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贝伐单抗和阿柏西普通过FcγRIIa激活血小板。

Bevacizumab and Aflibercept Activate Platelets via FcγRIIa.

作者信息

Nomura Yoko, Kaneko Makoto, Miyata Kanjiro, Yatomi Yutaka, Yanagi Yasuo

机构信息

Department of Ophthalmology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo, Tokyo, Japan.

Department of Clinical Laboratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

出版信息

Invest Ophthalmol Vis Sci. 2015 Dec;56(13):8075-82. doi: 10.1167/iovs.15-17814.

Abstract

PURPOSE

To confirm the formation of a drug-growth factor complex and investigate the effects of three VEGF inhibitors in the activation of platelets.

METHODS

Growth factors and individual drugs were mixed and incubated. Scattered light intensity was measured by dynamic light scattering (DLS) to monitor the formation of drug-growth factor complex. Blood samples were obtained from 16 subjects (5 AMD patients and 11 healthy volunteers). Platelets obtained from the platelet-rich fraction by centrifugation were washed and resuspended in HEPES/Tyrode buffer. Platelet aggregability was assessed using a light transmission aggregometer in the presence of VEGF inhibitors and growth factors.

RESULTS

In DLS study, a mixture of bevacizumab and VEGF-A showed one peak with a relatively gentle slope, indicating a heterogeneous mixture of multimeric bevacizumab-VEGF-A complexes. In aggregation study, no detectable aggregation was observed in the presence of ranibizumab, while significant aggregation was observed in the presence of VEGF-A and bevacizumab in five cases (one AMD patient and four healthy volunteers), VEGF-B and aflibercept in two cases (two volunteers), and placental growth factor (PlGF) and aflibercept in one case (one volunteer). No aggregation was observed when FcγRIIa antibody was added beforehand.

CONCLUSIONS

A complex composed of bevacizumab or aflibercept, but not ranibizumab, and growth factors activates platelets via FcγRIIa.

摘要

目的

确认药物-生长因子复合物的形成,并研究三种血管内皮生长因子(VEGF)抑制剂对血小板活化的影响。

方法

将生长因子与各药物混合并孵育。通过动态光散射(DLS)测量散射光强度,以监测药物-生长因子复合物的形成。从16名受试者(5例年龄相关性黄斑变性(AMD)患者和11名健康志愿者)采集血样。通过离心从富含血小板的部分获得的血小板经洗涤后重悬于HEPES/泰罗德缓冲液中。在VEGF抑制剂和生长因子存在的情况下,使用透光率聚集仪评估血小板聚集性。

结果

在DLS研究中,贝伐单抗与VEGF-A的混合物显示出一个斜率相对平缓的峰,表明多聚体贝伐单抗-VEGF-A复合物的混合物具有异质性。在聚集研究中,在雷珠单抗存在的情况下未观察到可检测到的聚集,而在5例(1例AMD患者和4名健康志愿者)中,在VEGF-A和贝伐单抗存在时观察到显著聚集;在2例(2名志愿者)中,在VEGF-B和阿柏西普存在时观察到显著聚集;在1例(1名志愿者)中,在胎盘生长因子(PlGF)和阿柏西普存在时观察到显著聚集。预先添加FcγRIIa抗体时未观察到聚集。

结论

由贝伐单抗或阿柏西普而非雷珠单抗与生长因子组成的复合物通过FcγRIIa激活血小板。

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