加强剂量的 SARS-COV-2 疫苗可提高炎症性肠病患者的血清转换率。GETECCU前瞻性多中心研究(VACOVEII研究)的结果

Diego Casas Deza , Ana Belén Julián Gomara , Eva Caudevilla Biota , Belén Beltrán , Eugeni Domènech , Ana Gutiérrez Casbas , Miriam Mañosa , Yamile Zabana , Lourdes Roc Alfaro , Emilio Valverde Romero , Elena García González , Beatriz Sicilia , Viviana Laredo , Maria José Alcalá Escriche , Lucia Madero Velázquez , Rocío Ferreiro-Iglesias , Antonia Palmero Pérez , Margalida Calafat , Saioa Rubio Iturria , Irene Moraleja Yudego , Santiago García-López
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引用次数: 0

摘要

背景炎症性肠病(IBD)患者,尤其是接受抗肿瘤坏死因子(anti-TNF)治疗的患者,对接种 SARS-CoV-2 疫苗的反应会降低。然而,有关中期效果的数据却很有限,尤其是使用新推荐的血清转换率(260 BAU/mL)时。我们的目的是评估全程接种和加强免疫后 6 个月的 260 BAU 血清转换率。方法VACOVEII 是由 GETECCU 发起的一项西班牙多中心前瞻性研究。研究对象包括既往未感染过 COVID-19、全程接种过 SARS-CoV-2 疫苗、接受过或未接受过免疫抑制剂治疗的 IBD 患者。加强剂量在全程接种 6 个月后进行。结果在 2021 年 10 月至 2022 年 3 月期间,共纳入了 313 例患者(124 例未接受治疗或使用美沙拉嗪;55 例使用免疫调节剂;87 例使用抗肿瘤坏死因子;19 例使用抗整合素;28 例使用乌司他单抗)。大多数患者接种了 mRNA 疫苗(86%)。全面接种疫苗六个月后,总体血清转换率为 44.1%,服用抗肿瘤坏死因子(19.5%,p < 0.001)和乌斯特库单抗(35.7%,p = 0.031)的患者血清转换率明显较低。强化后的血清转换率为 92%。mRNA疫苗提高了血清转换率(OR 11.720 [95% CI 2.26-60.512])。加强剂量可提高所有患者的血清转换率,但在接受抗肿瘤坏死因子治疗的患者中效果仍然有限。这些结果进一步说明,对于接受免疫抑制剂治疗(尤其是抗肿瘤坏死因子治疗)和使用 mRNA 疫苗的患者,今后需要优先考虑加强剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A booster dose of SARS-COV-2 vaccine improves suboptimal seroconversion rates in patients with inflammatory bowel disease. Results of a prospective multicenter study of GETECCU (VACOVEII study)

Background

The response to SARS-CoV-2 vaccination decreases in inflammatory bowel disease (IBD) patients, specially under anti-TNF treatment. However, data on medium-term effectiveness are limited, specially using new recommended seroconversion rate (>260 BAU/mL). Our aim was to evaluate the 6-month > 260 BAU-seroconversion rate after full vaccination and after booster-dose.

Methods

VACOVEII is a Spanish multicenter, prospective study promoted by GETECCU. IBD patients full vaccinated against SARS-CoV-2 and without previous COVID-19 infection, treated or not with immunosuppressants, were included. The booster dose was administered 6 months after the full vaccination. Seroconversion was set at 260 BAU/mL, according to most recent recommendations and was assessed 6 months after the full vaccination and 6 months after booster-dose.

Results

Between October 2021 and March 2022, 313 patients were included (124 no treatment or mesalazine; 55 immunomodulators; 87 anti-TNF; 19 anti-integrin; and 28 ustekinumab). Most patients received mRNA-vaccines (86%). Six months after full vaccination, overall seroconversion rate was 44.1%, being significantly lower among patients on anti-TNF (19.5%, p < 0.001) and ustekinumab (35.7%, p = 0.031). The seroconversion rate after booster was 92%. Again, anti-TNF patients had a significantly lower seroconversion rate (67%, p < 0.001). mRNA-vaccine improved seroconversion rate (OR 11.720 [95% CI 2.26–60.512]).

Conclusion

The full vaccination regimen achieves suboptimal response in IBD patients, specially among those anti-TNF or ustekinumab. The booster dose improves seroconversion rate in all patients, although it remains limited in those treated with anti-TNF. These results reinforce the need to prioritize future booster doses in patients on immunosuppressants therapy, specially under anti-TNF, and using mRNA-vaccines.
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