Sarjomaa Marjut, Berg Kristine Karlsrud, Jaioun Keson, Tveten Yngvar, Kersten Hege, Reiso Harald, Eikeland Randi, Thilesen Carina, Nordbø Svein Arne, Aaberge Ingeborg S, Pearce Neil, Fell Anne Kristin Moeller
Department of Infection Control, Telemark Hospital Trust, Ulefossvegen 55, 3710, Skien, Norway.
Department of Community Medicine and Global Health, University of Oslo, Oslo, Norway.
BMC Med. 2025 Jun 3;23(1):332. doi: 10.1186/s12916-025-04171-2.
We have previously reported on natural humoral immunity against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in a Norwegian cohort between 2020 and 2021. In this study, we evaluated long-term humoral (including vaccination-induced) immunity in the same cohort and assessed predictors of high antibody levels against spike protein, as well as the persistence of antibodies against the virus spike and nucleocapsid proteins.
Vaccination data and antibody levels against the spike and nucleocapsid proteins were collected at 12 (only in infected participants) and 24 months (in both infected and uninfected participants) after the participants' first polymerase chain reaction (PCR) tests for the virus. Antibody levels against spike protein at 24 months were categorized as high or low based on the 50th percentile. Possible predictors of high antibody levels against spike protein were examined using univariate and multivariate logistic regression models.
Of 1119 original participants (400 PCR + and 719 PCR -), 574 responded to our questionnaires and were invited to antibody measurements (median age: 51 years; women: 59%). Vaccination data showed that 11% were fully immunized, and 85% were booster-immunized at 24 months. Antibody levels were evaluated in 72% (287/400) of the PCR + participants at 12 months and 58% (233/400) at 24 months. At 12 and 24 months, we observed that 97% (278/287) and 100% (233/233), respectively, still had antibodies against the spike protein, and 86% (248/287) and 95% (221/233), respectively, against the nucleocapsid protein. Antibody levels were also evaluated in 34% (247/719) of those in the PCR - group, which revealed that 99.5% and 69% had detectable antibodies against spike and nucleocapsid proteins, respectively, at 24 months. Irrespective of pre-vaccination SARS-CoV-2 infection status, the booster-immunized participants were 3.7 × more likely to have high antibody levels against spike protein vs the non-booster-immunized ones. Those aged > 60 years had the highest median antibody levels against the spike protein and were more likely to be booster-immunized.
Our findings highlight the benefits of booster vaccinations for humoral immune responses. Long-term antibody levels against the SARS-CoV-2 spike protein were higher in booster-immunized participants vs the non-booster-immunized, irrespective of pre-vaccination infection status.
146,469: The COVID-19 study in Telemark and Agder-COVITA.
gov ID: NCT04514003.
我们之前报道过2020年至2021年挪威一个队列中针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的天然体液免疫情况。在本研究中,我们评估了同一队列中的长期体液免疫(包括疫苗诱导的免疫),并评估了针对刺突蛋白的高抗体水平的预测因素,以及针对病毒刺突蛋白和核衣壳蛋白的抗体持久性。
在参与者首次进行病毒聚合酶链反应(PCR)检测后的12个月(仅针对感染参与者)和24个月(针对感染和未感染参与者)收集疫苗接种数据以及针对刺突蛋白和核衣壳蛋白的抗体水平。根据第50百分位数将24个月时针对刺突蛋白的抗体水平分为高或低。使用单变量和多变量逻辑回归模型检查针对刺突蛋白的高抗体水平的可能预测因素。
在1119名原始参与者(400名PCR检测呈阳性和719名PCR检测呈阴性)中,574人回复了我们的问卷并被邀请进行抗体检测(中位年龄:51岁;女性:59%)。疫苗接种数据显示,11%的人在24个月时已完全接种疫苗,85%的人接受了加强免疫。在PCR检测呈阳性的参与者中,72%(287/400)在12个月时接受了抗体水平评估,58%(233/400)在24个月时接受了评估。在12个月和24个月时,我们观察到分别有97%(278/287)和100%(233/233)的人仍有针对刺突蛋白的抗体,分别有86%(248/287)和95%(221/233)的人有针对核衣壳蛋白的抗体。在PCR检测呈阴性的组中,34%(247/719)的人也接受了抗体水平评估,结果显示在24个月时,分别有99.5%和69%的人有可检测到的针对刺突蛋白和核衣壳蛋白的抗体。无论接种疫苗前的SARS-CoV-2感染状态如何,接受加强免疫的参与者针对刺突蛋白的高抗体水平的可能性是未接受加强免疫者的3.7倍。年龄大于60岁的人针对刺突蛋白的中位抗体水平最高,且更有可能接受加强免疫。
我们的研究结果突出了加强疫苗接种对体液免疫反应的益处。无论接种疫苗前的感染状态如何,接受加强免疫的参与者针对SARS-CoV-2刺突蛋白的长期抗体水平高于未接受加强免疫者。
146,469:泰勒马克和阿格德尔的COVID-19研究——COVITA。临床试验:gov标识符:NCT04514003。