Immunogenicity and Safety of a Hexavalent DTwP-IPV-HB-PRP~T Vaccine Versus Separate DTwP-HB-PRP~T, bOPV, and IPV Vaccines Administered at 2, 4, 6 Months of Age Concomitantly With Rotavirus and Pneumococcal Conjugate Vaccines in Healthy Infants in Thailand

dc.contributor.authorSanchez L.
dc.contributor.authorRungmaitree S.
dc.contributor.authorKosalaraksa P.
dc.contributor.authorJantarabenjakul W.
dc.contributor.authorLeclercq J.
dc.contributor.authorYaiprayoon Y.
dc.contributor.authorMidde V.J.
dc.contributor.authorVarghese K.
dc.contributor.authorMangarule S.
dc.contributor.authorNoriega F.
dc.contributor.otherMahidol University
dc.date.accessioned2023-07-28T18:01:30Z
dc.date.available2023-07-28T18:01:30Z
dc.date.issued2023-08-01
dc.description.abstractBACKGROUND: This study investigated the immunogenicity and safety of a fully liquid, hexavalent, diphtheria (D)-tetanus (T)-whole-cell pertussis (wP)-inactivated poliovirus (IPV)-hepatitis B (HB)- Haemophilus influenzae b (PRP-T) vaccine compared to licensed DTwP-HB-PRP~T, IPV, and bivalent oral poliovirus (bOPV) vaccines following co-administration with other pediatric vaccines [pneumococcal conjugate vaccine (PCV13) and rotavirus vaccine]. METHODS: Phase III, randomized, open-label study in Thailand. Healthy infants received DTwP-IPV-HB-PRP~T at 2, 4 and 6 months of age (N = 228), or DTwP-HB-PRP~T and bOPV (2, 4 and 6 months of age) and IPV (4 months of age) (N = 231). All participants received PCV13 (2, 4 and 6 months of age) and rotavirus vaccine (2 and 4 months of age). Immunogenicity for all antigens was assessed using validated assays, and noninferiority post-third dose was evaluated for anti-D, anti-T, anti-pertussis [anti-pertussis toxin (anti-PT) and anti-fimbriae 2/3 (anti-FIM)], anti-polio 1, 2, 3, anti-HB, and anti-PRP~T. Safety was assessed using parental reports. RESULTS: Noninferiority was demonstrated for each antigen, and overall noninferiority of DTwP-IPV-HB-PRP~T versus DTwP-HB-PRP~T+bOPV+IPV was concluded. Similarity in each group was observed for the GMC ratio for antirotavirus antibodies (20.9 and 17.3, respectively) and anti-PCV13 antibodies (range: 8.46-32.6 and 7.53-33.1, respectively). Two serious adverse events were related to DTwP-IPV-HB-PRP~T (febrile convulsion and acute febrile illness) and 1 was related to DTwP-HB-PRP~T+bOPV+IPV (febrile seizure), but overall there were no safety concerns with similar rates of participants experiencing solicited (99.1% and 98.3%) and unsolicited (19.3% and 19.5%) adverse events in each group. CONCLUSIONS: This study confirmed the suitability of DTwP-IPV-HB-PRP~T primary series vaccination in combination with rotavirus and PCV13 vaccines.
dc.identifier.citationThe Pediatric infectious disease journal Vol.42 No.8 (2023) , 711-718
dc.identifier.doi10.1097/INF.0000000000003975
dc.identifier.eissn15320987
dc.identifier.pmid37257121
dc.identifier.scopus2-s2.0-85165224523
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/88114
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleImmunogenicity and Safety of a Hexavalent DTwP-IPV-HB-PRP~T Vaccine Versus Separate DTwP-HB-PRP~T, bOPV, and IPV Vaccines Administered at 2, 4, 6 Months of Age Concomitantly With Rotavirus and Pneumococcal Conjugate Vaccines in Healthy Infants in Thailand
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85165224523&origin=inward
oaire.citation.endPage718
oaire.citation.issue8
oaire.citation.startPage711
oaire.citation.titleThe Pediatric infectious disease journal
oaire.citation.volume42
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationFaculty of Medicine, Khon Kaen University
oairecerif.author.affiliationKing Chulalongkorn Memorial Hospital
oairecerif.author.affiliationSanofi S.A.
oairecerif.author.affiliationFaculty of Medicine, Chulalongkorn University
oairecerif.author.affiliationSanofi
oairecerif.author.affiliationFrom the Sanofi
oairecerif.author.affiliationSanofi

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