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Immune Responses to an Oral Cholera Vaccine in Internally Displaced Persons in South Sudan

Despite recent large-scale cholera outbreaks, little is known about the immunogenicity of oral cholera vaccines (OCV) in African populations, particularly among those at highest cholera risk. During a 2015 preemptive OCV campaign among internally displaced persons in South Sudan, a year after a larg...

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Detalles Bibliográficos
Autores principales: Iyer, Anita S., Bouhenia, Malika, Rumunu, John, Abubakar, Abdinasir, Gruninger, Randon J., Pita, Jane, Lino, Richard Lako, Deng, Lul L., Wamala, Joseph F., Ryan, Edward T., Martin, Stephen, Legros, Dominique, Lessler, Justin, Sack, David A., Luquero, Francisco J., Leung, Daniel T., Azman, Andrew S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075787/
https://www.ncbi.nlm.nih.gov/pubmed/27775046
http://dx.doi.org/10.1038/srep35742
Descripción
Sumario:Despite recent large-scale cholera outbreaks, little is known about the immunogenicity of oral cholera vaccines (OCV) in African populations, particularly among those at highest cholera risk. During a 2015 preemptive OCV campaign among internally displaced persons in South Sudan, a year after a large cholera outbreak, we enrolled 37 young children (1–5 years old), 67 older children (6–17 years old) and 101 adults (≥18 years old), who received two doses of OCV (Shanchol) spaced approximately 3 weeks apart. Cholera-specific antibody responses were determined at days 0, 21 and 35 post-immunization. High baseline vibriocidal titers (>80) were observed in 21% of the participants, suggesting recent cholera exposure or vaccination. Among those with titers ≤80, 90% young children, 73% older children and 72% adults seroconverted (≥4 fold titer rise) after the 1(st) OCV dose; with no additional seroconversion after the 2(nd) dose. Post-vaccination immunological endpoints did not differ across age groups. Our results indicate Shanchol was immunogenic in this vulnerable population and that a single dose alone may be sufficient to achieve similar short-term immunological responses to the currently licensed two-dose regimen. While we found no evidence of differential response by age, further immunologic and epidemiologic studies are needed.