Blood:PF4-VWF-HIT抗体复合物在肝素诱导的血小板减少症发病过程中的作用

2020-02-21 不详 MedSci原创

中心点:PF4与VWF结合形成抗原复合物,被HIT抗体识别。PF4-VWF-HIT抗体复合物通过血小板FcγRIIA和GPIb-IX受体 增强血小板粘附。摘要:肝素诱导的血小板减少症(HIT)是一种由血小板因子4 (PF4)和肝素或其他多阴离子之间的复合物介导的血栓前期疾病,但血栓形成的风险高于与其他PF4伴侣相关的肝素暴露的。近期,Johnston等发现血栓周围内皮细胞被HIT抗体攻击,但结合位

中心点:

PF4与VWF结合形成抗原复合物,被HIT抗体识别。

PF4-VWF-HIT抗体复合物通过血小板FcγRIIA和GPIb-IX受体 增强血小板粘附。

摘要:

肝素诱导的血小板减少症(HIT)是一种由血小板因子4 (PF4)和肝素或其他多阴离子之间的复合物介导的血栓前期疾病,但血栓形成的风险高于与其他PF4伴侣相关的肝素暴露的。近期,Johnston等发现血栓周围内皮细胞被HIT抗体攻击,但结合位点尚未明确。

在本研究中,Johnston等人发现,在流动的内皮化微流体系统中,光化学损伤后,PF4与内皮细胞释放的VWF的延伸链表面上的多个离散位点结合。HIT样单克隆抗体KKO和HIT患者抗体可识别PF4-VWF复合物,促进血小板粘附和微流体通道内血栓的增大。

血小板对PF4-VWF-HIT抗体复合物的粘附被可封闭FcgRIIA或血小板上的糖蛋白Ib-IX复合物的抗体所抑制。用可阻断或封闭VWF寡聚作用的药物破坏PF4-VWF-HIT抗体复合物可减少HIT小鼠模型的血栓形成。

总而言之,本研究表明,HIT免疫复合物沿受损内皮细胞释放的VWF延伸链组装,可能会增加HIT血栓形成的风险。破坏PF4-VWF复合物的形成或可为HIT的治疗提供新的思路。

原始出处:


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    2021-06-16 shengdai3

    学习了

    0

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    2020-08-20 sunmin0229
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    2020-04-29 yuandd
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    2020-02-23 sunmin0219
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    2020-02-21 qingfengqishi5

    学习了,学习了

    0