Characteristics of Products of Fibrinogen Origin in the Presence of Anti- SARS-CoV-2 IgG in the Bloodstream.

IF 1.4 Q4 PHARMACOLOGY & PHARMACY Reviews on recent clinical trials Pub Date : 2023-01-01 DOI:10.2174/1574887118666221219115856
Antonina Rachkovska, Daryna Krenytska, Vitalii Karbovskyy, Tetiana Halenova, Nataliia Raksha, Tetiana Vovk, Olexii Savchuk, Dmytro Liubenko, Tetyana Falalyeyeva, Liudmyla Ostapchenko, Ludovico Abenavoli
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引用次数: 2

Abstract

Background: The hemostasis system has been extensively investigated in patients in the acute phase of coronavirus disease 2019 (COVID-19). In contrast, the post-COVID syndrome is a poorly known entity, and there is a lack of information on the mechanisms underlying the hemostasis abnormalities in the post-COVID period.

Aim: To analyze the potential changes in the parameters of the hemostasis system in the post- COVID period in the plasma of donors with different titers of anti-SARS-CoV-2 IgG.

Methods: The plasma from 160 donors who had recovered from COVID infection was used in the study. Based on the results of the Abbott SARS-CoV-2 IgG serological assay, all donors were divided into several groups: 5 ± 3 (n = 20); 55 ± 5 (n = 20); 65 ± 5 (n = 20); 75 ± 5 (n = 20); 85 ± 5 (n = 20); 95 ± 5 (n = 20); 125 ± 5 (n = 20); 175 ± 5 (n = 20) Index (S/C). A total of 20 healthy individuals without anti-SARS-CoV-2 IgG constituted the control group. Key laboratory parameters, such as fibrinogen concentrations, soluble fibrin monomer complex (SFMCs), and Ddimer, were investigated. In addition, the qualitative composition of the fraction of SFMCs was analyzed.

Results: The slight increase in the concentration of fibrinogen, SFMCs, and D-dimers in some donor groups have been found, which could cause the development of hemostasis disorders. In the fraction of SFMCs, the increase in the number of protein fragments with a molecular weight of less than 250 kDa and an increase in the level of proteins with a molecular weight of more than 270 kDa was revealed.

Conclusion: The obtained results indicated the relationship between the changes in the parameters of the hemostasis system and the titers of anti-SARS-CoV-2 IgG in donors in the post-COVID period. It can be assumed that donors with higher titers of anti-SARS-CoV-2 IgG (>55 ± 5 Index (S/C)) are more prone to hemostasis abnormalities in the post-COVID period since a pronounced imbalance in the levels of SFMCs and D-dimer characterizes them. The appearance of protein fragments of different molecular weights in the fraction of SFMC points to uncontrolled activation of biochemical processes involving molecules of fibrinogenic origin. Additional studies are required to elucidate the role of anti-SARS-CoV-2 IgG in the post-COVID period.

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血液中抗SARS-CoV-2 IgG存在时纤维蛋白原产物的特征
背景:对2019冠状病毒病(COVID-19)急性期患者的止血系统进行了广泛的研究。相比之下,covid后综合征是一个鲜为人知的实体,并且缺乏关于covid后时期止血异常的机制的信息。目的:分析不同抗- cov -2 IgG滴度献血者血浆中新冠病毒感染后止血系统参数的潜在变化。方法:采用160例新冠肺炎康复献血者的血浆。根据雅培SARS-CoV-2 IgG血清学检测结果,将所有献血者分为5±3组(n = 20);55±5 (n = 20);65±5 (n = 20);75±5 (n = 20);85±5 (n = 20);95±5 (n = 20);125±5 (n = 20);175±5 (n = 20)指数(S/C)。无抗sars - cov -2 IgG的健康个体20例作为对照组。关键的实验室参数,如纤维蛋白原浓度,可溶性纤维蛋白单体复合物(SFMCs)和二聚体,进行了研究。此外,还对SFMCs组分的定性组成进行了分析。结果:部分供血组纤维蛋白原、SFMCs、d -二聚体浓度轻微升高,可引起止血障碍的发生。在SFMCs片段中,分子量小于250 kDa的蛋白质片段数量增加,分子量大于270 kDa的蛋白质片段水平增加。结论:所得结果提示献血者术后止血系统参数变化与抗sars - cov -2 IgG滴度之间存在相关性。可以认为,抗- cov -2 IgG抗体滴度(>55±5指数(S/C))较高的献血者在covid - 19后更容易出现止血异常,因为他们的SFMCs和d -二聚体水平明显失衡。SFMC部分中不同分子量的蛋白质片段的出现表明涉及纤维蛋白原分子的生化过程的不受控制的激活。需要进一步的研究来阐明抗sars - cov -2 IgG在covid后时期的作用。
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来源期刊
Reviews on recent clinical trials
Reviews on recent clinical trials PHARMACOLOGY & PHARMACY-
CiteScore
3.10
自引率
5.30%
发文量
44
期刊介绍: Reviews on Recent Clinical Trials publishes frontier reviews on recent clinical trials of major importance. The journal"s aim is to publish the highest quality review articles in the field. Topics covered include: important Phase I – IV clinical trial studies, clinical investigations at all stages of development and therapeutics. The journal is essential reading for all researchers and clinicians involved in drug therapy and clinical trials.
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