4.7 Article

Safety and immunogenicity of co-administration of meningococcal type A and measles-rubella vaccines with typhoid conjugate vaccine in children aged 15-23 months in Burkina Faso

期刊

INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES
卷 102, 期 -, 页码 517-523

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ELSEVIER SCI LTD
DOI: 10.1016/j.ijid.2020.10.103

关键词

Typhoid conjugate vaccine; Meningococcal vaccines; Measles-rubella vaccine; Co-administration; Sub-Saharan Africa; Burkina Faso

资金

  1. Bill & Melinda Gates Foundation

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This study in Burkina Faso tested the co-administration of a single-dose typhoid conjugate vaccine with routine meningococcal conjugate vaccine and measles-rubella vaccine. The results showed that TCV can be safely co-administered with MCV-A at 15 months without interference, providing data to support large-scale uptake in sub-Saharan Africa.
Objectives: The World Health Organization pre-qualified single-dose typhoid conjugate vaccine (TCV) and requested data on co-administration with routine vaccines. The co-administration of Typbar TCV (Bharat Biotech International) with routine group A meningococcal conjugate vaccine (MCV-A) and measles- rubella (MR) vaccine was tested. Methods: This was a double-blind, randomized controlled trial performed in Ouagadougou, Burkina Faso. Children were recruited at the 15-month vaccination visit and were assigned randomly (1:1:1) to three groups. Group 1 children received TCV plus control vaccine (inactivated polio vaccine) and MCV-A 28 days later; group 2 children received TCV and MCV-A; group 3 children received MCV-A and control vaccine. Routine MR vaccine was administered to all participants. Safety was assessed at 0, 3, and 7 days after immunization, and unsolicited adverse events and serious adverse events were assessed for 28 days and 6 months after immunization, respectively. Results: A total of 150 children were recruited and vaccinated. Solicited symptoms were infrequent and similar for TCV and control recipients, as were adverse events (group 1, 61.2%; group 2, 64.0%; group 3, 68.6%) and serious adverse events (group 1, 2.0%; group 2, 8.0%; group 3, 5.9%). TCV generated robust immunity without interference with MCV-A vaccine. Conclusions: TCV can be safely co-administered at 15 months with MCV-A without interference. This novel study on the co-administration of TCV with MCV-A provides data to support large-scale uptake in sub-Saharan Africa. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.

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