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dc.contributor.author
Libster, Romina Paula  
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McNeal, Monica  
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Walter, Emmanuel B.  
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Shane, Andi L.  
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Winokur, Patricia  
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Cress, Gretchen  
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Berry, Andrea A.  
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Kotloff, Karen L.  
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Sarpong, Kwabena  
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Turley, Christine B.  
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Harrison, Christopher J.  
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Pahud, Barbara A.  
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Marbin, Jyothi  
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Dunn, John  
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El-Khorazaty, Jill  
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Barret, Jill  
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Edwards, Kathryn M  
dc.date.available
2019-11-21T21:16:00Z  
dc.date.issued
2016-02  
dc.identifier.citation
Libster, Romina Paula; McNeal, Monica; Walter, Emmanuel B.; Shane, Andi L.; Winokur, Patricia; et al.; Safety and immunogenicity of sequential rotavirus vaccine schedules; American Academy of Pediatrics; Pediatrics; 137; 2; 2-2016; 1-10  
dc.identifier.issn
0031-4005  
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http://hdl.handle.net/11336/89492  
dc.description.abstract
BACKGROUND AND OBJECTIVES: Although both licensed rotavirus vaccines are safe and effective, it is often not possible to complete the schedule by using the same vaccine formulation. The goal of this study was to investigate the noninferiority of the immune responses to the 2 licensed rotavirus vaccines when administered as a mixed schedule compared with administering a single vaccine formulation alone. METHODS: Randomized, multicenter, open-label study. Healthy infants (6-14 weeks of age) were randomized to receive rotavirus vaccines in 1 of 5 different schedules (2 using a single vaccine for all doses, and 3 using mixed schedules). The group receiving only the monovalent rotavirus vaccine received 2 doses of vaccine and the other 4 groups received 3 doses of vaccine. Serum for immunogenicity testing was obtained 1 month after the last vaccine dose and the proportion of seropositive children (rotavirus immunoglobulin A >20 U/mL) were compared in all the vaccine groups. RESULTS: Between March 2011 and September 2013, 1393 children were enrolled and randomized. Immune responses to all the sequential mixed vaccine schedules were shown to be noninferior when compared with the 2 single vaccine reference groups. The proportion of children seropositive to at least 1 vaccine antigen at 1 month after vaccination ranged from 77% to 96%, and was not significantly different among all the study groups. All schedules were well tolerated. CONCLUSIONS: Mixed schedules are safe and induced comparable immune responses when compared with the licensed rotavirus vaccines given alone.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
American Academy of Pediatrics  
dc.rights
info:eu-repo/semantics/openAccess  
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https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
rotavirus  
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rotavirus vaccine  
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schedule  
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Enfermedades Infecciosas  
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Ciencias de la Salud  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Safety and immunogenicity of sequential rotavirus vaccine schedules  
dc.type
info:eu-repo/semantics/article  
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info:ar-repo/semantics/artículo  
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info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-11-15T15:27:21Z  
dc.journal.volume
137  
dc.journal.number
2  
dc.journal.pagination
1-10  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Elk Grove Village  
dc.description.fil
Fil: Libster, Romina Paula. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Fundación para la Investigación en Infectología Infantil; Argentina. Vanderbilt University; Estados Unidos  
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Fil: McNeal, Monica. Cincinnati Children's Hospital Medical Center; Estados Unidos  
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Fil: Walter, Emmanuel B.. Duke University School Of Medicine; Estados Unidos  
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Fil: Shane, Andi L.. University of Emory; Estados Unidos  
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Fil: Winokur, Patricia. University of Iowa; Estados Unidos  
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Fil: Cress, Gretchen. University of Iowa; Estados Unidos  
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Fil: Berry, Andrea A.. University of Maryland; Estados Unidos  
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Fil: Kotloff, Karen L.. University of Maryland; Estados Unidos  
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Fil: Sarpong, Kwabena. University of Texas Medical Branch; Estados Unidos  
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Fil: Turley, Christine B.. University of Texas Medical Branch; Estados Unidos  
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Fil: Harrison, Christopher J.. Children's Mercy Hospital; Estados Unidos  
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Fil: Pahud, Barbara A.. Children's Mercy Hospital; Estados Unidos  
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Fil: Marbin, Jyothi. Benioff Children's Hospital Oakland; Estados Unidos  
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Fil: Dunn, John. Group Health Cooperative; Estados Unidos  
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Fil: El-Khorazaty, Jill. Emmes Corporation; Estados Unidos  
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Fil: Barret, Jill. Emmes Corporation; Estados Unidos  
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Fil: Edwards, Kathryn M. Vanderbilt University; Estados Unidos  
dc.journal.title
Pediatrics  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://pediatrics.aappublications.org/content/137/2/e20152603  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1542/peds.2015-2603