Microneedle patch delivery of influenza vaccine during pregnancy enhances maternal immune responses promoting survival and long-lasting passive immunity to offspring
Abstract Influenza virus causes life-threatening infections in pregnant women and their newborns. Immunization during pregnancy is the most effective means of preventing maternal and infant mortality/morbidity; however, influenza vaccination rates of pregnant women remain under 50%. Furthermore, the...
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Nature Portfolio
2017
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oai:doaj.org-article:bee56125b1cf4f40b60481bcbec9c6ab2021-12-02T16:07:59ZMicroneedle patch delivery of influenza vaccine during pregnancy enhances maternal immune responses promoting survival and long-lasting passive immunity to offspring10.1038/s41598-017-05940-72045-2322https://doaj.org/article/bee56125b1cf4f40b60481bcbec9c6ab2017-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-05940-7https://doaj.org/toc/2045-2322Abstract Influenza virus causes life-threatening infections in pregnant women and their newborns. Immunization during pregnancy is the most effective means of preventing maternal and infant mortality/morbidity; however, influenza vaccination rates of pregnant women remain under 50%. Furthermore, the availability of vaccines in low-resource populations is limited. Skin immunization with microneedle patches (MN) is a novel and safe vaccination platform featuring thermostable vaccine formulations. Cold-chain independence and the potential for self-administration can expand influenza vaccination coverage in developing countries. In this study of pregnant BALB/c mice immunized with subunit H1N1 influenza vaccine, we demonstrate the advantage of skin vaccination over intramuscular delivery of a two-fold higher vaccine dose. MN vaccine induced superior humoral immune responses and conferred protective immunity against a lethal challenge dose of homologous influenza virus. Importantly, MN vaccination of mice at mid-gestation resulted in enhanced and long-lasting passive immunity of the offspring, measured by neutralizing antibody titers and survival rates after virus challenge. We conclude that skin vaccination using MN is a superior immunization approach with the potential to overcome immune tolerance observed in pregnancy, and lower vaccination costs through antigen dose-sparing, which is especially relevant in underserved countries.E. Stein EsserJoanna A. Pulit-PenalozaHaripriya KalluriDevin McAllisterElena V. VassilievaElizabeth Q. LittauerNadia LelutiuMark R. PrausnitzRichard W. CompansIoanna SkountzouNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-11 (2017) |
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Medicine R Science Q E. Stein Esser Joanna A. Pulit-Penaloza Haripriya Kalluri Devin McAllister Elena V. Vassilieva Elizabeth Q. Littauer Nadia Lelutiu Mark R. Prausnitz Richard W. Compans Ioanna Skountzou Microneedle patch delivery of influenza vaccine during pregnancy enhances maternal immune responses promoting survival and long-lasting passive immunity to offspring |
description |
Abstract Influenza virus causes life-threatening infections in pregnant women and their newborns. Immunization during pregnancy is the most effective means of preventing maternal and infant mortality/morbidity; however, influenza vaccination rates of pregnant women remain under 50%. Furthermore, the availability of vaccines in low-resource populations is limited. Skin immunization with microneedle patches (MN) is a novel and safe vaccination platform featuring thermostable vaccine formulations. Cold-chain independence and the potential for self-administration can expand influenza vaccination coverage in developing countries. In this study of pregnant BALB/c mice immunized with subunit H1N1 influenza vaccine, we demonstrate the advantage of skin vaccination over intramuscular delivery of a two-fold higher vaccine dose. MN vaccine induced superior humoral immune responses and conferred protective immunity against a lethal challenge dose of homologous influenza virus. Importantly, MN vaccination of mice at mid-gestation resulted in enhanced and long-lasting passive immunity of the offspring, measured by neutralizing antibody titers and survival rates after virus challenge. We conclude that skin vaccination using MN is a superior immunization approach with the potential to overcome immune tolerance observed in pregnancy, and lower vaccination costs through antigen dose-sparing, which is especially relevant in underserved countries. |
format |
article |
author |
E. Stein Esser Joanna A. Pulit-Penaloza Haripriya Kalluri Devin McAllister Elena V. Vassilieva Elizabeth Q. Littauer Nadia Lelutiu Mark R. Prausnitz Richard W. Compans Ioanna Skountzou |
author_facet |
E. Stein Esser Joanna A. Pulit-Penaloza Haripriya Kalluri Devin McAllister Elena V. Vassilieva Elizabeth Q. Littauer Nadia Lelutiu Mark R. Prausnitz Richard W. Compans Ioanna Skountzou |
author_sort |
E. Stein Esser |
title |
Microneedle patch delivery of influenza vaccine during pregnancy enhances maternal immune responses promoting survival and long-lasting passive immunity to offspring |
title_short |
Microneedle patch delivery of influenza vaccine during pregnancy enhances maternal immune responses promoting survival and long-lasting passive immunity to offspring |
title_full |
Microneedle patch delivery of influenza vaccine during pregnancy enhances maternal immune responses promoting survival and long-lasting passive immunity to offspring |
title_fullStr |
Microneedle patch delivery of influenza vaccine during pregnancy enhances maternal immune responses promoting survival and long-lasting passive immunity to offspring |
title_full_unstemmed |
Microneedle patch delivery of influenza vaccine during pregnancy enhances maternal immune responses promoting survival and long-lasting passive immunity to offspring |
title_sort |
microneedle patch delivery of influenza vaccine during pregnancy enhances maternal immune responses promoting survival and long-lasting passive immunity to offspring |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/bee56125b1cf4f40b60481bcbec9c6ab |
work_keys_str_mv |
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