Antibody persistence 2 and 3 years after booster vaccination of adolescents with recombinant acellular pertussis monovalent aP gen or combined TdaP gen vaccines

Recombinant pertussis vaccines inducing long-lasting immune responses could help to control the rise in pertussis. We here report on persisting antibody responses 2 and 3 years after booster vaccination with a new generation recombinant acellular pertussis vaccine. Participants of a phase 2/3 random...

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Veröffentlicht in:EClinicalMedicine 2021-07, Vol.37, p.100976
Hauptverfasser: Pitisuttithum, Punnee, Dhitavat, Jittima, Sirivichayakul, Chukiat, Pitisuthitham, Arom, Sabmee, Yupa, Chinwangso, Pailinrut, Kerdsomboon, Chawanee, Fortuna, Librada, Spiegel, Jane, Chauhan, Mukesh, Poredi, Indrajeet Kumar, van den Biggelaar, Anita H J, Wijagkanalan, Wassana, Viviani, Simonetta, Mansouri, Souad, Pham, Hong Thai
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Sprache:eng
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Zusammenfassung:Recombinant pertussis vaccines inducing long-lasting immune responses could help to control the rise in pertussis. We here report on persisting antibody responses 2 and 3 years after booster vaccination with a new generation recombinant acellular pertussis vaccine. Participants of a phase 2/3 randomised-controlled clinical trial with a monovalent pertussis vaccine containing genetically inactivated pertussis toxin (aP ) or its tetanus and diphtheria toxoids combination (TdaP ), or a chemically detoxified comparator vaccine (Tdap ), (originally conducted between July and August 2015) were invited to participate in observational studies of persisting antibody responses 2 and 3 years after vaccination. Serum IgG against pertussis toxin (PT-IgG) and filamentous hemagglutinin (FHA-IgG) were assessed by ELISA, and PT-neutralising antibodies (PT-Nab) by Chinese Hamster Ovary cell assay. Waning of antibodies stabilised in aP and TdaP vaccinees 2 and 3 years after vaccination. Three years post-vaccination PT-neutralising antibodies remained 4·6-fold (95% Confidence Interval (CI) 2·6-8·1) and 3·7-fold (95% CI 2·2-6·1) higher, PT-IgG antibodies 3·0-fold (95% CI 2·2-4·1) and 2·5-fold (95% CI 1·9-3·3) higher, and FHA-IgG antibodies 1·8-fold (95% CI 1·3-2·5) and 1·6-fold (95% CI 1·2-2·1) higher than baseline in aP and TdaP recipients, respectively. In the Tdap group, PT-neutralising and PT-IgG and FHA-IgG antibodies were back at baseline levels 2 years post-vaccination. Three years post-vaccination seroconversion rates for PT-neutralising antibodies were 65·0% (95% CI 44·1-85·9) and 55·0% (95% CI 33·2-76·8) in aP and TdaP recipients, respectively. Considering the persistence of elevated antibody responses 3 years post-booster vaccination, genetically detoxified monovalent aP and TdaP vaccines can be expected to induce longer-lasting protection than chemically inactivated Tdap vaccines. BioNet-Asia.
ISSN:2589-5370