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1.
J Pediatric Infect Dis Soc ; 12(9): 513-518, 2023 Sep 27.
Artigo em Inglês | MEDLINE | ID: mdl-37589596

RESUMO

We assessed anti-Vi IgG/IgA responses to typhoid conjugate vaccine (TCV) in children enrolled in a double-blind randomized controlled, phase 2 trial in Burkina Faso. Anti-Vi IgG seroconversion and anti-Vi IgA titers were higher in TCV than control recipients at 30-35 months post-vaccination. TCV induces durable immunity in Burkinabe children vaccinated at 15 months.


Assuntos
Febre Tifoide , Vacinas Tíficas-Paratíficas , Humanos , Criança , Lactente , Febre Tifoide/prevenção & controle , Vacinas Conjugadas , Burkina Faso , Formação de Anticorpos , Imunoglobulina A , Imunoglobulina G , Anticorpos Antibacterianos
2.
Int J Infect Dis ; 108: 465-472, 2021 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-34082090

RESUMO

OBJECTIVES: In 2017, the World Health Organisation (WHO) pre-qualified a single-dose typhoid conjugate vaccine (TCV) and identified TCV co-administration studies as a research priority. Accordingly, we tested co-administration of Typbar TCV® (Bharat Biotech International) with measles-rubella (MR) and yellow fever (YF) vaccines. METHODS: We conducted a randomized, double-blind, and controlled, phase 2 trial in Ouagadougou, Burkina Faso. Healthy children aged 9-11 months were randomized 1:1 to receive TCV (Group 1) or control vaccine (inactivated polio vaccine (IPV), Group 2). Vaccines were administered intramuscularly with routine MR and YF vaccines. Safety was assessed by (1) local and systemic reactions on days 0, 3, and 7; (2) unsolicited adverse events within 28 days; and (3) serious adverse events (SAEs) within six months after immunization. RESULTS: We enrolled, randomized, and vaccinated 100 eligible children (49 Group 1 and 51 Group 2). Safety outcomes occurred with similar frequency in both groups: local/solicited reactions (Group 1: 1/49, Group 2: 3/50), systemic/solicited reactions (Group 1: 4/49, Group 2: 9/50), unsolicited adverse events (Group 1: 26/49, Group 2: 33/51), and SAEs (Group 1: 2/49, Group 2: 3/51). TCV conferred robust immunogenicity without interference with MR or YF vaccines. CONCLUSION: TCV can be safely co-administered with MR and YF vaccines to children at the 9-month vaccination visit.


Assuntos
Polissacarídeos Bacterianos/efeitos adversos , Vacinas Tíficas-Paratíficas/efeitos adversos , Burkina Faso , Método Duplo-Cego , Feminino , Humanos , Lactente , Masculino , Vacina contra Sarampo/administração & dosagem , Polissacarídeos Bacterianos/administração & dosagem , Polissacarídeos Bacterianos/imunologia , Vacina contra Rubéola/administração & dosagem , Vacinas Tíficas-Paratíficas/administração & dosagem , Vacinas Tíficas-Paratíficas/imunologia , Vacinas Conjugadas/efeitos adversos , Vacinas Conjugadas/imunologia , Vacina contra Febre Amarela/administração & dosagem
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