Publication: A single dose of vero cell-derived Japanese encephalitis (JE) vaccine (Ixiaro) effectively boosts immunity in travelers primed with mouse brain-derived JE vaccines.
dc.contributor.author | Elina O. Erra | en_US |
dc.contributor.author | Helena Hervius Askling | en_US |
dc.contributor.author | Lars Rombo | en_US |
dc.contributor.author | Jukka Riutta | en_US |
dc.contributor.author | Sirkka Vene | en_US |
dc.contributor.author | Sutee Yoksan | en_US |
dc.contributor.author | Lars Lindquist | en_US |
dc.contributor.author | Pakkanen, Sari H. | en_US |
dc.contributor.author | Eili Huhtamo | en_US |
dc.contributor.author | Olli Vapalahti | en_US |
dc.contributor.author | Anu Kantele | en_US |
dc.contributor.other | Mahidol University. Faculty of Medicine. Haartman Institute | en_US |
dc.contributor.other | Mahidol University. Institute of Molecular Bioscience | en_US |
dc.date.accessioned | 2015-06-13T07:26:19Z | |
dc.date.accessioned | 2017-04-25T03:40:56Z | |
dc.date.available | 2015-06-13T07:26:19Z | |
dc.date.available | 2017-04-25T03:40:56Z | |
dc.date.created | 2015-06-13 | |
dc.date.issued | 2012-06 | |
dc.description.abstract | BACKGROUND: A significant part of the world population lives in areas with endemic Japanese encephalitis (JE). For travelers from nonendemic countries, Vero cell-derived vaccine (JE-VC; Ixiaro) has replaced traditional mouse brain-derived vaccines (JE-MB) associated with safety concerns. The 2 vaccines are derived from different viral strains: JE-VC from the SA14-14-2 strain and JE-MB from the Nakayama strain. No data exist regarding whether JE-VC can be used to boost immunity after a primary series of JE-MB; therefore, a primary series of JE-VC has been recommended to all travelers regardless of previous vaccination history. METHODS: One hundred twenty travelers were divided into 4 groups: Volunteers with no prior JE vaccination received primary immunization with (group 1) JE-MB or (group 2) JE-VC, and those primed with JE-MB received a single booster dose of (group 3) JE-MB or (group 4) JE-VC. Immune responses were tested before and 4-8 weeks after vaccination using plaque reduction neutralization test (PRNT) against both vaccine strains. RESULTS: In vaccine-naive travelers, the vaccination response rate for test strains Nakayama and SA14-14-2 was 100% and 87% after primary vaccination with JE-MB and 87% and 94% after JE-VC, respectively. Antibody levels depended on the target virus, with higher titers against homologous than heterologous PRNT(50) target strain (P < .001). In travelers primed with JE-MB, vaccination response rates were 91% and 91%, and 98% and 95% after a booster dose of JE-MB or JE-VC, respectively. Subgroup analysis revealed that a higher proportion of primed (98%/95%) than nonprimed (39%/42%) volunteers responded to a single dose of JE-VC (P < .001). CONCLUSIONS: A single dose of JE-VC effectively boosted immunity in JE-MB-primed travelers. Current recommendations should be reevaluated. CLINICAL TRIALS REGISTRATION: NCT01386827. | en_US |
dc.identifier.citation | Clinical Infectious Diseases. Vol.55, No.6 (2012), 825-834 | en_US |
dc.identifier.doi | 10.1093/cid/cis542. | |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/1822 | |
dc.language.iso | eng | en_US |
dc.rights | Mahidol University | en_US |
dc.rights.holder | Oxford University Press | |
dc.subject | Single Dose | en_US |
dc.subject | Vero Cell–Derived | en_US |
dc.subject | Japanese | en_US |
dc.subject | (JE) | en_US |
dc.subject | Vaccine | en_US |
dc.subject | (Ixiaro) | en_US |
dc.subject | Effectively Boosts Immunity | en_US |
dc.subject | Mouse Brain–Derived | en_US |
dc.subject | Vaccines | en_US |
dc.subject | Open Access article | en_US |
dc.title | A single dose of vero cell-derived Japanese encephalitis (JE) vaccine (Ixiaro) effectively boosts immunity in travelers primed with mouse brain-derived JE vaccines. | en_US |
dc.type | Article | en_US |
dcterms.dateAccepted | 2012-04-19 | |
dspace.entity.type | Publication | |
mods.location.url | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423932/pdf/cis542.pdf |