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Immunogenicity and tolerability after two doses of non-adjuvanted, whole-virion pandemic influenza A (H1N1) vaccine in HIV-infected individuals.

Identifieur interne : 000C87 ( PubMed/Corpus ); précédent : 000C86; suivant : 000C88

Immunogenicity and tolerability after two doses of non-adjuvanted, whole-virion pandemic influenza A (H1N1) vaccine in HIV-infected individuals.

Auteurs : Heimo Lagler ; Katharina Grabmeier-Pfistershammer ; Veronique Touzeau-Römer ; Selma Tobudic ; Michael Ramharter ; Judith Wenisch ; Guido Andrés Gualdoni ; Monika Redlberger-Fritz ; Theresia Popow-Kraupp ; Armin Rieger ; Heinz Burgmann

Source :

RBID : pubmed:22629330

English descriptors

Abstract

During the influenza pandemic of 2009/10, the whole-virion, Vero-cell-derived, inactivated, pandemic influenza A (H1N1) vaccine Celvapan® (Baxter) was used in Austria. Celvapan® is adjuvant-free and was the only such vaccine at that time in Europe. The objective of this observational, non-interventional, prospective single-center study was to evaluate the immunogenicity and tolerability of two intramuscular doses of this novel vaccine in HIV-positive individuals.

DOI: 10.1371/journal.pone.0036773
PubMed: 22629330

Links to Exploration step

pubmed:22629330

Le document en format XML

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<term>HIV Infections</term>
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<div type="abstract" xml:lang="en">During the influenza pandemic of 2009/10, the whole-virion, Vero-cell-derived, inactivated, pandemic influenza A (H1N1) vaccine Celvapan® (Baxter) was used in Austria. Celvapan® is adjuvant-free and was the only such vaccine at that time in Europe. The objective of this observational, non-interventional, prospective single-center study was to evaluate the immunogenicity and tolerability of two intramuscular doses of this novel vaccine in HIV-positive individuals.</div>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">During the influenza pandemic of 2009/10, the whole-virion, Vero-cell-derived, inactivated, pandemic influenza A (H1N1) vaccine Celvapan® (Baxter) was used in Austria. Celvapan® is adjuvant-free and was the only such vaccine at that time in Europe. The objective of this observational, non-interventional, prospective single-center study was to evaluate the immunogenicity and tolerability of two intramuscular doses of this novel vaccine in HIV-positive individuals.</AbstractText>
<AbstractText Label="METHODS AND FINDINGS" NlmCategory="RESULTS">A standard hemagglutination inhibition (HAI) assay was used for evaluation of the seroconversion rate and seroprotection against the pandemic H1N1 strain. In addition, H1N1-specific IgG antibodies were measured using a recently developed ELISA and compared with the HAI results. Tolerability of vaccination was evaluated up to one month after the second dose. A total of 79 HIV-infected adults with an indication for H1N1 vaccination were evaluated. At baseline, 55 of the 79 participants had an HAI titer ≥1:40 and two patients showed a positive IgG ELISA. The seroconversion rate was 31% after the first vaccination, increasing to 41% after the second; the corresponding seroprotection rates were 92% and 83% respectively. ELISA IgG levels were positive in 25% after the first vaccination and in 37% after the second. Among the participants with baseline HAI titers <1:40, 63% seroconverted. Young age was clearly associated with lower HAI titers at baseline and with higher seroconversion rates, whereas none of the seven patients >60 years of age had a baseline HAI titer <1:40 or seroconverted after vaccination. The vaccine was well tolerated.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">The non-adjuvanted pandemic influenza A (H1N1) vaccine was well tolerated and induced a measurable immune response in a sample of HIV-infected individuals.</AbstractText>
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<Citation>PLoS One. 2011;6(11):e27214</Citation>
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<Citation>Dev Biol (Basel). 2003;115:63-73</Citation>
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