DSpace Repository

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

Show simple item record

dc.contributor.author Chinchai T.
dc.contributor.author Chirathaworn C.
dc.contributor.author Praianantathavorn K.
dc.contributor.author Theamboonlers A.
dc.contributor.author Hutagalung Y.
dc.contributor.author Hans L. B.P.
dc.contributor.author Thantiworasit P.
dc.contributor.author Poovorawan Y.
dc.date.accessioned 2021-04-05T04:33:41Z
dc.date.available 2021-04-05T04:33:41Z
dc.date.issued 2009
dc.identifier.issn 8828245
dc.identifier.other 2-s2.0-65249109726
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/15354
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-65249109726&doi=10.1089%2fvim.2008.0087&partnerID=40&md5=334bda8c9a5372f2d95ca6ebc08e9088
dc.description.abstract Eighty-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.subject alanine aminotransferase
dc.subject aspartate aminotransferase
dc.subject gamma interferon
dc.subject hepatitis B antibody
dc.subject recombinant hepatitis B vaccine
dc.subject gamma interferon
dc.subject hepatitis B antibody
dc.subject hepatitis B vaccine
dc.subject adult
dc.subject alanine aminotransferase blood level
dc.subject antibody blood level
dc.subject antibody titer
dc.subject article
dc.subject aspartate aminotransferase blood level
dc.subject cellular immunity
dc.subject cytokine production
dc.subject enzyme linked immunospot assay
dc.subject female
dc.subject hepatitis B
dc.subject Hepatitis B virus
dc.subject high risk population
dc.subject human
dc.subject human cell
dc.subject humoral immunity
dc.subject immunological memory
dc.subject major clinical study
dc.subject male
dc.subject serology
dc.subject Thailand
dc.subject adolescent
dc.subject blood
dc.subject hepatitis B
dc.subject immunoassay
dc.subject immunology
dc.subject secretion
dc.subject T lymphocyte
dc.subject Hepatitis B virus
dc.subject Adolescent
dc.subject Hepatitis B
dc.subject Hepatitis B Antibodies
dc.subject Hepatitis B Vaccines
dc.subject Humans
dc.subject Immunoassay
dc.subject Immunologic Memory
dc.subject Interferon-gamma
dc.subject T-Lymphocytes
dc.subject Thailand
dc.subject Young Adult
dc.title Long-term humoral and cellular immune response to hepatitis B vaccine in high-risk children 18-20 years after neonatal immunization
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Viral Immunology. Vol 22, No.2 (2009), p.125-130
dc.identifier.doi 10.1089/vim.2008.0087


Files in this item

Files Size Format View

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Advanced Search

Browse

My Account

Statistics