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STAR SIGN 研究:评估 COVID-19 疫苗对炎症性肠病患者中 SARS-CoV-2 变异株 BQ.1.1 和 XBB.1.5 的效力。

STAR SIGN study: Evaluation of COVID-19 vaccine efficacy against the SARS-CoV-2 variants BQ.1.1 and XBB.1.5 in patients with inflammatory bowel disease.

机构信息

Max von Pettenkofer Institute of Hygiene and Medical Microbiology, Faculty of Medicine, Ludwig Maximilian University of Munich (LMU Munich), Munich, Germany.

Department of Gastroenterology and Hepatology, Cantonal Hospital St. Gallen, St. Gallen, Switzerland.

出版信息

Aliment Pharmacol Ther. 2023 Oct;58(7):678-691. doi: 10.1111/apt.17661. Epub 2023 Aug 12.

Abstract

BACKGROUND

Vaccine-elicited immune responses are impaired in patients with inflammatory bowel disease (IBD) treated with anti-TNF biologics.

AIMS

To assess vaccination efficacy against the novel omicron sublineages BQ.1.1 and XBB.1.5 in immunosuppressed patients with IBD.

METHODS

This prospective multicentre case-control study included 98 biologic-treated patients with IBD and 48 healthy controls. Anti-spike IgG concentrations and surrogate neutralisation against SARS-CoV-2 wild-type, BA.1, BA.5, BQ.1.1, and XBB.1.5 were measured at two different time points (2-16 weeks and 22-40 weeks) following third dose vaccination. Surrogate neutralisation was based on antibody-mediated blockage of ACE2-spike protein-protein interaction. Primary outcome was surrogate neutralisation against tested SARS-CoV-2 sublineages. Secondary outcomes were proportions of participants with insufficient surrogate neutralisation, impact of breakthrough infection, and correlation of surrogate neutralisation with anti-spike IgG concentration.

RESULTS

Surrogate neutralisation against all tested sublineages was reduced in patients with IBD who were treated with anti-TNF biologics compared to patients treated with non-anti-TNF biologics and healthy controls (each p ≤ 0.001) at visit 1. Anti-TNF therapy (odds ratio 0.29 [95% CI 0.19-0.46]) and time since vaccination (0.85 [0.72-1.00]) were associated with low, and mRNA-1273 vaccination (1.86 [1.12-3.08]) with high wild-type surrogate neutralisation in a β-regression model. Accordingly, higher proportions of patients treated with anti-TNF biologics had insufficient surrogate neutralisation against omicron sublineages at visit 1 compared to patients treated with non-anti-TNF biologics and healthy controls (each p ≤ 0.015). Surrogate neutralisation against all tested sublineages decreased over time but was increased by breakthrough infection. Anti-spike IgG concentrations correlated with surrogate neutralisation.

CONCLUSIONS

Patients with IBD who are treated with anti-TNF biologics show impaired neutralisation against novel omicron sublineages BQ.1.1 and XBB.1.5 and may benefit from prioritisation for future variant-adapted vaccines.

摘要

背景

接受抗 TNF 生物制剂治疗的炎症性肠病 (IBD) 患者的疫苗诱导免疫应答受损。

目的

评估新型 omicron 亚谱系 BQ.1.1 和 XBB.1.5 在免疫抑制的 IBD 患者中的疫苗接种效果。

方法

这项前瞻性多中心病例对照研究纳入了 98 名接受生物治疗的 IBD 患者和 48 名健康对照者。在第三次接种疫苗后 2-16 周和 22-40 周两个不同时间点测量针对 SARS-CoV-2 野生型、BA.1、BA.5、BQ.1.1 和 XBB.1.5 的抗刺突 IgG 浓度和替代中和作用。替代中和作用基于抗体介导的 ACE2-刺突蛋白-蛋白相互作用阻断。主要结局是针对测试的 SARS-CoV-2 亚谱系的替代中和作用。次要结局是评估替代中和作用不足的参与者比例、突破性感染的影响以及替代中和作用与抗刺突 IgG 浓度的相关性。

结果

与接受非抗 TNF 生物制剂治疗的患者和健康对照组相比,接受抗 TNF 生物制剂治疗的 IBD 患者在第 1 次就诊时针对所有测试亚谱系的替代中和作用均降低(均 p≤0.001)。抗 TNF 治疗(比值比 0.29 [95%CI 0.19-0.46])和接种疫苗后的时间(0.85 [0.72-1.00])与低水平的野生型替代中和作用相关,而 mRNA-1273 疫苗接种(1.86 [1.12-3.08])与高水平的野生型替代中和作用相关。因此,与接受非抗 TNF 生物制剂治疗的患者和健康对照组相比,更多接受抗 TNF 生物制剂治疗的患者在第 1 次就诊时针对 omicron 亚谱系的替代中和作用不足(均 p≤0.015)。针对所有测试亚谱系的替代中和作用随时间推移而下降,但突破性感染会增加。抗刺突 IgG 浓度与替代中和作用相关。

结论

接受抗 TNF 生物制剂治疗的 IBD 患者对新型 omicron 亚谱系 BQ.1.1 和 XBB.1.5 的中和作用受损,可能受益于优先接种未来的变异适应疫苗。

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