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Sökning: WFRF:(Plassmann Georg) > (2016) > Long-term immunogen...

Long-term immunogenicity and safety of an investigational herpes zoster subunit vaccine in older adults

Chlibek, Roman (författare)
Univ Def, Fac Mil Hlth Sci, Hradec Kralove, Czech Republic.
Pauksens, Karlis (författare)
Uppsala universitet,Infektionssjukdomar
Rombo, Lars (författare)
Uppsala universitet,Centrum för klinisk forskning i Sörmland (CKFD),Karolinska Univ Hosp, Dept Med, Stockholm, Sweden.
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van Rijckevorsel, Gini (författare)
Publ Hlth Serv Amsterdam, Dept Infect Dis, Amsterdam, Netherlands.
Richardus, Jan H. (författare)
Municipal Publ Hlth Serv Rotterdam Rijnmond, Rotterdam, Netherlands.
Plassmann, Georg (författare)
Unterfrintroper Hausarztzentrum, Essen, Germany.
Schwarz, Tino F. (författare)
Stiftung juliusspital, Cent Lab, Wurzburg, Germany.;Stiftung juliusspital, Vaccinat Ctr, Wurzburg, Germany.
Catteau, Gregory (författare)
GSK Vaccines, Wavre, Belgium.
Lal, Himal (författare)
GSK Vaccines, King Of Prussia, PA USA.
Heineman, Thomas C. (författare)
GSK Vaccines, King Of Prussia, PA USA.
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Univ Def, Fac Mil Hlth Sci, Hradec Kralove, Czech Republic Infektionssjukdomar (creator_code:org_t)
Elsevier BV, 2016
2016
Engelska.
Ingår i: Vaccine. - : Elsevier BV. - 0264-410X .- 1873-2518. ; 34:6, s. 863-868
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background: An investigational subunit vaccine containing the varicella-zoster virus (VZV) glycoprotein E (gE) and the AS01(B) adjuvant system is being evaluated for the prevention of herpes zoster (HZ) in older adults. A phase II trial evaluating different formulations of this vaccine (containing 25 mu g, 50 mu g, or 100 mu g gE) was conducted in adults >= 60 years of age and showed that all formulations elicited robust cellular and humoral immune responses for up to 3 years after vaccination. In this follow-up study in subjects who received two doses of the 50 mu g gE/AS01(B) formulation (HZ/su), we assessed the persistence of the immune responses for up to 6 years after vaccination. Methods: This phase II, open-label, multicenter, single-group trial conducted in the Czech Republic, Germany, Sweden, and the Netherlands followed 129 subjects who had received two doses (2 months apart) of HZ/su during the initial trial. Vaccine-induced immune responses (frequencies of gE-specific CD4(+) T cells expressing >= 2 activation markers and serum anti-gE antibody concentrations) were evaluated at 48, 60, and 72 months after the first HZ/su dose. Results: Six years after vaccination with HZ/su, gE-specific cell-mediated immune responses and anti-gE antibody concentrations had decreased by 20-25% from month 36, but remained higher than the prevaccination values. At month 72, the gE-specific cell-mediated immune response was 3.8 times higher than the prevaccination value (477.3 vs. 119.4 activated gE-specific CD4(+) T cells per 10(6) cells), and the anti-gE antibody concentration was 7.3 times higher than the prevaccination value (8159.0 vs. 1121.3 mIU/mL). No vaccine-related serious adverse events were reported between months 36 and 72. Conclusions: gE-specific cellular and humoral immune responses persisted for 6 years after two-dose vaccination with HZ/su in healthy older adults. No safety concerns were identified.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)

Nyckelord

Varicella-zoster virus
Glycoprotein E
Subunit vaccine
lmmunogenicity
Persistence

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