Timing and sequence of vaccination against COVID-19 and influenza (TACTIC): a single-blind, placebo-controlled randomized clinical trial

被引:25
作者
Dulfer, Elisabeth A. [1 ,2 ]
Geckin, Buesra [1 ,2 ]
Taks, Esther J. M. [1 ,2 ]
GeurtsvanKessel, Corine H. [3 ]
Dijkstra, Helga [1 ,2 ]
van Emst, Liesbeth [1 ,2 ]
van der Gaast-de Jongh, Christa E. [4 ]
van Mourik, Djenolan [3 ]
Koopmans, Petra C. [5 ]
Dominguez-Andres, Jorge [1 ,2 ]
van Crevel, Reinout [1 ,2 ]
van de Maat, Josephine S. [1 ,2 ]
de Jonge, Marien I. [2 ,4 ]
Netea, Mihai G. [1 ,2 ,6 ]
机构
[1] Radboud Univ Nijmegen, Dept Internal Med, Med Ctr, Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Radboud Ctr Infect Dis, Med Ctr, Nijmegen, Netherlands
[3] Erasmus MC, Lab Virosci, Rotterdam, Netherlands
[4] Radboud Univ Nijmegen, Lab Med Immunol, Med Ctr, Nijmegen, Netherlands
[5] Radboud Univ Nijmegen, Dept Biostat, Med Ctr, Nijmegen, Netherlands
[6] Univ Bonn, Life & Med Sci Inst LIMES, Dept Immunol & Metab, Bonn, Germany
来源
LANCET REGIONAL HEALTH-EUROPE | 2023年 / 29卷
关键词
COVID-19; SARS-CoV2; Infection; Infectious diseases; Vaccines; mRNA; Influenza; VACCINES; MEASLES; IMMUNOGENICITY; RUBELLA; SAFETY; MUMPS;
D O I
10.1016/j.lanepe.2023.100628
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background Novel mRNA-based vaccines have been used to protect against SARS-CoV-2, especially in vulnerable populations who also receive an annual influenza vaccination. The TACTIC study investigated potential immune interference between the mRNA COVID-19 booster vaccine and the quadrivalent influenza vaccine, and determined if concurrent administration would have effects on safety or immunogenicity.Methods TACTIC was a single-blind, placebo-controlled randomized clinical trial conducted at the Radboud University Medical Centre, the Netherlands. Individuals & GE;60 years, fully vaccinated against COVID-19 were eligible for participation and randomized into one of four study groups: 1) 0.5 ml influenza vaccination Vaxigrip Tetra followed by 0.3 ml BNT162b2 COVID-19 booster vaccination 21 days later, (2) COVID-19 booster vaccination followed by influenza vaccination, (3) influenza vaccination concurrent with the COVID-19 booster vaccination, and (4) COVID-19 booster vaccination only (reference group). Primary outcome was the geometric mean concentration (GMC) of IgG against the spike (S)-protein of the SARS-CoV-2 virus, 21 days after booster vaccination. We performed a non-inferiority analysis of concurrent administration compared to booster vaccines alone with a predefined non-inferiority margin of -0.3 on the log10-scale.Findings 154 individuals participated from October, 4, 2021, until November, 5, 2021. Anti-S IgG GMCs for the co -administration and reference group were 1684 BAU/ml and 2435 BAU/ml, respectively. Concurrent vaccination did not meet the criteria for non-inferiority (estimate -0.1791, 95% CI -0.3680 to -0.009831) and antibodies showed significantly lower neutralization capacity compared to the reference group. Reported side-effects were mild and did not differ between study groups.Interpretation Concurrent administration of both vaccines is safe, but the quantitative and functional antibody re-sponses were marginally lower compared to booster vaccination alone. Lower protection against COVID-19 with concurrent administration of COVID-19 and influenza vaccination cannot be excluded, although additional larger studies would be required to confirm this.Trial registration number EudraCT: 2021-002186-17Funding The study was supported by the ZonMw COVID-19 Programme.Copyright & COPY; 2023 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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