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Clinical study of transcutaneous vaccination using a hydrogel patch for tetanus and diphtheria

Transcutaneous immunization (TCI) is a non-invasive and easy-to-use vaccination method. We demonstrated the efficacy and safety of a transcutaneous vaccine formulation using a hydrogel patch in animal experiments. In the present study, we performed a clinical study to apply our TCI formulation for v...

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Autores principales: Hirobe, Sachiko, Matsuo, Kazuhiko, Quan, Ying-Shu, Kamiyama, Fumio, Morito, Hironori, Asada, Hideo, Takaya, Yusuke, Mukai, Yohei, Okada, Naoki, Nakagawa, Shinsaku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126733/
https://www.ncbi.nlm.nih.gov/pubmed/22230592
http://dx.doi.org/10.1016/j.vaccine.2011.12.130
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author Hirobe, Sachiko
Matsuo, Kazuhiko
Quan, Ying-Shu
Kamiyama, Fumio
Morito, Hironori
Asada, Hideo
Takaya, Yusuke
Mukai, Yohei
Okada, Naoki
Nakagawa, Shinsaku
author_facet Hirobe, Sachiko
Matsuo, Kazuhiko
Quan, Ying-Shu
Kamiyama, Fumio
Morito, Hironori
Asada, Hideo
Takaya, Yusuke
Mukai, Yohei
Okada, Naoki
Nakagawa, Shinsaku
author_sort Hirobe, Sachiko
collection PubMed
description Transcutaneous immunization (TCI) is a non-invasive and easy-to-use vaccination method. We demonstrated the efficacy and safety of a transcutaneous vaccine formulation using a hydrogel patch in animal experiments. In the present study, we performed a clinical study to apply our TCI formulation for vaccination against tetanus and diphtheria in human. The TCI device was a hydrogel patch (antigen-free) applied to the left brachial medial skin of 22 healthy volunteers for 48 h. Next, the hydrogel patch, containing 2 mg tetanus toxoid (TT) and 2 mg diphtheria toxoid (DT) as the TCI formulation, was applied to 27 healthy volunteers for 24 h and some volunteers were vaccinated again by TCI formulation. For safety assessment, the patch application site was observed to assess local adverse events, and systemic adverse events were determined by a blood test. The antigen-free hydrogel patch and TCI formulation containing TT and DT did not induce local or systemic severe adverse events. For vaccine efficacy estimation, toxoid-specific serum antibody titers were determined by ELISA and the toxin-neutralizing activity of the induced antibody was evaluated in a passive-challenge experiment. The anti-TT IgG titer and the anti-DT IgG titer increased, and a significant effect was detected by paired t-test. The antibody titers were maintained at higher level than that before vaccination for at least 1 year. Moreover, toxoid-specific antibodies were produced by the second vaccination in some subjects. Antibodies induced by application of the TCI formulation neutralized the toxin and prevented toxic death in mice. In addition, changes in the skin condition due to application of the TCI formulation were observed under in vivo confocal Raman spectroscopy. The amount of water and patch components in the stratum corneum increased after application of the TCI formulation, suggesting that the change in the skin condition was related to antigen penetration. These data indicate that this easy-to-use TCI system induces an immune response without severe adverse reactions in humans. This easy-to-use and safe TCI formulation enables mass treatment in an outbreak setting and increased vaccination rates in developing countries, and will greatly contribute to worldwide countermeasures against infectious diseases.
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spelling pubmed-71267332020-04-08 Clinical study of transcutaneous vaccination using a hydrogel patch for tetanus and diphtheria Hirobe, Sachiko Matsuo, Kazuhiko Quan, Ying-Shu Kamiyama, Fumio Morito, Hironori Asada, Hideo Takaya, Yusuke Mukai, Yohei Okada, Naoki Nakagawa, Shinsaku Vaccine Article Transcutaneous immunization (TCI) is a non-invasive and easy-to-use vaccination method. We demonstrated the efficacy and safety of a transcutaneous vaccine formulation using a hydrogel patch in animal experiments. In the present study, we performed a clinical study to apply our TCI formulation for vaccination against tetanus and diphtheria in human. The TCI device was a hydrogel patch (antigen-free) applied to the left brachial medial skin of 22 healthy volunteers for 48 h. Next, the hydrogel patch, containing 2 mg tetanus toxoid (TT) and 2 mg diphtheria toxoid (DT) as the TCI formulation, was applied to 27 healthy volunteers for 24 h and some volunteers were vaccinated again by TCI formulation. For safety assessment, the patch application site was observed to assess local adverse events, and systemic adverse events were determined by a blood test. The antigen-free hydrogel patch and TCI formulation containing TT and DT did not induce local or systemic severe adverse events. For vaccine efficacy estimation, toxoid-specific serum antibody titers were determined by ELISA and the toxin-neutralizing activity of the induced antibody was evaluated in a passive-challenge experiment. The anti-TT IgG titer and the anti-DT IgG titer increased, and a significant effect was detected by paired t-test. The antibody titers were maintained at higher level than that before vaccination for at least 1 year. Moreover, toxoid-specific antibodies were produced by the second vaccination in some subjects. Antibodies induced by application of the TCI formulation neutralized the toxin and prevented toxic death in mice. In addition, changes in the skin condition due to application of the TCI formulation were observed under in vivo confocal Raman spectroscopy. The amount of water and patch components in the stratum corneum increased after application of the TCI formulation, suggesting that the change in the skin condition was related to antigen penetration. These data indicate that this easy-to-use TCI system induces an immune response without severe adverse reactions in humans. This easy-to-use and safe TCI formulation enables mass treatment in an outbreak setting and increased vaccination rates in developing countries, and will greatly contribute to worldwide countermeasures against infectious diseases. Elsevier Ltd. 2012-02-27 2012-01-08 /pmc/articles/PMC7126733/ /pubmed/22230592 http://dx.doi.org/10.1016/j.vaccine.2011.12.130 Text en Copyright © 2012 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Hirobe, Sachiko
Matsuo, Kazuhiko
Quan, Ying-Shu
Kamiyama, Fumio
Morito, Hironori
Asada, Hideo
Takaya, Yusuke
Mukai, Yohei
Okada, Naoki
Nakagawa, Shinsaku
Clinical study of transcutaneous vaccination using a hydrogel patch for tetanus and diphtheria
title Clinical study of transcutaneous vaccination using a hydrogel patch for tetanus and diphtheria
title_full Clinical study of transcutaneous vaccination using a hydrogel patch for tetanus and diphtheria
title_fullStr Clinical study of transcutaneous vaccination using a hydrogel patch for tetanus and diphtheria
title_full_unstemmed Clinical study of transcutaneous vaccination using a hydrogel patch for tetanus and diphtheria
title_short Clinical study of transcutaneous vaccination using a hydrogel patch for tetanus and diphtheria
title_sort clinical study of transcutaneous vaccination using a hydrogel patch for tetanus and diphtheria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126733/
https://www.ncbi.nlm.nih.gov/pubmed/22230592
http://dx.doi.org/10.1016/j.vaccine.2011.12.130
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