding disorder characterized by an isolated thrombocytopenia. The pathophysiology is highly multifactorial and involves antibody- and/or cytotoxic T cell-mediated killing of platelets and disruption of megakaryocyte function hampering platelet production. ITP remains a diagnosis of exclusion, and due to the high degree of variability between patients, it remains challenging to predict disease courses and responses to therapeutic agents. Hence, diagnostic and therapeutic laboratory biomarkers are highly warranted. To address this issue, in their paper, Jiang and colleagues have performed plasma proteomics in ITP patients (n = 40), in comparison to patients with thrombocytopenia due to other causes than ITP (non-ITP thrombocytopenia, n = 19) and healthy controls (n = 18). The data underscore that patients with ITP have a distinct plasma proteomic signature compared to non-ITP thrombocytopenia patients and healthy individuals. The findings should be further validated and investigated but suggest that the application of plasma proteomics is feasible and promising with respect to the search for potential biomarkers in patients with ITP. Commentary on: Jiang et al. Targeted proteomics profiling reveals valuable biomarkers in the diagnosis of primary immune thrombocytopenia. Br J Haematol 2025; 206:133-143.

摘要

免疫性血小板减少症(ITP)是一种获得性自身免疫性出血性疾病,其特征为孤立性血小板减少。其病理生理学具有高度多因素性,涉及抗体和/或细胞毒性T细胞介导的血小板杀伤以及巨核细胞功能破坏,从而阻碍血小板生成。ITP仍然是一种排除性诊断,并且由于患者之间存在高度变异性,预测疾病进程和对治疗药物的反应仍然具有挑战性。因此,非常有必要寻找诊断和治疗的实验室生物标志物。为了解决这个问题,Jiang及其同事在论文中对40例ITP患者、19例因ITP以外其他原因导致血小板减少的患者(非ITP血小板减少症)和18例健康对照进行了血浆蛋白质组学研究。数据强调,与非ITP血小板减少症患者和健康个体相比,ITP患者具有独特的血浆蛋白质组学特征。这些发现应进一步验证和研究,但表明血浆蛋白质组学在寻找ITP患者潜在生物标志物方面是可行且有前景的。对Jiang等人的评论:靶向蛋白质组学分析揭示了原发性免疫性血小板减少症诊断中的有价值生物标志物。《英国血液学杂志》2025年;206:133 - 143。

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