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Correlates of Immune Protection Against Human Rotaviruses: Natural Infection and Vaccination Publisher Pubmed



Latifi T1 ; Kachooei A2, 3 ; Jalilvand S4 ; Zafarian S5 ; Roohvand F2 ; Shoja Z2, 6
Authors
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Authors Affiliations
  1. 1. Department of Microbiology and Immunology, Carver College of Medicine, University of Iowa, Iowa City, United States
  2. 2. Department of Virology, Pasteur Institute of Iran, Tehran, Iran
  3. 3. Department of Virology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Microbial Biotechnology, College of Science, University of Tehran, Tehran, Iran
  6. 6. Research Center for Emerging and Reemerging Infectious Diseases, Pasteur Institute of Iran, Tehran, Iran

Source: Archives of Virology Published:2024


Abstract

Species A rotaviruses are the leading viral cause of acute gastroenteritis in children under 5 years of age worldwide. Despite progress in the characterization of the pathogenesis and immunology of rotavirus-induced gastroenteritis, correlates of protection (CoPs) in the course of either natural infection or vaccine-induced immunity are not fully understood. There are numerous factors such as serological responses (IgA and IgG), the presence of maternal antibodies (Abs) in breast milk, changes in the intestinal microbiome, and rotavirus structural and non-structural proteins that contribute to the outcome of the CoP. Indeed, while an intestinal IgA response and its surrogate, the serum IgA level, are suggested as the principal CoPs for oral rotavirus vaccines, the IgG level is more likely to be a CoP for parenteral non-replicating rotavirus vaccines. Integrating clinical and immunological data will be instrumental in improving rotavirus vaccine efficacy, especially in low- and middle-income countries, where vaccine efficacy is significantly lower than in high-income countries. Further knowledge on CoPs against rotavirus disease will be helpful for next-generation vaccine development. Herein, available data and literature on interacting components and proposed CoPs against human rotavirus disease are reviewed, and limitations and gaps in our knowledge in this area are discussed. © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2024.
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