Recommendations of the Advisory Committee on Immunization Practices for Use of Herpes Zoster Vaccines
- PMID: 29370152
- PMCID: PMC5812314
- DOI: 10.15585/mmwr.mm6703a5
Recommendations of the Advisory Committee on Immunization Practices for Use of Herpes Zoster Vaccines
Abstract
On October 20, 2017, Zoster Vaccine Recombinant, Adjuvanted (Shingrix, GlaxoSmithKline, [GSK] Research Triangle Park, North Carolina), a 2-dose, subunit vaccine containing recombinant glycoprotein E in combination with a novel adjuvant (AS01B), was approved by the Food and Drug Administration for the prevention of herpes zoster in adults aged ≥50 years. The vaccine consists of 2 doses (0.5 mL each), administered intramuscularly, 2-6 months apart (1). On October 25, 2017, the Advisory Committee on Immunization Practices (ACIP) recommended the recombinant zoster vaccine (RZV) for use in immunocompetent adults aged ≥50 years.
Conflict of interest statement
No conflicts of interest were reported.
References
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- Food and Drug Administration. Shingrix [package insert]. Silver Spring, MD: US Department of Health and Human Services, Food and Drug Administration; 2017. https://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedPr...
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