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Randomized clinical trial of DTaP5-HB-IPV-Hib vaccine administered concomitantly with meningococcal serogroup C conjugate vaccines during the primary infant series.

Oliver, JL; Sadorge, C; Boisnard, F; Snape, MD; Tomlinson, R; Mann, R; Rudd, P; Bhakthavalsala, S; Faust, SN; Heath, PT; et al. Oliver, JL; Sadorge, C; Boisnard, F; Snape, MD; Tomlinson, R; Mann, R; Rudd, P; Bhakthavalsala, S; Faust, SN; Heath, PT; Hughes, SM; Borrow, R; Thomas, S; Finn, A (2020) Randomized clinical trial of DTaP5-HB-IPV-Hib vaccine administered concomitantly with meningococcal serogroup C conjugate vaccines during the primary infant series. Vaccine, 38 (35). pp. 5718-5725. ISSN 1873-2518 https://doi.org/10.1016/j.vaccine.2020.06.015
SGUL Authors: Heath, Paul Trafford

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Abstract

BACKGROUND: Concomitant administration of vaccines simplifies delivery. DTaP5-HB-IPV-Hib is a fully liquid, combination vaccine against 6 diseases. This study evaluated the compatibility of DTaP5-HB-IPV-Hib with 2 different meningococcus group C conjugate (MCC) vaccines in infants. METHODS: In a phase 3, open-label study, 284 healthy infants from 11 UK centres received DTaP5-HB-IPV-Hib at age 2, 3, and 4 months; 13-valent pneumococcal conjugate vaccine (PCV13) at 2 and 4 months; a Haemophilus influenzae type b (Hib)-MCC vaccine and a measles/mumps/rubella vaccine at 12 months. Participants were randomised 1:1 to receive either an MCC-detoxified tetanus toxin vaccine (MCC-TT; n = 141) or an MCC-Corynebacterium diphtheriae CRM197 protein vaccine (MCC-CRM; n = 143) at 3 and 4 months. The primary outcome was seroprotection rate (SPR) to MCC (percent with rabbit complement serum bactericidal antibody titer ≥8). RESULTS: Per protocol analysis, MCC SPRs were 100 and 96.4 one month after the first dose, 100 and 99.1 after the second dose, and 100 and 97.3 after the third (booster) dose of MCC in the MCC-TT and MCC-CRM groups, respectively. One month after all 3 doses of DTaP5-HB-IPV-Hib, immunoglobulin G anti-polyribosylribitol phosphate SPRs (% ≥0.15 µg/mL) were 97.8 in the MCC-TT group and 100 in the MCC-CRM group; anti-hepatitis B antigen SPRs (% ≥10 mIU/mL) were 96.8 and 96.3 in the MCC-TT and MCC-CRM groups, respectively. All participants were seroprotected against diphtheria and tetanus (≥0.01 IU/mL) and poliovirus types 1, 2, and 3 (≥8 dilution), and seroresponse rates to all pertussis antigens were ≥90.4%. Two vaccine-related serious adverse events (transient severe abdominal pain and crying) occurred concomitantly in 1 participant in the MCC-CRM group. Adverse event rates were similar to other studies of DTaP5-HB-IPV-Hib, with pyrexia ≥38 °C in 10.9% of participants following any dose. CONCLUSIONS: DTaP5-HB-IPV-Hib can be effectively used in a 2-, 3-, and 4-month infant priming schedule when given with 2 doses of MCC.

Item Type: Article
Additional Information: © 2020. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
Keywords: Antigen, Children, Combination, Immunization, Meningococcus, Vaccine, Animals, Antibodies, Bacterial, Diphtheria-Tetanus-Pertussis Vaccine, Haemophilus Vaccines, Haemophilus influenzae type b, Humans, Infant, Meningococcal Vaccines, Poliovirus Vaccine, Inactivated, Rabbits, Serogroup, Vaccines, Combined, Vaccines, Conjugate, Animals, Rabbits, Humans, Haemophilus influenzae type b, Diphtheria-Tetanus-Pertussis Vaccine, Haemophilus Vaccines, Meningococcal Vaccines, Vaccines, Combined, Poliovirus Vaccine, Inactivated, Vaccines, Conjugate, Antibodies, Bacterial, Infant, Serogroup, Vaccine, Meningococcus, Combination, Children, Immunization, Antigen, Antigen, Children, Combination, Immunization, Meningococcus, Vaccine, 06 Biological Sciences, 07 Agricultural and Veterinary Sciences, 11 Medical and Health Sciences, Virology
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Vaccine
ISSN: 1873-2518
Language: eng
Dates:
DateEvent
31 July 2020Published
10 July 2020Published Online
5 June 2020Accepted
Publisher License: Creative Commons: Attribution-Noncommercial-No Derivative Works 4.0
PubMed ID: 32654902
Web of Science ID: WOS:000551631300024
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/113459
Publisher's version: https://doi.org/10.1016/j.vaccine.2020.06.015

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