Abstract

This author reply letter discusses three topics that highlight the successful results and major implications of the study for the development of a rotavirus vaccine and its clinical evaluation in developing countries. It touches on: the concept of the natural molecular evolution of rotavirus strains the potential heterotypic cross-protection offered by the monovalent G1P[8] rotavirus vaccine against strains with neither G1 nor P[8] specificity and the concept of potential interference in vaccine efficacy from antibodies in breast milk.

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