Immunogenicity of the Adjuvanted Recombinant Zoster Vaccine: Persistence and Anamnestic Response to Additional Doses Administered 10 Years After Primary Vaccination
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
32502272
PubMed Central
PMC8672743
DOI
10.1093/infdis/jiaa300
PII: 5851921
Knihovny.cz E-zdroje
- Klíčová slova
- adjuvanted recombinant zoster vaccine, herpes zoster, persistence of immune response, safety,
- MeSH
- adjuvancia imunologická aplikace a dávkování škodlivé účinky MeSH
- herpes zoster prevence a kontrola MeSH
- imunogenicita vakcíny * MeSH
- lidé středního věku MeSH
- lidé MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- syntetické vakcíny aplikace a dávkování škodlivé účinky imunologie MeSH
- vakcína proti pásovému oparu aplikace a dávkování škodlivé účinky MeSH
- vakcinace MeSH
- virus varicella zoster imunologie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adjuvancia imunologická MeSH
- syntetické vakcíny MeSH
- vakcína proti pásovému oparu MeSH
BACKGROUND: The adjuvanted recombinant zoster vaccine (RZV) is highly immunogenic and efficacious in adults ≥50 years of age. We evaluated (1) long-term immunogenicity of an initial 2-dose RZV schedule, by following up adults vaccinated at ≥60 years of age and by modeling, and (2) immunogenicity of 2 additional doses administered 10 years after initial vaccination. METHODS: Persistence of humoral and cell-mediated immune (CMI) responses to 2 initial RZV doses was assessed through 10 years after initial vaccination, and modeled through 20 years using a Piecewise, Power law and Fraser model. The immunogenicity and safety of 2 additional RZV doses were also evaluated. RESULTS: Seventy adults were enrolled. Ten years after initial vaccination, humoral and CMI responses were approximately 6-fold and 3.5-fold, respectively, above those before the initial vaccination levels. Predicted immune persistence through 20 years after initial vaccination was similar across the 3 models. Sixty-two participants (mean age [standard deviation], 82.6 [4.4] years) received ≥1 additional RZV dose. Strong anamnestic humoral and CMI responses were elicited by 1 additional dose, without further increases after a second additional dose. CONCLUSIONS: Immune responses to an initial 2-dose RZV course persisted for many years in older adults. Strong anamnestic immune responses can be induced by additional dosing 10 years after the initial 2-dose course. CLINICAL TRIALS REGISTRATION: NCT02735915.
Centre for Clinical Research Eskilstuna Sweden
Department of Infectious Diseases Uppsala University Hospital Uppsala Sweden
Faculty of Military Health Sciences University of Defence Hradec Kralove Czech Republic
Klinikum Wuerzburg Mitte Standort Juliusspital Wuerzburg Germany
Mithra Pharmaceuticals Flémalle Belgium
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ClinicalTrials.gov
NCT02735915