Publication:
Long-term humoral and cellular immune response to hepatitis B vaccine in high-risk children 18-20 years after neonatal immunization

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.date.issuedBE2552
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.format.mimetypeapplication/pdf
dc.identifier.citationViral Immunology. Vol 22, No.2 (2009), p.125-130
dc.identifier.doi10.1089/vim.2008.0087
dc.identifier.issn8828245
dc.identifier.other2-s2.0-65249109726
dc.identifier.urihttps://hdl.handle.net/20.500.14740/7297
dc.rights.holderมหาวิทยาลัยศรีนครินทรวิโรฒ
dc.subject.otherAlanine aminotransferase
dc.subject.otherAspartate aminotransferase
dc.subject.otherGamma interferon
dc.subject.otherHepatitis B antibody
dc.subject.otherRecombinant hepatitis B vaccine
dc.subject.otherGamma interferon
dc.subject.otherHepatitis B antibody
dc.subject.otherHepatitis B vaccine
dc.subject.otherAdult
dc.subject.otherAlanine aminotransferase blood level
dc.subject.otherAntibody blood level
dc.subject.otherAntibody titer
dc.subject.otherArticle
dc.subject.otherAspartate aminotransferase blood level
dc.subject.otherCellular immunity
dc.subject.otherCytokine production
dc.subject.otherEnzyme linked immunospot assay
dc.subject.otherFemale
dc.subject.otherHepatitis B
dc.subject.otherHepatitis B virus
dc.subject.otherHigh risk population
dc.subject.otherHuman
dc.subject.otherHuman cell
dc.subject.otherHumoral immunity
dc.subject.otherImmunological memory
dc.subject.otherMajor clinical study
dc.subject.otherMale
dc.subject.otherSerology
dc.subject.otherThailand
dc.subject.otherAdolescent
dc.subject.otherBlood
dc.subject.otherHepatitis B
dc.subject.otherImmunoassay
dc.subject.otherImmunology
dc.subject.otherSecretion
dc.subject.otherT lymphocyte
dc.subject.otherHepatitis B virus
dc.subject.otherAdolescent
dc.subject.otherHepatitis B
dc.subject.otherHepatitis B Antibodies
dc.subject.otherHepatitis B Vaccines
dc.subject.otherHumans
dc.subject.otherImmunoassay
dc.subject.otherImmunologic Memory
dc.subject.otherInterferon-gamma
dc.subject.otherT-Lymphocytes
dc.subject.otherThailand
dc.subject.otherYoung 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
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-65249109726&doi=10.1089%2fvim.2008.0087&partnerID=40&md5=334bda8c9a5372f2d95ca6ebc08e9088

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