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Antiviral Activity of Tannic Acid Modified Silver Nanoparticles: Potential to Activate Immune Response in Herpes Genitalis

(1) Background: Tannic acid is a plant-derived polyphenol showing antiviral activity mainly because of an interference with the viral adsorption. In this work, we tested whether the modification of silver nanoparticles with tannic acid (TA-AgNPs) can provide a microbicide with additional adjuvant pr...

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Autores principales: Orłowski, Piotr, Kowalczyk, Andrzej, Tomaszewska, Emilia, Ranoszek-Soliwoda, Katarzyna, Węgrzyn, Agnieszka, Grzesiak, Jakub, Celichowski, Grzegorz, Grobelny, Jarosław, Eriksson, Kristina, Krzyzowska, Malgorzata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6213294/
https://www.ncbi.nlm.nih.gov/pubmed/30261662
http://dx.doi.org/10.3390/v10100524
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author Orłowski, Piotr
Kowalczyk, Andrzej
Tomaszewska, Emilia
Ranoszek-Soliwoda, Katarzyna
Węgrzyn, Agnieszka
Grzesiak, Jakub
Celichowski, Grzegorz
Grobelny, Jarosław
Eriksson, Kristina
Krzyzowska, Malgorzata
author_facet Orłowski, Piotr
Kowalczyk, Andrzej
Tomaszewska, Emilia
Ranoszek-Soliwoda, Katarzyna
Węgrzyn, Agnieszka
Grzesiak, Jakub
Celichowski, Grzegorz
Grobelny, Jarosław
Eriksson, Kristina
Krzyzowska, Malgorzata
author_sort Orłowski, Piotr
collection PubMed
description (1) Background: Tannic acid is a plant-derived polyphenol showing antiviral activity mainly because of an interference with the viral adsorption. In this work, we tested whether the modification of silver nanoparticles with tannic acid (TA-AgNPs) can provide a microbicide with additional adjuvant properties to treat genital herpes infection. (2) Methods: The mouse model of the vaginal herpes simplex virus 2 (HSV-2) infection was used to test immune responses after treatment of the primary infection with TA-AgNPs, and later, after a re-challenge with the virus. (3) Results: The mice treated intravaginally with TA-AgNPs showed better clinical scores and lower virus titers in the vaginal tissues soon after treatment. Following a re-challenge, the vaginal tissues treated with TA-AgNPs showed a significant increase in the percentages of IFN-gamma+ CD8+ T-cells, activated B cells, and plasma cells, while the spleens contained significantly higher percentages of IFN-gamma+ NK cells and effector-memory CD8+ T cells in comparison to NaCl-treated group. TA-AgNPs-treated animals also showed significantly better titers of anti-HSV-2 neutralization antibodies in sera; and (4) Conclusions: Our findings suggest that TA-AgNPs sized 33 nm can be an effective anti-viral microbicide to be applied upon the mucosal tissues with additional adjuvant properties enhancing an anti-HSV-2 immune response following secondary challenge.
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spelling pubmed-62132942018-11-09 Antiviral Activity of Tannic Acid Modified Silver Nanoparticles: Potential to Activate Immune Response in Herpes Genitalis Orłowski, Piotr Kowalczyk, Andrzej Tomaszewska, Emilia Ranoszek-Soliwoda, Katarzyna Węgrzyn, Agnieszka Grzesiak, Jakub Celichowski, Grzegorz Grobelny, Jarosław Eriksson, Kristina Krzyzowska, Malgorzata Viruses Article (1) Background: Tannic acid is a plant-derived polyphenol showing antiviral activity mainly because of an interference with the viral adsorption. In this work, we tested whether the modification of silver nanoparticles with tannic acid (TA-AgNPs) can provide a microbicide with additional adjuvant properties to treat genital herpes infection. (2) Methods: The mouse model of the vaginal herpes simplex virus 2 (HSV-2) infection was used to test immune responses after treatment of the primary infection with TA-AgNPs, and later, after a re-challenge with the virus. (3) Results: The mice treated intravaginally with TA-AgNPs showed better clinical scores and lower virus titers in the vaginal tissues soon after treatment. Following a re-challenge, the vaginal tissues treated with TA-AgNPs showed a significant increase in the percentages of IFN-gamma+ CD8+ T-cells, activated B cells, and plasma cells, while the spleens contained significantly higher percentages of IFN-gamma+ NK cells and effector-memory CD8+ T cells in comparison to NaCl-treated group. TA-AgNPs-treated animals also showed significantly better titers of anti-HSV-2 neutralization antibodies in sera; and (4) Conclusions: Our findings suggest that TA-AgNPs sized 33 nm can be an effective anti-viral microbicide to be applied upon the mucosal tissues with additional adjuvant properties enhancing an anti-HSV-2 immune response following secondary challenge. MDPI 2018-09-26 /pmc/articles/PMC6213294/ /pubmed/30261662 http://dx.doi.org/10.3390/v10100524 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Orłowski, Piotr
Kowalczyk, Andrzej
Tomaszewska, Emilia
Ranoszek-Soliwoda, Katarzyna
Węgrzyn, Agnieszka
Grzesiak, Jakub
Celichowski, Grzegorz
Grobelny, Jarosław
Eriksson, Kristina
Krzyzowska, Malgorzata
Antiviral Activity of Tannic Acid Modified Silver Nanoparticles: Potential to Activate Immune Response in Herpes Genitalis
title Antiviral Activity of Tannic Acid Modified Silver Nanoparticles: Potential to Activate Immune Response in Herpes Genitalis
title_full Antiviral Activity of Tannic Acid Modified Silver Nanoparticles: Potential to Activate Immune Response in Herpes Genitalis
title_fullStr Antiviral Activity of Tannic Acid Modified Silver Nanoparticles: Potential to Activate Immune Response in Herpes Genitalis
title_full_unstemmed Antiviral Activity of Tannic Acid Modified Silver Nanoparticles: Potential to Activate Immune Response in Herpes Genitalis
title_short Antiviral Activity of Tannic Acid Modified Silver Nanoparticles: Potential to Activate Immune Response in Herpes Genitalis
title_sort antiviral activity of tannic acid modified silver nanoparticles: potential to activate immune response in herpes genitalis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6213294/
https://www.ncbi.nlm.nih.gov/pubmed/30261662
http://dx.doi.org/10.3390/v10100524
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