成人发病菊chi -藤本病单核细胞CD169表达升高

IF 0.9 Q4 HEMATOLOGY Hemato Pub Date : 2023-09-15 DOI:10.3390/hemato4030022
Giacomo Malipiero, Piernicola Machin, Anna Ermacora, Chiara Pratesi, Antonino Carbone, Desre’ Ethel Fontana, Kathreena Paul Vattamattathil, Rita De Rosa, Paolo Doretto
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引用次数: 0

摘要

Kikuchi-Fujimoto病(KFD)是一种罕见的良性淋巴增生性疾病,病因不明,可与其他炎性或克隆性淋巴增生性疾病相似。由于缺乏可用的血液生物标志物,诊断是基于受影响淋巴结的活检。近年来,越来越多的证据表明,失调的I型INF先天免疫反应在该疾病的发病机制中起着关键作用,可能是未来的治疗靶点。然而,测量干扰素α (INFα)和干扰素刺激基因(isg)表达的实验室检测方法繁琐且不广泛,限制了它们在临床和转化研究中的应用,并鼓励使用更方便的替代标记物。在这项研究中,快速流式细胞术检测了两名KFD患者循环单核细胞中CD169 (siglec1)的表达水平升高,这是一种由infα诱导的参与先天免疫调节的表面蛋白。我们的结果与以前的经验一致,并为更广泛地研究使用该检测方法探索KFD的病理生理学奠定了基础。
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Increased Expression of CD169 on Monocytes in Adult-Onset Kikuchi–Fujimoto Disease
Kikuchi–Fujimoto disease (KFD) is a rare, benign lymphoproliferative disease of uncertain origin that can mimic other inflammatory or clonal lymphoproliferative disorders. Given the lack of available blood biomarkers, diagnosis is based on the biopsy of an affected lymph node. In recent years, evidence has been mounting that a dysregulated type I INF innate immune response plays a pivotal role in the pathogenesis of the disease and might be a future therapeutic target. Nonetheless, laboratory assays measuring the expression of interferon alpha (INFα) and INF-stimulated genes (ISGs) are cumbersome and not widely available, limiting their use in clinical and translational research and encouraging the use of more convenient surrogate markers. In this study, a rapid flow cytometry assay detected increased levels of expression of CD169 (Siglec-1), an INFα-induced surface protein involved in innate immunity regulation, on circulating monocytes from two patients with KFD. Our results are in line with previous experiences and set the stage for a more extended investigation into the use of this assay in exploring the pathophysiology of KFD.
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CiteScore
1.30
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审稿时长
11 weeks
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