在孟加拉国人群中欧米克隆变异优势期评估COVID-19疫苗的有效性:检测阴性设计测量

IF 3.5 4区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Human Vaccines & Immunotherapeutics Pub Date : 2025-12-01 Epub Date: 2025-06-28 DOI:10.1080/21645515.2025.2518644
Md Taufiqul Islam, Farhana Khanam, Faisal Ahmmed, Md Nazmul Hasan Rajib, Md Ismail Hossen, Shahinur Haque, Prasanta Kumar Biswas, Shah Ali Akbar Ashrafi, Ahmed Nawsher Alam, Mallick Masum Billah, Monalisa, Mohammed Ziaur Rahman, Omar Hamza Bin Manjur, Mohammad Tanbir Habib, Mokibul Hassan Afrad, S M Shamsuzzaman, Ahmed Abu Saleh, Mostafa Aziz Sumon, Asif Rashed, Tahmina Shirin, John D Clemens, Firdausi Qadri
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引用次数: 0

摘要

进行这项研究是为了估计在孟加拉国部署的COVID-19疫苗的完整初级或加强剂量方案的保护有效性(PE)。该研究于2021年12月30日至2022年8月31日期间在达卡的四家医院进行,设计为阴性。纳入年龄≥18岁且出现covid -样症状的患者,并进行RT-PCR检测。考虑地点、日期和年龄组,检测阴性对照与确诊病例按1:1的比例匹配。使用条件logistic回归来估计PE,考虑到接受完整的初级治疗并或不接受强化治疗与COVID-19疾病症状的发展之间的关联。采用全基因组测序(WGS)对变异进行确证。RT-PCR阳性847例,对照847例。WGS结果显示,6%的菌株为δ变异,94%的菌株为欧米克隆变异。接受完整的初级方案(含或不含任何疫苗加强剂)所赋予的PE显示,对任何COVID-19疾病或严重疾病没有显著的保护作用(15%,95%CI: -11至36,p = 0.23) (14%, 95%CI: -23至39,p = 0.42)。然而,在前90天接受完整的初级方案与不接受一种mRNA疫苗(辉瑞- biontech)加强剂量之间存在保护性关联(88% (95% CI: 26至98,p = 0.023)),以预防任何COVID-19疾病。分析表明,在Omicron激增期间,疫苗几乎没有效力,可能在给药90天后有一种mrna疫苗例外。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating the effectiveness of COVID-19 vaccines during a period of Omicron variant predominance among Bangladeshi population: A test-negative design measurement.

The study was conducted to estimate the protective effectiveness (PE) of complete primary or booster dose regimens of COVID-19 vaccines deployed in Bangladesh. The study was conducted in four hospitals in Dhaka between December 30, 2021, and August 31, 2022 following a test-negative design. Patients aged ≥18 years attended with COVID-like symptoms were enrolled and tested for RT-PCR. Test-negative controls were matched to confirmed cases at a 1:1 ratio considering site, date, and age groups. Conditional logistic regression was used to estimate the PE considering the association between receipt of complete primary with or without a booster regimen and development of COVID-19 disease symptoms. Whole genome sequencing (WGS) was carried out to confirm the variants. RT-PCR positive 847 cases were matched to 847 controls. WGS of strains revealed 6% to be the Delta variant and 94% was Omicron variant. The PE conferred by receipt of complete primary regimen with or without booster dose of any vaccine revealed no significant protection (15%, 95% CI: -11 to 36, p = .23) against any COVID-19 disease or severe disease (14%, 95%CI: -23 to 39, p = .42). However, there was a protective association between receipt of complete primary regimen with or without booster dose of one mRNA vaccine (Pfizer-BioNTech) against any COVID-19 disease (88% (95% CI: 26 to 98, p = .023)) for the first 90 days. The analysis suggested little vaccine effectiveness during Omicron surge, with the possible exception of one mRNA-vaccine 90 days after dosing.

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来源期刊
Human Vaccines & Immunotherapeutics
Human Vaccines & Immunotherapeutics BIOTECHNOLOGY & APPLIED MICROBIOLOGY-IMMUNOLOGY
CiteScore
7.90
自引率
8.30%
发文量
489
审稿时长
3-6 weeks
期刊介绍: (formerly Human Vaccines; issn 1554-8619) Vaccine research and development is extending its reach beyond the prevention of bacterial or viral diseases. There are experimental vaccines for immunotherapeutic purposes and for applications outside of infectious diseases, in diverse fields such as cancer, autoimmunity, allergy, Alzheimer’s and addiction. Many of these vaccines and immunotherapeutics should become available in the next two decades, with consequent benefit for human health. Continued advancement in this field will benefit from a forum that can (A) help to promote interest by keeping investigators updated, and (B) enable an exchange of ideas regarding the latest progress in the many topics pertaining to vaccines and immunotherapeutics. Human Vaccines & Immunotherapeutics provides such a forum. It is published monthly in a format that is accessible to a wide international audience in the academic, industrial and public sectors.
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