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Immune Responses to a Recombinant Glycoprotein E Herpes Zoster Vaccine in Adults Aged 50 Years or Older
AL. Cunningham, TC. Heineman, H. Lal, O. Godeaux, R. Chlibek, SJ. Hwang, JE. McElhaney, T. Vesikari, C. Andrews, WS. Choi, M. Esen, H. Ikematsu, MK. Choma, K. Pauksens, S. Ravault, B. Salaun, TF. Schwarz, J. Smetana, CV. Abeele, P. Van den Steen,...
Jazyk angličtina Země Spojené státy americké
Typ dokumentu klinické zkoušky, fáze III, časopisecké články, randomizované kontrolované studie, práce podpořená grantem
NLK
Free Medical Journals
od 1997 do Před 1 rokem
Open Access Digital Library
od 1997-04-01
PubMed
29529222
DOI
10.1093/infdis/jiy095
Knihovny.cz E-zdroje
- MeSH
- adjuvancia imunologická farmakologie MeSH
- buněčná imunita imunologie MeSH
- CD4-pozitivní T-lymfocyty MeSH
- herpes zoster imunologie MeSH
- humorální imunita imunologie MeSH
- imunogenicita vakcíny imunologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- lipid A analogy a deriváty farmakologie MeSH
- proteiny virového obalu imunologie MeSH
- protilátky virové imunologie MeSH
- saponiny farmakologie MeSH
- senioři MeSH
- subjednotkové vakcíny imunologie MeSH
- vakcína proti pásovému oparu imunologie MeSH
- vakcinace metody MeSH
- virus varicella zoster imunologie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze III MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
Background: The herpes zoster subunit vaccine (HZ/su), consisting of varicella-zoster virus glycoprotein E (gE) and AS01B Adjuvant System, was highly efficacious in preventing herpes zoster in the ZOE-50 and ZOE-70 trials. We present immunogenicity results from those trials. Methods: Participants (ZOE-50: ≥50; ZOE-70: ≥70 years of age) received 2 doses of HZ/su or placebo, 2 months apart. Serum anti-gE antibodies and CD4 T cells expressing ≥2 of 4 activation markers assessed (CD42+) after stimulation with gE-peptides were measured in subcohorts for humoral (n = 3293) and cell-mediated (n = 466) immunogenicity. Results: After vaccination, 97.8% of HZ/su and 2.0% of placebo recipients showed a humoral response. Geometric mean anti-gE antibody concentrations increased 39.1-fold and 8.3-fold over baseline in HZ/su recipients at 1 and 36 months post-dose 2, respectively. A gE-specific CD42+ T-cell response was shown in 93.3% of HZ/su and 0% of placebo recipients. Median CD42+ T-cell frequencies increased 24.6-fold (1 month) and 7.9-fold (36 months) over baseline in HZ/su recipients and remained ≥5.6-fold above baseline in all age groups at 36 months. The proportion of CD4 T cells expressing all 4 activation markers increased over time in all age groups. Conclusions: Most HZ/su recipients developed robust immune responses persisting for 3 years following vaccination. Clinical Trials Registration: NCT01165177; NCT01165229.
Central Laboratory and Vaccination Centre Klinikum Würzburg Mitte Standort Juliusspital Germany
Department of Infectious Diseases Uppsala University Hospital Sweden
Diagnostics Research Group San Antonio Texas
Faculty of Military Health Sciences University of Defense Hradec Kralove Czech Republic
Federal University of Sao Paulo Brazil
GSK King of Prussia Pennsylvania
Health Sciences North Research Institute Sudbury Ontario Canada
Institute of Tropical Medicine University Clinic of Tuebingen Germany
Japan Physicians Association Kanda Chiyoda ku Tokyo
The Westmead Institute for Medical Research University of Sydney Australia
Citace poskytuje Crossref.org
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