The Impact of Vaccination and SARS-CoV-2 Variants on the Virological Response to SARS-CoV-2 Infections during the Alpha, Delta, and Omicron waves in England.

Rachel Lunt, Catherine Quinot, Freja Kirsebom, N. Andrews, Catriona Skarnes, Louise Letley, D. Haskins, Catriona Angel, Skye Firminger, Kay Ratcliffe, Shelina Rajan, Angela Sherridan, Samreen Ijaz, M. Zambon, Kevin Brown, M. Ramsay, J. L. Bernal
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Abstract

Vaccination status and the SARS-CoV-2 variant individuals are infected with are known to independently impact viral dynamics; however, little is known about the interaction of these two factors and how this impacts viral dynamics. Here we investigated how monovalent vaccination modified the time course and viral load of infections from different variants. Regression analyses were used to investigate the impact of vaccination on cycle threshold values and disease severity, and interval-censored survival analyses were used to investigate the impact of vaccination on duration of positivity. A range of covariates were adjusted for as potential confounders and investigated for their own effects in exploratory analyses. All analyses were done combining all variants and stratified by variant. For those infected with Alpha or Delta, vaccinated individuals were more likely to report mild disease than moderate/severe disease and had significantly shorter duration of positivity and lower viral loads compared to unvaccinated individuals. Vaccination had no impact on self-reported disease severity, viral load, or duration if positivity for those infected with Omicron. Overall, individuals who were immunosuppressed and clinically extremely vulnerable had longer duration of positivity and higher viral loads. This study adds to the evidence base on disease dynamics following COVID-19, demonstrating that vaccination mitigates severity of disease, the amount of detectable virus within infected individuals and reduces the time individuals are positive for. However, these effects have been significantly attenuated since the emergence of Omicron. Therefore, our findings strengthen the argument for using modified or multivalent vaccines that target emerging variants.
疫苗接种和 SARS-CoV-2 变异株对英国阿尔法、德尔塔和奥米克隆波期间 SARS-CoV-2 感染的病毒学反应的影响》(The Impact of Vaccination and SARS-CoV-2 Variants on the Virological Response to SARS-CoV-2 Infections during the Alpha, Delta, and Omicron waves in England.
众所周知,疫苗接种情况和个体感染的 SARS-CoV-2 变异株会单独影响病毒的动态变化;然而,人们对这两个因素之间的相互作用以及这种相互作用如何影响病毒动态变化却知之甚少。在此,我们研究了单价疫苗接种如何改变不同变异株感染的时间进程和病毒载量。回归分析用于研究接种疫苗对周期阈值和疾病严重程度的影响,间隔删失生存分析用于研究接种疫苗对阳性持续时间的影响。在探索性分析中,将一系列协变量作为潜在的混杂因素进行了调整,并研究了它们本身的影响。所有分析均结合所有变异体进行,并按变异体进行分层。对于阿尔法或德尔塔病毒感染者,与未接种疫苗者相比,接种疫苗者更有可能报告轻度疾病,而非中度/重度疾病,并且阳性持续时间明显更短,病毒载量更低。接种疫苗对感染了奥米克龙病毒的人自我报告的疾病严重程度、病毒载量或阳性持续时间没有影响。总体而言,免疫抑制者和临床极度脆弱者的阳性持续时间更长,病毒载量更高。这项研究补充了 COVID-19 后疾病动态的证据基础,表明接种疫苗可减轻疾病的严重程度、减少感染者体内可检测到的病毒数量并缩短病毒呈阳性的时间。然而,自 Omicron 出现以来,这些效果已明显减弱。因此,我们的研究结果加强了使用针对新变种的改良疫苗或多价疫苗的论据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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