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dc.contributor.authorNuntisa Chotirosniramiten_US
dc.contributor.authorPatcharaphan Sugandhavesaen_US
dc.contributor.authorLinda Aurpibulen_US
dc.contributor.authorSunida Thetketen_US
dc.contributor.authorNatthapol Kosashunhananen_US
dc.contributor.authorTaweewat Supindhamen_US
dc.contributor.authorPanuwat Wongkulaben_US
dc.contributor.authorQuanhathai Kaewpoowaten_US
dc.contributor.authorKanokporn Chaiklangen_US
dc.contributor.authorOranitcha Kaewthipen_US
dc.contributor.authorPiyathida Sroysuwanen_US
dc.contributor.authorAntika Wongthaneeen_US
dc.contributor.authorHatairat Lerdsamranen_US
dc.contributor.authorPilaipan Puthavathanaen_US
dc.contributor.authorKhuanchai Suparatpinyoen_US
dc.date.accessioned2018-09-04T06:06:49Z-
dc.date.available2018-09-04T06:06:49Z-
dc.date.issued2012-12-01en_US
dc.identifier.issn2164554Xen_US
dc.identifier.issn21645515en_US
dc.identifier.other2-s2.0-84872231259en_US
dc.identifier.other10.4161/hv.21820en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84872231259&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/51710-
dc.description.abstractBackground: In late 2009, the Thai Ministry of Public Health provided two million doses of the monovalent pandemic influenza H1N1 2009 vaccine (Panenza® Sanofi Pasteur), which was the only vaccine formulation available in Thailand, to persons at risk of more severe manifestations of the disease including HIV infection. Several studies have shown poorer immune responses to the 2009 H1N1 vaccines in HIV-infected individuals. There are limited data in this population in resource-limited countries. Results: At day 28 post-vaccination, seroconversion was found in 32.0% (95% CI 24.5-40.2) of the HIV-infected group and 35.0% (95% CI 15.4-59.2) of the healthy controls (p = 0.79). Seroprotection rate was observed in 33.3% (95% CI 25.8-41.6) and 35.0% (95% CI 15.4-59.2) of the HIV-infected group and the control group, respectively (p = 0.88). Among HIV-infected participants, the strongest factor associated with vaccine response was age 42 y or younger (p = 0.05). Methods: We evaluated the immunogenicity of a single, 15μg/0.5ml dose of a monovalent, non-adjuvanted 2009 H1N1 vaccine in 150 HIV-infected Thai adults and 20 healthy controls. Immunogenicity was measured by hemagglutination inhibition assay (HI) at baseline and 28 d after vaccination. Seroconversion was defined as 1) pre-vaccination HI titer < 1:10 and post-vaccination HI titer ≥ 1:40, or 2) pre-vaccination HI titer ≥ 1:10 and a minimum of 4-fold rise in post-vaccination HI titer. Seroprotection was defined as a post-vaccination HI titer of ≥ 1:40. Conclusions: A low seroconversion rate to the 2009 H1N1 vaccine in both study groups, corresponding with data from trials in the region, may suggest that the vaccine used in our study is not very immunogenic. Further studies on different vaccines, dosing, adjuvants, or schedule strategies may be needed to achieve effective immunization in HIV-infected population. © 2012 Landes Bioscience.en_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleImmune response to 2009 H1N1 vaccine in HIV-infected adults in Northern Thailanden_US
dc.typeJournalen_US
article.title.sourcetitleHuman Vaccines and Immunotherapeuticsen_US
article.volume8en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsMahidol Universityen_US
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