What is the efficacy of Shingrix (zoster vaccine recombinant) after 1 dose in preventing shingles, particularly in older adults or those with potential immunocompromising conditions?

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Efficacy of Shingrix After 1 Dose

A single dose of Shingrix provides 56.9% effectiveness against herpes zoster, which is substantially lower than the 70.1% effectiveness achieved with the complete 2-dose series—making completion of both doses essential for optimal protection. 1

Single-Dose Effectiveness Data

  • The largest real-world effectiveness study in Medicare beneficiaries aged >65 years demonstrated that one dose of Shingrix provides 56.9% (95% CI, 55.0-58.8) vaccine effectiveness against herpes zoster 1

  • This single-dose effectiveness is significantly inferior to the 2-dose series effectiveness of 70.1% (95% CI, 68.6-71.5), representing a meaningful reduction in protection 1

  • These real-world effectiveness estimates are notably lower than the >90% efficacy demonstrated in clinical trials (97.2% in adults ≥50 years, 89.8% in adults ≥70 years), likely due to differences in outcome specificity and real-world conditions versus controlled trial settings 2, 1

Clinical Trial Data on Incomplete Vaccination

  • The pivotal ZOE-50 and ZOE-70 trials were designed to evaluate the 2-dose regimen (administered at 0 and 2 months), and efficacy data for a single dose was not a primary endpoint in these registration studies 2

  • The FDA label explicitly states that Shingrix is administered as a two-dose series, with the second dose given 2 to 6 months after the first dose, and does not provide efficacy claims for single-dose protection 3, 2

Importance of Second-Dose Completion

  • Real-world data from October 2017 to September 2019 showed that among 7,097,441 first doses administered, only 70% of recipients completed the two-dose series within 6 months, and 80% within 12 months—indicating substantial dropout rates 4

  • The second dose is critical for achieving the high level of protection (>90% in trials, 70% in real-world settings) that makes Shingrix superior to the older live-attenuated vaccine Zostavax 3, 1

  • Second doses administered beyond the recommended 6-month window (at ≥180 days) maintain full effectiveness without impairment, so delayed completion is preferable to remaining with only one dose 1

Practical Implications

  • For immunocompetent adults aged ≥50 years, the second dose should be administered 2-6 months after the first dose, with a minimum interval of 4 weeks 3

  • For immunocompromised adults aged ≥18 years, a shortened schedule with the second dose at 1-2 months is recommended to provide earlier protection in this higher-risk population 3, 5

  • Patients who have received only one dose should be strongly counseled to complete the series, as single-dose protection of 56.9% leaves them substantially vulnerable compared to the 70.1% protection from two doses 1

Common Pitfall to Avoid

  • Do not assume that one dose provides adequate protection—the 13.2 percentage point difference in effectiveness between one and two doses (56.9% vs 70.1%) translates to a meaningful increase in herpes zoster risk for incompletely vaccinated individuals 1

  • The high reactogenicity of Shingrix (injection-site reactions in 9.5%, systemic symptoms in 11.4%) may deter some patients from returning for the second dose, but these transient side effects should not prevent series completion given the substantial efficacy benefit 3, 6

References

Research

Recombinant Zoster Vaccine (Shingrix): Real-World Effectiveness in the First 2 Years Post-Licensure.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2021

Guideline

SHINGRIX Vaccination Schedule for Adults

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Special Indications for Shingrix Under Age 50

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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