第三剂mRNA COVID-19疫苗的免疫和血液学反应:一项为期六个月的纵向研究

IF 4.8 2区 医学 Q2 IMMUNOLOGY
Frontiers in Cellular and Infection Microbiology Pub Date : 2025-07-10 eCollection Date: 2025-01-01 DOI:10.3389/fcimb.2025.1615227
Waleed M Bawazir, Ahmad Al Ibad, Muneeba Mohsin, Hanouf A Niyazi, Turki A Alamri, Mohammed A Bazuhair, Mohannad Hazzazi, Noura A Chehab, Steve Harakeh, Yasar Mehmood Yousafzai
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引用次数: 0

摘要

针对SARS-CoV-2的mRNA疫苗的部署是控制COVID-19大流行的一个重要里程碑。然而,适应性免疫的激活及其增强剂量后的持续时间值得进一步研究。此外,需要进一步了解转染后炎症和免疫血栓之间的相互作用,以帮助检查疫苗免疫后不良事件(AEFIs)的潜力。本研究调查了68名健康参与者对第三剂COVID-19 mRNA疫苗的生化和血液学反应,这些参与者之前接受过两剂疫苗。在基线(接种疫苗前)采集血样;D0),接种后48小时(D2),然后在第30、60、120和180天(D30、D60、D120、D180)接种。本研究重点分析接种后D2抗sars - cov -2免疫球蛋白(IgG和IgA)、炎症生物标志物(IL-6、IFN-γ、CRP、hs-CRP)、凝血因子(PT、APTT、d -二聚体)和血细胞计数(中性粒细胞、白细胞、血小板)的变化,以及接种后第2、30、60、120和180天IgG和IgA的变化。在这项研究中,没有观察到任何接受者的临床急性脑损伤。在炎症和凝血生物标志物以及血细胞水平上观察到轻微的变化。CRP、hs-CRP水平轻微升高,d-二聚体升高,PT、aPTT明显延长。IFN-γ和平均淋巴细胞计数虽小但显著下降,而D2时IL-6、中性粒细胞和血小板计数水平未见变化。IgG和IgA水平在6个月内持续上升。这些结果共同表明,第三剂mRNA疫苗引起快速和持续的免疫反应,其特征是IgG和IgA水平升高。在接种疫苗后不久观察到的炎症标志物和凝血因子的变化需要进一步调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immune and hematologicak responses to the third dose of an mRNA COVID-19 vaccine: a six-month longitudinal study.

The deployment of mRNA vaccines against SARS-CoV-2 is a major landmark in controlling the COVID-19 pandemic. However, the activation of adaptive immunity and its longevity after a booster dose warrant further investigation. Moreover, the interplay between inflammation and immune thrombosis after transfection needs further insights that could help examine the vaccine's potential for adverse events following immunization (AEFIs). This study investigates the biochemical and hematological responses to the third dose of a COVID-19 mRNA vaccine in 68 healthy participants who had previously received two doses of the vaccine. Blood samples were collected at baseline (before vaccine dose; D0), 48 hours post-vaccination (D2), and then at days 30, 60, 120, and 180 (D30, D60, D120, D180). The study focused on analyzing changes in anti-SARS-COV-2 immunoglobulins (IgG and IgA), inflammatory biomarkers (IL-6, IFN-γ, CRP, hs-CRP), coagulation factors (PT, APTT, D-dimers), and blood cell counts (neutrophils, leukocytes, platelets) at D2 post-vaccination, and IgG and IgA at days 2, 30, 60, 120, and 180 post-vaccination. In this study, no clinical AEFIs were observed in any of the recipients. Slight changes were observed in the levels of inflammatory and coagulation biomarkers, and blood cells. Levels of CRP and hs-CRP increased slightly but significantly, d-dimers were raised, and PT and aPTT were prolonged significantly. A small but significant decrease was observed in IFN-γ and mean lymphocyte counts, whereas no change was observed in the levels of IL-6, neutrophils, and platelet count at D2. Levels of IgG and IgA showed sustained increase over the six-month period. These results collectively demonstrate that the third dose of the mRNA vaccine elicits a rapid and sustained immune response characterized by increased IgG and IgA levels. The changes observed in inflammatory markers and coagulation factors after vaccination observed shortly after vaccination require further investigations.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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