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Impact of maternal antibodies and microbiota development on the immunogenicity of oral rotavirus vaccine in African, Indian, and European infants

Identifying risk factors for impaired oral rotavirus vaccine (ORV) efficacy in low-income countries may lead to improvements in vaccine design and delivery. In this prospective cohort study, we measure maternal rotavirus antibodies, environmental enteric dysfunction (EED), and bacterial gut microbio...

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Autores principales: Parker, Edward P. K., Bronowski, Christina, Sindhu, Kulandaipalayam Natarajan C., Babji, Sudhir, Benny, Blossom, Carmona-Vicente, Noelia, Chasweka, Nedson, Chinyama, End, Cunliffe, Nigel A., Dube, Queen, Giri, Sidhartha, Grassly, Nicholas C., Gunasekaran, Annai, Howarth, Deborah, Immanuel, Sushil, Jere, Khuzwayo C., Kampmann, Beate, Lowe, Jenna, Mandolo, Jonathan, Praharaj, Ira, Rani, Bakthavatsalam Sandya, Silas, Sophia, Srinivasan, Vivek Kumar, Turner, Mark, Venugopal, Srinivasan, Verghese, Valsan Philip, Darby, Alistair C., Kang, Gagandeep, Iturriza-Gómara, Miren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674366/
https://www.ncbi.nlm.nih.gov/pubmed/34911947
http://dx.doi.org/10.1038/s41467-021-27074-1
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author Parker, Edward P. K.
Bronowski, Christina
Sindhu, Kulandaipalayam Natarajan C.
Babji, Sudhir
Benny, Blossom
Carmona-Vicente, Noelia
Chasweka, Nedson
Chinyama, End
Cunliffe, Nigel A.
Dube, Queen
Giri, Sidhartha
Grassly, Nicholas C.
Gunasekaran, Annai
Howarth, Deborah
Immanuel, Sushil
Jere, Khuzwayo C.
Kampmann, Beate
Lowe, Jenna
Mandolo, Jonathan
Praharaj, Ira
Rani, Bakthavatsalam Sandya
Silas, Sophia
Srinivasan, Vivek Kumar
Turner, Mark
Venugopal, Srinivasan
Verghese, Valsan Philip
Darby, Alistair C.
Kang, Gagandeep
Iturriza-Gómara, Miren
author_facet Parker, Edward P. K.
Bronowski, Christina
Sindhu, Kulandaipalayam Natarajan C.
Babji, Sudhir
Benny, Blossom
Carmona-Vicente, Noelia
Chasweka, Nedson
Chinyama, End
Cunliffe, Nigel A.
Dube, Queen
Giri, Sidhartha
Grassly, Nicholas C.
Gunasekaran, Annai
Howarth, Deborah
Immanuel, Sushil
Jere, Khuzwayo C.
Kampmann, Beate
Lowe, Jenna
Mandolo, Jonathan
Praharaj, Ira
Rani, Bakthavatsalam Sandya
Silas, Sophia
Srinivasan, Vivek Kumar
Turner, Mark
Venugopal, Srinivasan
Verghese, Valsan Philip
Darby, Alistair C.
Kang, Gagandeep
Iturriza-Gómara, Miren
author_sort Parker, Edward P. K.
collection PubMed
description Identifying risk factors for impaired oral rotavirus vaccine (ORV) efficacy in low-income countries may lead to improvements in vaccine design and delivery. In this prospective cohort study, we measure maternal rotavirus antibodies, environmental enteric dysfunction (EED), and bacterial gut microbiota development among infants receiving two doses of Rotarix in India (n = 307), Malawi (n = 119), and the UK (n = 60), using standardised methods across cohorts. We observe ORV shedding and seroconversion rates to be significantly lower in Malawi and India than the UK. Maternal rotavirus-specific antibodies in serum and breastmilk are negatively correlated with ORV response in India and Malawi, mediated partly by a reduction in ORV shedding. In the UK, ORV shedding is not inhibited despite comparable maternal antibody levels to the other cohorts. In both India and Malawi, increased microbiota diversity is negatively correlated with ORV immunogenicity, suggesting that high early-life microbial exposure may contribute to impaired vaccine efficacy.
