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Review
. 2023 Jan 19;11(2):224.
doi: 10.3390/vaccines11020224.

A Systematic Review and Meta-Analysis on the Real-World Effectiveness of COVID-19 Vaccines against Infection, Symptomatic and Severe COVID-19 Disease Caused by the Omicron Variant (B.1.1.529)

Affiliations
Review

A Systematic Review and Meta-Analysis on the Real-World Effectiveness of COVID-19 Vaccines against Infection, Symptomatic and Severe COVID-19 Disease Caused by the Omicron Variant (B.1.1.529)

Hassen Mohammed et al. Vaccines (Basel). .

Abstract

Real-world data on the effectiveness of COVID-19 vaccines against the Omicron variant (B.1.1.529) is limited. This systematic review aimed to investigate the real-world effectiveness and durability of protection conferred by primary course and booster vaccines against confirmed Omicron infection, and severe outcomes. We systematically searched literature up to 1 August 2022. Meta-analysis was performed with the DerSimonian-Laird random-effects model to estimate the pooled vaccine effectiveness (VE). Overall, 28 studies were included representing 11 million individuals. The pooled VE against Omicron infection was 20.4% (95%CI: 12.1-28.7%) and 23.4% (95%CI: 13.5-33.3%) against symptomatic infection with variation based on vaccine type and age groups. VE sharply declined from 28.1% (95%CI: 19.1-37.1%) at three months to 3.9% (95%CI: -24.8-32.7%) at six months. Similar trends were observed for symptomatic Omicron infection. A booster dose restored protection against Omicron infection up to 51.1% (95%CI: 43.8-58.3%) and 57.3% (95%CI: 54.0-60.5%) against symptomatic infection within three months; however, this waned to 32.8% (95%CI: 16.8-48.7%) within six months. VE against severe Omicron infection following the primary course was 63.6% (95%CI: 57.5-69.7%) at three months, decreased to 49% (95%CI: 35.7-63.4%) within six months, and increased to 86% after the first or second booster dose.

Keywords: COVID-19; COVID-19 vaccines; Omicron; booster vaccination; vaccine effectiveness.

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Conflict of interest statement

H.S.M. is an investigator on vaccine trials sponsored by the GSK group of companies, Pfizer, Sanofi, and Merck. H.S.M.’s, H.M.’s, B.W.’s, M.M.’s and P.H.A.’s institution receives funding for investigator-led studies from industry, including Pfizer and Sanofi Pasteur; H.S.M., H.M., B.W., M.M. and P.H.A. receive no personal payments from industry. D.D.P.-T. and Z.Y.M.Y. declare no conflict of interest.

Figures

Figure 1
Figure 1
PRISMA flow diagram for study selection.
Figure 2
Figure 2
VE estimates against SARS-CoV-2 infection of the Omicron variant after the primary course, by vaccine types and time intervals.
Figure 3
Figure 3
VE estimates against symptomatic Omicron infection after the primary course, by vaccine types and time intervals.
Figure 4
Figure 4
Scatterplot of VE against symptomatic Omicron infection plotted according to time from the primary vaccination.
Figure 5
Figure 5
VE estimates against severe COVID-19 due to Omicron infection after the primary course by vaccine types and time intervals.
Figure 6
Figure 6
VE estimates against SARS-CoV-2 infection of the Omicron variant after one booster dose by vaccine types and time intervals.
Figure 7
Figure 7
VE estimates against symptomatic Omicron infection after one booster dose by vaccine types and time intervals.
Figure 8
Figure 8
VE estimates against severe COVID-19 due to Omicron infection after one booster dose by vaccine types and time intervals.

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