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SARS-CoV-2 抗体疫苗在抗核衣壳血清学阳性或有 COVID-19 感染史的炎症性肠病患者中的反应。

SARS-CoV-2 antibody vaccine response in Inflammatory Bowel Disease patients with positive anti-nucleocapsid serology or history of COVID-19 infection.

机构信息

Department of Gastroenterology, Hepatopancreatology, and Digestive Oncology, HUB Hôpital Erasme, Université Libre de Bruxelles, Brussels Belgium.

Department of Hepato-Gastroenterology, CHU Saint-Pierre, Université Libre de Bruxelles, Brussels, Belgium.

出版信息

Acta Gastroenterol Belg. 2024 Apr-Jun;87(2):263-273. doi: 10.51821/87.2.12805.

Abstract

BACKGROUND

Previous history of COVID-19 infection is a natural booster of the vaccine response in the general population. The response to COVID-19 vaccines is lessened in Inflammatory Bowel Disease patients on selected class of immunosuppressive treatments.

AIMS

The study was to assess anti-SARS-CoV-2 spike-specific IgG antibody response in Inflammatory Bowel Disease patients with a history of COVID-19 infection.

PATIENTS AND METHODS

This single-center prospective study involved 504 Inflammatory Bowel Disease patients. Demographic data and clinical data were gathered through questionnaires and patient charts. Anti-SARS-CoV-2 spike-specific and antinucleocapsid antibody levels were measured at T1, T2 (after the 2-dose series), and T3 or T4 (booster vaccine).

RESULTS

This study included 504 Inflammatory Bowel Disease patients, and 234 completed one year follow-up with blood tests. Positive anti-nucleocapsid serology or history of COVID-19 infection was significantly associated with increased median anti- SARS-CoV-2 spike-specific IgG titers after the 2-dose series (1930 BAU/mL vs. 521 BAU/mL p < 0.0001) and the booster vaccine (4390 BAU/mL vs. 2160 BAU/mL, p = 0.0156). Multivariate analysis showed that higher anti-SARS-CoV-2 spike-specific IgG levels were independently associated with anti-nucleocapsid antibodies at T2 (OR=2.23, p < 0.0001) and T3 (OR=1.72, p = 0.00011). Immunosuppressive treatments did not impact the antibody response or levels in patients with a history of COVID-19 infection or positive anti-nucleocapsid serology.

CONCLUSIONS

In Inflammatory Bowel Disease, prior COVID-19 infection or positive anti-nucleocapsid serology leads to increased anti-SARS-CoV-2 spike-specific IgG levels after vaccination, regardless of immunosuppressive treatments. This emphasizes the significance of accounting for previous infection in vaccination approaches.

摘要

背景

先前的 COVID-19 感染史是普通人群中疫苗反应的自然增强剂。在接受特定类别的免疫抑制治疗的炎症性肠病患者中,COVID-19 疫苗的反应会减弱。

目的

本研究旨在评估有 COVID-19 感染史的炎症性肠病患者对 SARS-CoV-2 刺突特异性 IgG 抗体的反应。

患者和方法

这是一项单中心前瞻性研究,共纳入 504 例炎症性肠病患者。通过问卷和患者病历收集人口统计学数据和临床数据。在 T1、T2(两剂系列后)和 T3 或 T4(加强疫苗)时测量抗 SARS-CoV-2 刺突特异性和抗核衣壳抗体水平。

结果

本研究纳入了 504 例炎症性肠病患者,其中 234 例完成了一年的随访和血液检查。抗核衣壳血清学阳性或 COVID-19 感染史与两剂系列后 SARS-CoV-2 刺突特异性 IgG 滴度升高显著相关(1930 BAU/mL 与 521 BAU/mL,p < 0.0001)和加强疫苗(4390 BAU/mL 与 2160 BAU/mL,p = 0.0156)。多变量分析显示,T2(OR=2.23,p < 0.0001)和 T3(OR=1.72,p = 0.00011)时更高的抗 SARS-CoV-2 刺突特异性 IgG 水平与抗核衣壳抗体独立相关。免疫抑制治疗并未影响有 COVID-19 感染史或抗核衣壳血清学阳性患者的抗体反应或水平。

结论

在炎症性肠病中,先前的 COVID-19 感染或抗核衣壳血清学阳性导致接种疫苗后 SARS-CoV-2 刺突特异性 IgG 水平升高,无论免疫抑制治疗如何。这强调了在疫苗接种方法中考虑既往感染的重要性。

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