C. Mattiuzzi, G. Lippi, B. Henry
{"title":"Could body temperature be used as surrogate measure of mRNA-based vaccination efficacy in the general population?","authors":"C. Mattiuzzi, G. Lippi, B. Henry","doi":"10.21037/jlpm-22-59","DOIUrl":null,"url":null,"abstract":"Predicting the humoral, cellular and clinical response to coronavirus disease 2019 (COVID-19) vaccination remains a central aspect for efficiently tackling the ongoing severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic. Several current studies have focused on predicting the clinical response to COVID-19 vaccination by testing both immunological and cellular biomarkers. Nonetheless, this strategy is plagued by a number of drawbacks, so that a \"biological marker\" which may help predicting vaccine efficacy, efficiently surrogating laboratory-based tests, would be a valuable resource for optimizing vaccine delivery. A number of recent studies, summarized in this clinical practice review, have repeatedly emphasized the existence of a significant relationship between increased body temperature and humoral response after mRNA-based COVID-19 vaccination. Therefore, we put forward the idea that fever should be no longer considered only an adverse (almost undesirable) post-vaccination side effect, wherein its onset may actually reflect enhanced immunological response to vaccine, and its measurement could hence be used for screening at least mRNA-based vaccine immunogenicity in terms of humoral response up to 3 months after mRNA-based COVID-19 vaccination by using specifically validated algorithms incorporating the integrate assessment of body temperature and anti-SARS-CoV-2 antibodies.Copyright © Journal of Laboratory and Precision Medicine. All rights reserved.","PeriodicalId":92408,"journal":{"name":"Journal of laboratory and precision medicine","volume":" ","pages":""},"PeriodicalIF":1.4000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of laboratory and precision medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21037/jlpm-22-59","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
在普通人群中,体温是否可以作为mrna疫苗接种效果的替代指标?
预测2019冠状病毒病(新冠肺炎)疫苗接种的体液、细胞和临床反应仍然是有效应对持续的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)大流行的核心方面。目前的几项研究侧重于通过测试免疫学和细胞生物标志物来预测新冠肺炎疫苗接种的临床反应。尽管如此,这一策略仍存在许多缺点,因此,一种可能有助于预测疫苗效力的“生物标志物”,有效地替代实验室测试,将是优化疫苗交付的宝贵资源。本临床实践综述中总结的一些最新研究一再强调,基于mRNA的新冠肺炎疫苗接种后,体温升高与体液反应之间存在显著关系。因此,我们提出了这样的观点,即发烧不应再仅仅被视为疫苗接种后的一种不良(几乎是不可取的)副作用,其中其发作实际上可能反映出对疫苗的免疫反应增强,因此,其测量可用于通过使用结合体温和抗SARS-CoV-2抗体的综合评估的特异性验证算法,在基于mRNA的新冠肺炎疫苗接种后长达3个月的体液反应方面筛选至少基于mRNA的疫苗免疫原性。版权所有©《实验室与精准医学杂志》。保留所有权利。
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