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dc.contributor.authorBlanco, Jorge C G
dc.contributor.authorCullen, Lori McGinnes
dc.contributor.authorKamali, Arash
dc.contributor.authorSylla, Fatoumata Y D
dc.contributor.authorChinmoun, Zenab
dc.contributor.authorBoukhvalova, Marina S
dc.contributor.authorMorrison, Trudy G.
dc.date.accessioned2024-04-17T15:44:10Z
dc.date.available2024-04-17T15:44:10Z
dc.date.issued2022-12-12
dc.identifier.citationBlanco JCG, Cullen LM, Kamali A, Sylla FYD, Chinmoun Z, Boukhvalova MS, Morrison TG. Correlative outcomes of maternal immunization against RSV in cotton rats. Hum Vaccin Immunother. 2022 Dec 30;18(7):2148499. doi: 10.1080/21645515.2022.2148499. Epub 2022 Dec 12. PMID: 36503354; PMCID: PMC9766472.en_US
dc.identifier.eissn2164-554X
dc.identifier.doi10.1080/21645515.2022.2148499en_US
dc.identifier.pmid36503354
dc.identifier.urihttp://hdl.handle.net/20.500.14038/53288
dc.description.abstractMaternal anti-respiratory syncytial virus (RSV) antibodies protect neonates from RSV disease throughout first weeks of life. Previous studies of maternal immunization in cotton rats showed that a single immunization during pregnancy of RSV-primed dams with virus-like particles (VLPs) assembled with pre-fusion F protein and the wild type G protein boosted their RSV serum antibody concentration and protected pups early in life against RSV challenge. We extended these findings by evaluating responses to RSV infection in litters from two consecutive pregnancies of immunized dams. Using an RSV-primed population of VLP-vaccinated and unvaccinated dams, we defined correlations between dams' and litters' RSV neutralizing antibodies (NA); between litters' NA and protection; and between litter's NA and their lung expression of selected cytokines, of a first or of a second pregnancy. Lung pathology was also evaluated. We found positive correlation between the NA titers in the dams at delivery and the NA in their first and second litters and negative correlations between the litters' NA and protection from RSV challenge. Vaccination of dams modulated the mRNA expression for IFNγ and IL-6 and lung pathology in the first and in the second litter at different times after birth, even in the absence of detectable NA. Maternal RSV vaccination enhanced the levels of antibodies transferred to offspring and their protection from challenge. Importantly, maternal vaccination also impacted the immunological and inflammatory response of the offspring's lungs well into maturity, and after the antiviral effect of maternally transferred NA waned or was no longer detectable.en_US
dc.language.isoenen_US
dc.relation.ispartofHuman Vaccines & Immunotherapeuticsen_US
dc.relation.urlhttps://doi.org/10.1080/21645515.2022.2148499en_US
dc.rights© 2022 The Author(s). Published with license by Taylor & Francis Group, LLC. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any wayen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectMaternal Vaccinationen_US
dc.subjectRSV Vaccinationen_US
dc.subjectcotton raten_US
dc.subjectpregnancyen_US
dc.titleCorrelative outcomes of maternal immunization against RSV in cotton ratsen_US
dc.typeJournal Articleen_US
dc.source.journaltitleHuman vaccines & immunotherapeutics
dc.source.volume18
dc.source.issue7
dc.source.beginpage2148499
dc.source.endpage
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.identifier.journalHuman vaccines & immunotherapeutics
refterms.dateFOA2024-04-17T15:44:12Z
dc.contributor.departmentMicrobiology and Physiological Systemsen_US


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© 2022 The Author(s). Published with license by Taylor & Francis Group, LLC.
This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/),
which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way
Except where otherwise noted, this item's license is described as © 2022 The Author(s). Published with license by Taylor & Francis Group, LLC. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way