Persistent SARS-COV-2 infection in vaccinated individual with three doses of COVID-19 vaccine

IF 4.5 3区 医学 Q2 IMMUNOLOGY
Germana Silva Vasconcelos, Maria da Conceição Rodrigues Fernandes, Tamires Cardoso Matsui, Maria Claudia dos Santos Luciano, Cecilia Leite Costa, Clarissa Perdigão Mello Ferraz, Fernando Braga Stehling Dias, Fabio Miyajima, Fernanda Montenegro de Carvalho Araújo, Marcela Helena Gambim Fonseca
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Abstract

We describe a case of a 24-year-old Brazilian woman previously vaccinated with CoronaVac and a booster dose of Pfizer-BioNTech, with mild-to-moderate COVID-19, with persistent viral shedding. We evaluated viral load, antibody dynamics for SARS-CoV-2 and performed genomic analysis to identify the viral variant. The female remained positive for 40 days following symptom onset (cycle quantification mean: 32.54 ± 2.29). The humoral response was characterized by absence of IgM for the viral spike protein, increased IgG for the viral spike (1800.60 to 19558.60 AU/mL) and for the nucleocapsid (from 0.03 to 8.9 index value) proteins, and high titers of neutralizing antibodies (>488.00 IU/mL). The variant identified was the sublineage BA. 5.1. of Omicron (B.1.1.529). Our results suggest that even though the female produced an antibody response against SARS-CoV-2, the persistent infection can be explained by antibody decline and/or the immune evasion by the Omicron variant, illustrating the need to revaccinate or update vaccines.

Abstract Image

Abstract Image

Abstract Image

接种三剂COVID-19疫苗的个体持续感染SARS-COV-2
我们描述了一例24岁的巴西妇女,她之前接种了CoronaVac和加强剂量的Pfizer-BioNTech,患有轻度至中度新冠肺炎,并持续脱落病毒。我们评估了严重急性呼吸系统综合征冠状病毒2型的病毒载量和抗体动力学,并进行了基因组分析以确定病毒变体。女性在症状出现后40天内保持阳性(周期定量平均值:32.54±2.29)。体液反应的特征是缺乏病毒刺突蛋白的IgM,增加病毒刺突的IgG(1800.60至19558.60 AU/mL)和核衣壳蛋白(0.03至8.9指数值),和高滴度的中和抗体(>488.00IU/mL)。奥密克戎(B.1.1.529)。我们的研究结果表明,尽管女性产生了针对严重急性呼吸系统综合征冠状病毒2型的抗体反应,但持续感染可以通过抗体下降和/或奥密克戎变异株的免疫逃避来解释,这说明需要重新接种或更新疫苗。
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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
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