Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/15354
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dc.contributor.authorChinchai T.
dc.contributor.authorChirathaworn C.
dc.contributor.authorPraianantathavorn K.
dc.contributor.authorTheamboonlers A.
dc.contributor.authorHutagalung Y.
dc.contributor.authorHans L. B.P.
dc.contributor.authorThantiworasit P.
dc.contributor.authorPoovorawan Y.
dc.date.accessioned2021-04-05T04:33:41Z-
dc.date.available2021-04-05T04:33:41Z-
dc.date.issued2009
dc.identifier.issn8828245
dc.identifier.other2-s2.0-65249109726
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/15354-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-65249109726&doi=10.1089%2fvim.2008.0087&partnerID=40&md5=334bda8c9a5372f2d95ca6ebc08e9088
dc.description.abstractEighty-seven high-risk individuals in Thailand who had received a complete course of recombinant HBV vaccine 18-20 y ago were investigated with regard to their immunological memory. To evaluate humoral immunity, anti-HBs antibody titers were measured. Cellular immunity was determined by ELISPOT to detect HBV-specific IFN-γ-producing cells. Overall 83.9% of participants developed circulating anti-HBs (titer ≥ mIU/mL) and 58.6% were seroprotected (titer ≥10 mIU/mL). As for cellular immunity, 50.6% were positive on ELISPOT. Moreover, there was no correlation between the level of anti-HBs and positive ELISPOT results. However, the majority of participants (81.8%) who were positive for IFN-γ-producing cells were seropositive, but only 50% of seropositive participants were ELISPOT-positive. Thus, 18-20 y after immunization, it appears that a second booster dose should be considered, especially in high-risk groups. © Copyright 2009, Mary Ann Liebert, Inc.
dc.subjectalanine aminotransferase
dc.subjectaspartate aminotransferase
dc.subjectgamma interferon
dc.subjecthepatitis B antibody
dc.subjectrecombinant hepatitis B vaccine
dc.subjectgamma interferon
dc.subjecthepatitis B antibody
dc.subjecthepatitis B vaccine
dc.subjectadult
dc.subjectalanine aminotransferase blood level
dc.subjectantibody blood level
dc.subjectantibody titer
dc.subjectarticle
dc.subjectaspartate aminotransferase blood level
dc.subjectcellular immunity
dc.subjectcytokine production
dc.subjectenzyme linked immunospot assay
dc.subjectfemale
dc.subjecthepatitis B
dc.subjectHepatitis B virus
dc.subjecthigh risk population
dc.subjecthuman
dc.subjecthuman cell
dc.subjecthumoral immunity
dc.subjectimmunological memory
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectserology
dc.subjectThailand
dc.subjectadolescent
dc.subjectblood
dc.subjecthepatitis B
dc.subjectimmunoassay
dc.subjectimmunology
dc.subjectsecretion
dc.subjectT lymphocyte
dc.subjectHepatitis B virus
dc.subjectAdolescent
dc.subjectHepatitis B
dc.subjectHepatitis B Antibodies
dc.subjectHepatitis B Vaccines
dc.subjectHumans
dc.subjectImmunoassay
dc.subjectImmunologic Memory
dc.subjectInterferon-gamma
dc.subjectT-Lymphocytes
dc.subjectThailand
dc.subjectYoung Adult
dc.titleLong-term humoral and cellular immune response to hepatitis B vaccine in high-risk children 18-20 years after neonatal immunization
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationViral Immunology. Vol 22, No.2 (2009), p.125-130
dc.identifier.doi10.1089/vim.2008.0087
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