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Effectiveness of recombinant zoster vaccine against herpes zoster and postherpetic neuralgia: a systematic review and meta-analysis of post-licensure observational studies
Journal article   Open access   Peer reviewed

Effectiveness of recombinant zoster vaccine against herpes zoster and postherpetic neuralgia: a systematic review and meta-analysis of post-licensure observational studies

James F. Mbinta, Prosper Mandela A. Awuni, Sumayya T. Muhammed Basheer, Hana Kishi Generao, Aliitasi Su'a-Tavila, Steve Bowe, Andrew Harrison, Andrew Sporle, Nigel French and Colin R. Simpson
Vaccine, Vol.88, 128842
17/06/2026
Handle:
https://hdl.handle.net/10523/51526

Abstract

Herpes zoster Recombinant zoster vaccine Vaccine effectiveness
Background: Herpes zoster causes substantial morbidity in older and immunocompromised adults. The recombinant zoster vaccine is preferentially recommended, but policy decisions increasingly require real-world evidence on effectiveness across diverse populations, dosing patterns, and potential waning of protection over time. Methods: We conducted a systematic review and meta-analysis of observational studies (cohort and case-control) assessing recombinant zoster vaccine effectiveness among adults (≥18 years). Analytical observational studies published in any language between Jan 1, 2017, and Oct 31, 2025, were eligible. Methodological quality was assessed using the Joanna Briggs Institute standardised critical appraisal instruments. This study is registered on PROSPERO (CRD420251266323). Findings: A vaccine effectiveness of 80·0% (95% Confidence Intervals [CI]: 74·1-84·5) was found for immunocompetent adults and 64·3% (95 CI: 61·4-67·0) for immunocompromised adults. Vaccine effectiveness after four years was 73·0% (68·0-76·0). For people with autoimmune diseases, vaccine effectiveness was 66·2%, 95% CI 62·7-69·5). Similar vaccine effectiveness was found for adults with diabetes (66·6%, 41·8-80·9), liver disease (62·7%, 50·4-72·0), and older adults (75·1% among ≥80 years). Pooled vaccine effectiveness for postherpetic neuralgia for the immunocompetent population was 84·7% (95% CI 60·9-94·0) and for immunocompromised populations was 38·7% (95% CI 19·1-53·5). Subgroup and complication estimates were based on fewer studies and, where evidence was sparse or outcome definitions varied across datasets, should be interpreted as exploratory. Substantial heterogeneity (I2 ≥ 75%) was observed in 59% of the meta-analyses. Conclusion: For all at-risk groups, the recombinant zoster vaccine provides sustained clinically meaningful real-world benefit in preventing herpes zoster. Evidence for protection against complications and in some subgroups is supportive but limited, particularly where estimates are based on few studies or variable outcome definitions.
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Published (Version of record) Open Access CC BY V4.0
url
https://doi.org/10.1016/j.vaccine.2026.128842View
Published (Version of record) Open CC BY V4.0

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