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
{"title":"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","authors":"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","doi":"10.1080/21645515.2025.2518644","DOIUrl":null,"url":null,"abstract":"<p><p>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, <i>p</i> = .23) against any COVID-19 disease or severe disease (14%, 95%CI: -23 to 39, <i>p</i> = .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, <i>p</i> = .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.</p>","PeriodicalId":49067,"journal":{"name":"Human Vaccines & Immunotherapeutics","volume":"21 1","pages":"2518644"},"PeriodicalIF":3.5000,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12218421/pdf/","citationCount":"0","resultStr":"{\"title\":\"Evaluating the effectiveness of COVID-19 vaccines during a period of Omicron variant predominance among Bangladeshi population: A test-negative design measurement.\",\"authors\":\"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\",\"doi\":\"10.1080/21645515.2025.2518644\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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, <i>p</i> = .23) against any COVID-19 disease or severe disease (14%, 95%CI: -23 to 39, <i>p</i> = .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, <i>p</i> = .023)) for the first 90 days. 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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.
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.