Infectious Diseases Unit, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
School of Medicine and Surgery, University of Milano-Bicocca, Milan, Italy.
Infection. 2024 Aug;52(4):1499-1509. doi: 10.1007/s15010-024-02250-9. Epub 2024 Apr 23.
Antibodies against SARS-CoV-2 spike (anti-S) may confer protection against symptomatic COVID-19. Whether their level predicts progression among those with COVID-19 pneumonia remains unclear.
We conducted a retrospective cohort study to assess predictors of anti-S levels and whether anti-S titer is associated with death or mechanical ventilation (MV). Adults hospitalized for COVID-19 pneumonia between July 2021 and July 2022 were enrolled if anti-S had been measured within 72 h of admission. Predictors of anti-S level were explored using multivariable quantile regression. The association between anti-S levels and 30-day death/MV was investigated via multivariable logistic regression. Analyses were stratified by vaccine status.
The median anti-S level was 1370 BAU/ml in 328 vaccinated and 15.5 BAU/ml in 206 unvaccinated individuals. Among the vaccinated, shorter symptom duration (p = 0.001), hematological malignancies (p = 0.002), and immunosuppressive therapy (p = 0.004) were associated with lower anti-S levels. In the unvaccinated group, symptom duration was the only predictor of anti-S levels (p < 0.001). After 30 days, 134 patients experienced death or MV. Among vaccinated individuals, higher anti-S levels correlated significantly with lower death/MV risk (per log increase, OR 0.88, 95%CI 0.81-0.97), irrespective of age and solid malignancies. Among unvaccinated, a marginally protective effect was observed (OR 0.86, 95%CI 0.73-1.01), independent of age, immunosuppressive therapy, and diabetes. Adjustment for monoclonal antibody treatment strengthened the association (OR 0.81, 95%CI 0.68-0.96).
This study suggests that levels of anti-S antibodies can predict critical or fatal outcomes in COVID-19 pneumonia patients, regardless of vaccination. Whether anti-S Ab could guide risk assessment and vaccination boosting merits further evaluation.
针对严重急性呼吸综合征冠状病毒 2 刺突蛋白(anti-S)的抗体可能对有症状的 COVID-19 提供保护。然而,其水平是否能预测 COVID-19 肺炎患者的病情进展尚不清楚。
我们进行了一项回顾性队列研究,以评估抗 S 水平的预测因素,以及抗 S 滴度是否与死亡或机械通气(MV)相关。如果在入院后 72 小时内测量了抗 S,则将 2021 年 7 月至 2022 年 7 月期间因 COVID-19 肺炎住院的成年人纳入研究。使用多变量分位数回归来探讨抗 S 水平的预测因素。通过多变量逻辑回归研究抗 S 水平与 30 天死亡/MV 的关系。根据疫苗接种情况对分析进行分层。
在 328 名接种疫苗和 206 名未接种疫苗的个体中,抗 S 水平的中位数分别为 1370 BAU/ml 和 15.5 BAU/ml。在接种疫苗的个体中,症状持续时间较短(p=0.001)、血液系统恶性肿瘤(p=0.002)和免疫抑制治疗(p=0.004)与较低的抗 S 水平相关。在未接种疫苗的人群中,症状持续时间是唯一预测抗 S 水平的因素(p<0.001)。30 天后,134 名患者出现死亡或 MV。在接种疫苗的个体中,较高的抗 S 水平与较低的死亡/MV 风险显著相关(每增加一个对数,OR 0.88,95%CI 0.81-0.97),与年龄和实体恶性肿瘤无关。在未接种疫苗的人群中,观察到边缘保护作用(OR 0.86,95%CI 0.73-1.01),与年龄、免疫抑制治疗和糖尿病无关。调整单克隆抗体治疗后,该关联得到了加强(OR 0.81,95%CI 0.68-0.96)。
这项研究表明,针对严重急性呼吸综合征冠状病毒 2 刺突蛋白的抗体水平可以预测 COVID-19 肺炎患者的重症或致死结局,无论是否接种疫苗。抗 S Ab 是否可以指导风险评估和疫苗加强接种值得进一步评估。