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评估一种基于微珠的新检测方法,用于测量血浆细胞外囊泡中人类组织因子抗原的水平。

Evaluation of a new bead-based assay to measure levels of human tissue factor antigen in extracellular vesicles in plasma.

作者信息

Archibald Sierra J, Hisada Yohei, Bae-Jump Victoria L, Mackman Nigel

机构信息

Division of Hematology UNC Blood Research Center University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.

Division of Gynecologic Oncology University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.

出版信息

Res Pract Thromb Haemost. 2022 Mar 4;6(2):e12677. doi: 10.1002/rth2.12677. eCollection 2022 Feb.

Abstract

BACKGROUND

Circulating tissue factor (TF)-expressing extracellular vesicles (EVs) are associated with thrombosis in several diseases, such as coronavirus disease 2019 (COVID-19). Activity assays have higher sensitivity and specificity compared to antigen assays for measuring TF+ EVs in plasma. The MACSPlex Exosome Kit is designed to detect 37 exosomal surface epitopes, including TF, on EVs in plasma using various fluorescently labeled beads. The different EV-bead complexes are detected by flow cytometry. A recent study used the MACSPlex Exosome Kit to measure levels of TF+ EVs in serum from patients with COVID-19.

OBJECTIVES

To evaluate the ability of the MACSPlex Exosome Kit to detect TF on EVs in plasma.

METHODS

We measured levels of TF+ EVs isolated from plasma with or without TF detected using our in-house EVTF activity assay and the MACSPlex Exosome Kit.

RESULTS

The MACSPlex Exosome Kit gave a very low TF antigen signal (TF bead signal) compared to platelet-derived CD41b+ EVs, which was used as a control. Lipopolysaccharide (LPS) increased levels of EVTF activity but not TF bead signal in four donors. Inhibition of TF reduced levels of EVTF activity but did not affect the TF bead signal in EVs isolated from plasma from LPS-treated blood. Finally, we found no correlation between levels of EVTF activity and TF bead signal in EVs isolated from plasma from ovarian cancer patients ( = .16,  = .62).

CONCLUSION

Our data suggest that the MACSPlex Exosome Kit gives a nonspecific signal for TF and does not have the sensitivity to detect TF+ EVs in plasma.

摘要

背景

循环中表达组织因子(TF)的细胞外囊泡(EVs)与包括2019冠状病毒病(COVID-19)在内的多种疾病中的血栓形成有关。与抗原检测法相比,活性检测法在测量血浆中TF+ EVs时具有更高的灵敏度和特异性。MACSPlex外泌体试剂盒旨在使用各种荧光标记微珠检测血浆中EVs上的37种外泌体表面表位,包括TF。不同的EV-微珠复合物通过流式细胞术进行检测。最近一项研究使用MACSPlex外泌体试剂盒测量COVID-19患者血清中TF+ EVs的水平。

目的

评估MACSPlex外泌体试剂盒检测血浆中EVs上TF的能力。

方法

我们使用我们的内部EVTF活性检测法和MACSPlex外泌体试剂盒测量从检测到或未检测到TF的血浆中分离出的TF+ EVs的水平。

结果

与用作对照的血小板衍生的CD41b+ EVs相比,MACSPlex外泌体试剂盒给出的TF抗原信号(TF微珠信号)非常低。脂多糖(LPS)增加了四名供体中EVTF活性水平,但未增加TF微珠信号。TF的抑制降低了EVTF活性水平,但不影响从LPS处理血液的血浆中分离出的EVs中的TF微珠信号。最后,我们发现从卵巢癌患者血浆中分离出的EVs中,EVTF活性水平与TF微珠信号之间没有相关性(r = 0.16,P = 0.62)。

结论

我们的数据表明,MACSPlex外泌体试剂盒给出的是TF的非特异性信号,并且没有检测血浆中TF+ EVs的灵敏度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c24a/8897283/86d39396d920/RTH2-6-e12677-g001.jpg

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