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Sökning: onr:"swepub:oai:DiVA.org:uu-280259" > Long-term immunogen...

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FältnamnIndikatorerMetadata
00004655naa a2200481 4500
001oai:DiVA.org:uu-280259
003SwePub
008160309s2016 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-2802592 URI
024a https://doi.org/10.1016/j.vaccine.2015.09.0732 DOI
040 a (SwePub)uu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Chlibek, Romanu Univ Def, Fac Mil Hlth Sci, Hradec Kralove, Czech Republic.4 aut
2451 0a Long-term immunogenicity and safety of an investigational herpes zoster subunit vaccine in older adults
264 1b Elsevier BV,c 2016
338 a electronic2 rdacarrier
520 a 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.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Immunologi inom det medicinska området0 (SwePub)301102 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Immunology in the medical area0 (SwePub)301102 hsv//eng
653 a Varicella-zoster virus
653 a Glycoprotein E
653 a Subunit vaccine
653 a lmmunogenicity
653 a Persistence
700a Pauksens, Karlisu Uppsala universitet,Infektionssjukdomar4 aut0 (Swepub:uu)karlpauk
700a Rombo, Larsu Uppsala universitet,Centrum för klinisk forskning i Sörmland (CKFD),Karolinska Univ Hosp, Dept Med, Stockholm, Sweden.4 aut0 (Swepub:uu)larra728
700a van Rijckevorsel, Giniu Publ Hlth Serv Amsterdam, Dept Infect Dis, Amsterdam, Netherlands.4 aut
700a Richardus, Jan H.u Municipal Publ Hlth Serv Rotterdam Rijnmond, Rotterdam, Netherlands.4 aut
700a Plassmann, Georgu Unterfrintroper Hausarztzentrum, Essen, Germany.4 aut
700a Schwarz, Tino F.u Stiftung juliusspital, Cent Lab, Wurzburg, Germany.;Stiftung juliusspital, Vaccinat Ctr, Wurzburg, Germany.4 aut
700a Catteau, Gregoryu GSK Vaccines, Wavre, Belgium.4 aut
700a Lal, Himalu GSK Vaccines, King Of Prussia, PA USA.4 aut
700a Heineman, Thomas C.u GSK Vaccines, King Of Prussia, PA USA.4 aut
710a Univ Def, Fac Mil Hlth Sci, Hradec Kralove, Czech Republic.b Infektionssjukdomar4 org
773t Vaccined : Elsevier BVg 34:6, s. 863-868q 34:6<863-868x 0264-410Xx 1873-2518
856u https://doi.org/10.1016/j.vaccine.2015.09.073y Fulltext
856u https://uu.diva-portal.org/smash/get/diva2:910457/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print
856u https://doi.org/10.1016/j.vaccine.2015.09.073
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-280259
8564 8u https://doi.org/10.1016/j.vaccine.2015.09.073

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