原发性与继发性免疫性血小板减少症(ITP):2023年麦克马斯特ITP峰会会议报告
Primary versus Secondary Immune Thrombocytopenia (ITP): A Meeting Report from the 2023 McMaster ITP Summit.
作者信息
Modi Dimpy, Chowdhury Saifur R, Mahamad Syed, Modi Hayley, Cines Douglas B, Neunert Cindy E, Al-Samkari Hanny, Cooper Nichola, Moulis Guillaume, Cunningham-Rundles Charlotte, Liebman Howard A, Bussel James B, Breakey Vicky R, Nazy Ishac, Arnold Donald M
机构信息
Michael G. DeGroote Centre for Transfusion Research, McMaster University, Hamilton, Ontario, Canada.
Health Research Methods, Evidence & Impact, McMaster University, Hamilton, Ontario, Canada.
出版信息
Thromb Haemost. 2025 Sep;125(9):923-932. doi: 10.1055/a-2508-1112. Epub 2024 Dec 24.
The McMaster Immune Thrombocytopenia (ITP) Summit, held on October 27, 2023, was an educational seminar from leading experts in immune thrombocytopenia and related disorders geared toward hematologists, internists, immunologists, and clinical and translational scientists. The focus of the Summit was to review the mechanisms, diagnosis, and treatment of primary versus secondary ITP. Specific objectives were to describe the unique features of secondary ITP, and to review its mechanisms in the context of autoimmune disease and infection. The key messages in this Summit were: (1) ITP is a heterogeneous disease, and genetic and immunologic insights may help classify patient subtypes; (2) exploring the autoimmune mechanisms and their association with hypogammaglobulinemia in patients with secondary ITP could improve our understanding of ITP and its subtypes; (3) investigating the mechanisms of ITP in the context of infections caused by viruses such as CMV, HIV, dengue, and hepatitis C, or bacteria such as , or vaccinations could provide insight into the causes of ITP. A better understanding of secondary ITP could help elucidate the pathogenesis of ITP.
2023年10月27日举行的麦克马斯特免疫性血小板减少症(ITP)峰会是一场由免疫性血小板减少症及相关疾病领域的顶尖专家举办的教育研讨会,面向血液学家、内科医生、免疫学家以及临床和转化科学家。峰会的重点是回顾原发性与继发性ITP的发病机制、诊断和治疗。具体目标是描述继发性ITP的独特特征,并在自身免疫性疾病和感染的背景下回顾其发病机制。本次峰会的关键信息如下:(1)ITP是一种异质性疾病,遗传学和免疫学见解可能有助于对患者亚型进行分类;(2)探索继发性ITP患者的自身免疫机制及其与低丙种球蛋白血症的关联,有助于我们更好地理解ITP及其亚型;(3)研究ITP在由巨细胞病毒、艾滋病毒、登革热和丙型肝炎等病毒或 等细菌引起的感染或疫苗接种背景下的发病机制,可能有助于深入了解ITP的病因。更好地理解继发性ITP有助于阐明ITP的发病机制。
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