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Nasal Immunization Confers High Avidity Neutralizing Antibody Response and Immunity to Primary and Recurrent Genital Herpes in Guinea Pigs

Genital herpes is one of the most prevalent sexually transmitted infections in both the developing and developed world. Following infection, individuals experience life-long latency associated with sporadic ulcerative outbreaks. Despite many efforts, no vaccine has yet been licensed for human use. H...

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Autores principales: Persson, Josefine, Zhang, Yuan, Olafsdottir, Thorunn A., Thörn, Karolina, Cairns, Tina M., Wegmann, Frank, Sattentau, Quentin J., Eisenberg, Roselyn J., Cohen, Gary H., Harandi, Ali M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5183738/
https://www.ncbi.nlm.nih.gov/pubmed/28082979
http://dx.doi.org/10.3389/fimmu.2016.00640
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author Persson, Josefine
Zhang, Yuan
Olafsdottir, Thorunn A.
Thörn, Karolina
Cairns, Tina M.
Wegmann, Frank
Sattentau, Quentin J.
Eisenberg, Roselyn J.
Cohen, Gary H.
Harandi, Ali M.
author_facet Persson, Josefine
Zhang, Yuan
Olafsdottir, Thorunn A.
Thörn, Karolina
Cairns, Tina M.
Wegmann, Frank
Sattentau, Quentin J.
Eisenberg, Roselyn J.
Cohen, Gary H.
Harandi, Ali M.
author_sort Persson, Josefine
collection PubMed
description Genital herpes is one of the most prevalent sexually transmitted infections in both the developing and developed world. Following infection, individuals experience life-long latency associated with sporadic ulcerative outbreaks. Despite many efforts, no vaccine has yet been licensed for human use. Herein, we demonstrated that nasal immunization with an adjuvanted HSV-2 gD envelope protein mounts significant protection to primary infection as well as the establishment of latency and recurrent genital herpes in guinea pigs. Nasal immunization was shown to elicit specific T cell proliferative and IFN-γ responses as well as systemic and vaginal gD-specific IgG antibody (Ab) responses. Furthermore, systemic IgG Abs displayed potent HSV-2 neutralizing properties and high avidity. By employing a competitive surface plasmon resonance (SPR) analysis combined with a battery of known gD-specific neutralizing monoclonal Abs (MAbs), we showed that nasal immunization generated IgG Abs directed to two major discontinuous neutralizing epitopes of gD. These results highlight the potential of nasal immunization with an adjuvanted HSV-2 envelope protein for induction of protective immunity to primary and recurrent genital herpes.
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spelling pubmed-51837382017-01-12 Nasal Immunization Confers High Avidity Neutralizing Antibody Response and Immunity to Primary and Recurrent Genital Herpes in Guinea Pigs Persson, Josefine Zhang, Yuan Olafsdottir, Thorunn A. Thörn, Karolina Cairns, Tina M. Wegmann, Frank Sattentau, Quentin J. Eisenberg, Roselyn J. Cohen, Gary H. Harandi, Ali M. Front Immunol Immunology Genital herpes is one of the most prevalent sexually transmitted infections in both the developing and developed world. Following infection, individuals experience life-long latency associated with sporadic ulcerative outbreaks. Despite many efforts, no vaccine has yet been licensed for human use. Herein, we demonstrated that nasal immunization with an adjuvanted HSV-2 gD envelope protein mounts significant protection to primary infection as well as the establishment of latency and recurrent genital herpes in guinea pigs. Nasal immunization was shown to elicit specific T cell proliferative and IFN-γ responses as well as systemic and vaginal gD-specific IgG antibody (Ab) responses. Furthermore, systemic IgG Abs displayed potent HSV-2 neutralizing properties and high avidity. By employing a competitive surface plasmon resonance (SPR) analysis combined with a battery of known gD-specific neutralizing monoclonal Abs (MAbs), we showed that nasal immunization generated IgG Abs directed to two major discontinuous neutralizing epitopes of gD. These results highlight the potential of nasal immunization with an adjuvanted HSV-2 envelope protein for induction of protective immunity to primary and recurrent genital herpes. Frontiers Media S.A. 2016-12-26 /pmc/articles/PMC5183738/ /pubmed/28082979 http://dx.doi.org/10.3389/fimmu.2016.00640 Text en Copyright © 2016 Persson, Zhang, Olafsdottir, Thörn, Cairns, Wegmann, Sattentau, Eisenberg, Cohen and Harandi. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Persson, Josefine
Zhang, Yuan
Olafsdottir, Thorunn A.
Thörn, Karolina
Cairns, Tina M.
Wegmann, Frank
Sattentau, Quentin J.
Eisenberg, Roselyn J.
Cohen, Gary H.
Harandi, Ali M.
Nasal Immunization Confers High Avidity Neutralizing Antibody Response and Immunity to Primary and Recurrent Genital Herpes in Guinea Pigs
title Nasal Immunization Confers High Avidity Neutralizing Antibody Response and Immunity to Primary and Recurrent Genital Herpes in Guinea Pigs
title_full Nasal Immunization Confers High Avidity Neutralizing Antibody Response and Immunity to Primary and Recurrent Genital Herpes in Guinea Pigs
title_fullStr Nasal Immunization Confers High Avidity Neutralizing Antibody Response and Immunity to Primary and Recurrent Genital Herpes in Guinea Pigs
title_full_unstemmed Nasal Immunization Confers High Avidity Neutralizing Antibody Response and Immunity to Primary and Recurrent Genital Herpes in Guinea Pigs
title_short Nasal Immunization Confers High Avidity Neutralizing Antibody Response and Immunity to Primary and Recurrent Genital Herpes in Guinea Pigs
title_sort nasal immunization confers high avidity neutralizing antibody response and immunity to primary and recurrent genital herpes in guinea pigs
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5183738/
https://www.ncbi.nlm.nih.gov/pubmed/28082979
http://dx.doi.org/10.3389/fimmu.2016.00640
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