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KMID : 0191120160310091383
Journal of Korean Medical Science
2016 Volume.31 No. 9 p.1383 ~ p.1391
The Immunogenicity and Safety of a Combined DTaP-IPV//Hib Vaccine Compared with Individual DTaP-IPV and Hib (PRP~T) Vaccines: a Randomized Clinical Trial in South Korean Infants
Kang Jin-Han

Lee Hoan-Jong
Kim Kyung-Hyo
Oh Sung-Hee
Cha Sung-Ho
Lee Jin
Kim Nam-Hee
Eun Byung-Wook
Kim Chang-Hwi
Hong Young-Jin
Kim Hyun-Hee
Lee Kyung-Yil
Kim Yae-Jean
Cho Eun-Young
Kim Hee-Soo
Guitton Fabrice
Ortiz Esteban
Abstract
Recommended infant vaccination in Korea includes DTaP-IPV and Hib vaccines administered as separate injections. In this randomized, open, controlled study we assessed the non-inferiority of immunogenicity of DTaP-IPV//Hib pentavalent combination vaccine (Pentaxim¢â) compared with licensed DTaP-IPV and Hib (PRP~T) vaccines. We enrolled 418 healthy Korean infants to receive either separate DTaP-IPV and Hib vaccines (n = 206) or the pentavalent DTaP-IPV//Hib (n = 208) vaccine at 2, 4, 6 months of age. Antibodies to all components were measured before the first vaccination and one month after the third, and safety was assessed after each vaccination including recording of reactions by parents. We confirmed the non-inferiority of DTaP-IPV//Hib compared with DTaP-IPV and Hib vaccines; 100% of both groups achieved seroprotection against D, T, IPV and PRP~T, and 97.5%?99.0% demonstrated seroresponses to pertussis antigens. Antibody levels were similar in both groups, except for those to the Hib component, PRP~T. In separate and combined groups geometric mean concentrations of anti-PRP~T antibodies were 23.9 and 11.0 ¥ìg/mL, respectively, but 98.3% and 97.4% had titers ¡Ã 1 ¥ìg/mL, indicative of long-term protection. All vaccines were well tolerated, with no vaccine-related serious adverse event. Both groups had similar safety profiles, but the combined vaccine group had fewer injection site reactions. The immunological non-inferiority and similar safety profile of DTaP-IPV//Hib vaccine to separate DTaP-IPV and Hib vaccines, with the advantage of fewer injections and injection site reactions, supports the licensure and incorporation of DTaP-IPV//Hib into the Korean national vaccination schedule (Clinical trial registry, NCT01214889).
KEYWORD
Immunogenicity, Safety, DTaP-IPV Vaccine, Hib Vaccine, Infants, Clinical Trial
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