Immunologic mechanisms of seasonal influenza vaccination administered by microneedle patch from a randomized phase I trial

Abstract In a phase 1 randomized, single-center clinical trial, inactivated influenza virus vaccine delivered through dissolvable microneedle patches (MNPs) was found to be safe and immunogenic. Here, we compare the humoral and cellular immunologic responses in a subset of participants receiving inf...

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Autores principales: Nadine G. Rouphael, Lilin Lai, Sonia Tandon, Michele Paine McCullough, Yunchuan Kong, Sarah Kabbani, Muktha S. Natrajan, Yongxian Xu, Yerun Zhu, Dongli Wang, Jesse O’Shea, Amy Sherman, Tianwei Yu, Sebastien Henry, Devin McAllister, Daniel Stadlbauer, Surender Khurana, Hana Golding, Florian Krammer, Mark J. Mulligan, Mark R. Prausnitz
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/5b49040c2002496f8128ac3623836663
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spelling oai:doaj.org-article:5b49040c2002496f8128ac36238366632021-12-02T16:09:39ZImmunologic mechanisms of seasonal influenza vaccination administered by microneedle patch from a randomized phase I trial10.1038/s41541-021-00353-02059-0105https://doaj.org/article/5b49040c2002496f8128ac36238366632021-07-01T00:00:00Zhttps://doi.org/10.1038/s41541-021-00353-0https://doaj.org/toc/2059-0105Abstract In a phase 1 randomized, single-center clinical trial, inactivated influenza virus vaccine delivered through dissolvable microneedle patches (MNPs) was found to be safe and immunogenic. Here, we compare the humoral and cellular immunologic responses in a subset of participants receiving influenza vaccination by MNP to the intramuscular (IM) route of administration. We collected serum, plasma, and peripheral blood mononuclear cells in 22 participants up to 180 days post-vaccination. Hemagglutination inhibition (HAI) titers and antibody avidity were similar after MNP and IM vaccination, even though MNP vaccination used a lower antigen dose. MNPs generated higher neuraminidase inhibition (NAI) titers for all three influenza virus vaccine strains tested and triggered a larger percentage of circulating T follicular helper cells (CD4 + CXCR5 + CXCR3 + ICOS + PD-1+) compared to the IM route. Our study indicates that inactivated influenza virus vaccination by MNP produces humoral and cellular immune response that are similar or greater than IM vaccination.Nadine G. RouphaelLilin LaiSonia TandonMichele Paine McCulloughYunchuan KongSarah KabbaniMuktha S. NatrajanYongxian XuYerun ZhuDongli WangJesse O’SheaAmy ShermanTianwei YuSebastien HenryDevin McAllisterDaniel StadlbauerSurender KhuranaHana GoldingFlorian KrammerMark J. MulliganMark R. PrausnitzNature PortfolioarticleImmunologic diseases. AllergyRC581-607Neoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENnpj Vaccines, Vol 6, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Immunologic diseases. Allergy
RC581-607
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle Immunologic diseases. Allergy
RC581-607
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Nadine G. Rouphael
Lilin Lai
Sonia Tandon
Michele Paine McCullough
Yunchuan Kong
Sarah Kabbani
Muktha S. Natrajan
Yongxian Xu
Yerun Zhu
Dongli Wang
Jesse O’Shea
Amy Sherman
Tianwei Yu
Sebastien Henry
Devin McAllister
Daniel Stadlbauer
Surender Khurana
Hana Golding
Florian Krammer
Mark J. Mulligan
Mark R. Prausnitz
Immunologic mechanisms of seasonal influenza vaccination administered by microneedle patch from a randomized phase I trial
description Abstract In a phase 1 randomized, single-center clinical trial, inactivated influenza virus vaccine delivered through dissolvable microneedle patches (MNPs) was found to be safe and immunogenic. Here, we compare the humoral and cellular immunologic responses in a subset of participants receiving influenza vaccination by MNP to the intramuscular (IM) route of administration. We collected serum, plasma, and peripheral blood mononuclear cells in 22 participants up to 180 days post-vaccination. Hemagglutination inhibition (HAI) titers and antibody avidity were similar after MNP and IM vaccination, even though MNP vaccination used a lower antigen dose. MNPs generated higher neuraminidase inhibition (NAI) titers for all three influenza virus vaccine strains tested and triggered a larger percentage of circulating T follicular helper cells (CD4 + CXCR5 + CXCR3 + ICOS + PD-1+) compared to the IM route. Our study indicates that inactivated influenza virus vaccination by MNP produces humoral and cellular immune response that are similar or greater than IM vaccination.
format article
author Nadine G. Rouphael
Lilin Lai
Sonia Tandon
Michele Paine McCullough
Yunchuan Kong
Sarah Kabbani
Muktha S. Natrajan
Yongxian Xu
Yerun Zhu
Dongli Wang
Jesse O’Shea
Amy Sherman
Tianwei Yu
Sebastien Henry
Devin McAllister
Daniel Stadlbauer
Surender Khurana
Hana Golding
Florian Krammer
Mark J. Mulligan
Mark R. Prausnitz
author_facet Nadine G. Rouphael
Lilin Lai
Sonia Tandon
Michele Paine McCullough
Yunchuan Kong
Sarah Kabbani
Muktha S. Natrajan
Yongxian Xu
Yerun Zhu
Dongli Wang
Jesse O’Shea
Amy Sherman
Tianwei Yu
Sebastien Henry
Devin McAllister
Daniel Stadlbauer
Surender Khurana
Hana Golding
Florian Krammer
Mark J. Mulligan
Mark R. Prausnitz
author_sort Nadine G. Rouphael
title Immunologic mechanisms of seasonal influenza vaccination administered by microneedle patch from a randomized phase I trial
title_short Immunologic mechanisms of seasonal influenza vaccination administered by microneedle patch from a randomized phase I trial
title_full Immunologic mechanisms of seasonal influenza vaccination administered by microneedle patch from a randomized phase I trial
title_fullStr Immunologic mechanisms of seasonal influenza vaccination administered by microneedle patch from a randomized phase I trial
title_full_unstemmed Immunologic mechanisms of seasonal influenza vaccination administered by microneedle patch from a randomized phase I trial
title_sort immunologic mechanisms of seasonal influenza vaccination administered by microneedle patch from a randomized phase i trial
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/5b49040c2002496f8128ac3623836663
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