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Transmission of Zika virus by dendritic cell subsets in skin and vaginal mucosa
Zika virus is a member of the Flaviviridae family that has caused recent outbreaks associated with neurological malformations. Transmission of Zika virus occurs primarily via mosquito bite but also via sexual contact. Dendritic cells (DCs) and Langerhans cells (LCs) are important antigen presenting...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025456/ https://www.ncbi.nlm.nih.gov/pubmed/36949942 http://dx.doi.org/10.3389/fimmu.2023.1125565 |
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author | Eder, Julia Zijlstra-Willems, Esther Koen, Gerrit Kootstra, Neeltje A. Wolthers, Katja C. Geijtenbeek, Teunis B. |
author_facet | Eder, Julia Zijlstra-Willems, Esther Koen, Gerrit Kootstra, Neeltje A. Wolthers, Katja C. Geijtenbeek, Teunis B. |
author_sort | Eder, Julia |
collection | PubMed |
description | Zika virus is a member of the Flaviviridae family that has caused recent outbreaks associated with neurological malformations. Transmission of Zika virus occurs primarily via mosquito bite but also via sexual contact. Dendritic cells (DCs) and Langerhans cells (LCs) are important antigen presenting cells in skin and vaginal mucosa and paramount to induce antiviral immunity. To date, little is known about the first cells targeted by Zika virus in these tissues as well as subsequent dissemination of the virus to other target cells. We therefore investigated the role of DCs and LCs in Zika virus infection. Human monocyte derived DCs (moDCs) were isolated from blood and primary immature LCs were obtained from human skin and vaginal explants. Zika virus exposure to moDCs but not skin and vaginal LCs induced Type I Interferon responses. Zika virus efficiently infected moDCs but neither epidermal nor vaginal LCs became infected. Infection of a human full skin model showed that DC-SIGN expressing dermal DCs are preferentially infected over langerin+ LCs. Notably, not only moDCs but also skin and vaginal LCs efficiently transmitted Zika virus to target cells. Transmission by LCs was independent of direct infection of LCs. These data suggest that DCs and LCs are among the first target cells for Zika virus not only in the skin but also the genital tract. The role of vaginal LCs in dissemination of Zika virus from the vaginal mucosa further emphasizes the threat of sexual transmission and supports the investigation of prophylaxes that go beyond mosquito control. |
format | Online Article Text |
id | pubmed-10025456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100254562023-03-21 Transmission of Zika virus by dendritic cell subsets in skin and vaginal mucosa Eder, Julia Zijlstra-Willems, Esther Koen, Gerrit Kootstra, Neeltje A. Wolthers, Katja C. Geijtenbeek, Teunis B. Front Immunol Immunology Zika virus is a member of the Flaviviridae family that has caused recent outbreaks associated with neurological malformations. Transmission of Zika virus occurs primarily via mosquito bite but also via sexual contact. Dendritic cells (DCs) and Langerhans cells (LCs) are important antigen presenting cells in skin and vaginal mucosa and paramount to induce antiviral immunity. To date, little is known about the first cells targeted by Zika virus in these tissues as well as subsequent dissemination of the virus to other target cells. We therefore investigated the role of DCs and LCs in Zika virus infection. Human monocyte derived DCs (moDCs) were isolated from blood and primary immature LCs were obtained from human skin and vaginal explants. Zika virus exposure to moDCs but not skin and vaginal LCs induced Type I Interferon responses. Zika virus efficiently infected moDCs but neither epidermal nor vaginal LCs became infected. Infection of a human full skin model showed that DC-SIGN expressing dermal DCs are preferentially infected over langerin+ LCs. Notably, not only moDCs but also skin and vaginal LCs efficiently transmitted Zika virus to target cells. Transmission by LCs was independent of direct infection of LCs. These data suggest that DCs and LCs are among the first target cells for Zika virus not only in the skin but also the genital tract. The role of vaginal LCs in dissemination of Zika virus from the vaginal mucosa further emphasizes the threat of sexual transmission and supports the investigation of prophylaxes that go beyond mosquito control. Frontiers Media S.A. 2023-03-06 /pmc/articles/PMC10025456/ /pubmed/36949942 http://dx.doi.org/10.3389/fimmu.2023.1125565 Text en Copyright © 2023 Eder, Zijlstra-Willems, Koen, Kootstra, Wolthers and Geijtenbeek https://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) and the copyright owner(s) 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 Eder, Julia Zijlstra-Willems, Esther Koen, Gerrit Kootstra, Neeltje A. Wolthers, Katja C. Geijtenbeek, Teunis B. Transmission of Zika virus by dendritic cell subsets in skin and vaginal mucosa |
title | Transmission of Zika virus by dendritic cell subsets in skin and vaginal mucosa |
title_full | Transmission of Zika virus by dendritic cell subsets in skin and vaginal mucosa |
title_fullStr | Transmission of Zika virus by dendritic cell subsets in skin and vaginal mucosa |
title_full_unstemmed | Transmission of Zika virus by dendritic cell subsets in skin and vaginal mucosa |
title_short | Transmission of Zika virus by dendritic cell subsets in skin and vaginal mucosa |
title_sort | transmission of zika virus by dendritic cell subsets in skin and vaginal mucosa |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025456/ https://www.ncbi.nlm.nih.gov/pubmed/36949942 http://dx.doi.org/10.3389/fimmu.2023.1125565 |
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