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spelling pubmed-86743662022-01-04 Impact of maternal antibodies and microbiota development on the immunogenicity of oral rotavirus vaccine in African, Indian, and European infants Parker, Edward P. K. Bronowski, Christina Sindhu, Kulandaipalayam Natarajan C. Babji, Sudhir Benny, Blossom Carmona-Vicente, Noelia Chasweka, Nedson Chinyama, End Cunliffe, Nigel A. Dube, Queen Giri, Sidhartha Grassly, Nicholas C. Gunasekaran, Annai Howarth, Deborah Immanuel, Sushil Jere, Khuzwayo C. Kampmann, Beate Lowe, Jenna Mandolo, Jonathan Praharaj, Ira Rani, Bakthavatsalam Sandya Silas, Sophia Srinivasan, Vivek Kumar Turner, Mark Venugopal, Srinivasan Verghese, Valsan Philip Darby, Alistair C. Kang, Gagandeep Iturriza-Gómara, Miren Nat Commun Article Identifying risk factors for impaired oral rotavirus vaccine (ORV) efficacy in low-income countries may lead to improvements in vaccine design and delivery. In this prospective cohort study, we measure maternal rotavirus antibodies, environmental enteric dysfunction (EED), and bacterial gut microbiota development among infants receiving two doses of Rotarix in India (n = 307), Malawi (n = 119), and the UK (n = 60), using standardised methods across cohorts. We observe ORV shedding and seroconversion rates to be significantly lower in Malawi and India than the UK. Maternal rotavirus-specific antibodies in serum and breastmilk are negatively correlated with ORV response in India and Malawi, mediated partly by a reduction in ORV shedding. In the UK, ORV shedding is not inhibited despite comparable maternal antibody levels to the other cohorts. In both India and Malawi, increased microbiota diversity is negatively correlated with ORV immunogenicity, suggesting that high early-life microbial exposure may contribute to impaired vaccine efficacy. Nature Publishing Group UK 2021-12-15 /pmc/articles/PMC8674366/ /pubmed/34911947 http://dx.doi.org/10.1038/s41467-021-27074-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Parker, Edward P. K.
Bronowski, Christina
Sindhu, Kulandaipalayam Natarajan C.
Babji, Sudhir
Benny, Blossom
Carmona-Vicente, Noelia
Chasweka, Nedson
Chinyama, End
Cunliffe, Nigel A.
Dube, Queen
Giri, Sidhartha
Grassly, Nicholas C.
Gunasekaran, Annai
Howarth, Deborah
Immanuel, Sushil
Jere, Khuzwayo C.
Kampmann, Beate
Lowe, Jenna
Mandolo, Jonathan
Praharaj, Ira
Rani, Bakthavatsalam Sandya
Silas, Sophia
Srinivasan, Vivek Kumar
Turner, Mark
Venugopal, Srinivasan
Verghese, Valsan Philip
Darby, Alistair C.
Kang, Gagandeep
Iturriza-Gómara, Miren
Impact of maternal antibodies and microbiota development on the immunogenicity of oral rotavirus vaccine in African, Indian, and European infants
title Impact of maternal antibodies and microbiota development on the immunogenicity of oral rotavirus vaccine in African, Indian, and European infants
title_full Impact of maternal antibodies and microbiota development on the immunogenicity of oral rotavirus vaccine in African, Indian, and European infants
title_fullStr Impact of maternal antibodies and microbiota development on the immunogenicity of oral rotavirus vaccine in African, Indian, and European infants
title_full_unstemmed Impact of maternal antibodies and microbiota development on the immunogenicity of oral rotavirus vaccine in African, Indian, and European infants
title_short Impact of maternal antibodies and microbiota development on the immunogenicity of oral rotavirus vaccine in African, Indian, and European infants
title_sort impact of maternal antibodies and microbiota development on the immunogenicity of oral rotavirus vaccine in african, indian, and european infants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674366/
https://www.ncbi.nlm.nih.gov/pubmed/34911947
http://dx.doi.org/10.1038/s41467-021-27074-1
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