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Dendritic Cells From the Cervical Mucosa Capture and Transfer HIV-1 via Siglec-1
Antigen presenting cells from the cervical mucosa are thought to amplify incoming HIV-1 and spread infection systemically without being productively infected. Yet, the molecular mechanism at the cervical mucosa underlying this viral transmission pathway remains unknown. Here we identified a subset o...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503733/ https://www.ncbi.nlm.nih.gov/pubmed/31114569 http://dx.doi.org/10.3389/fimmu.2019.00825 |
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author | Perez-Zsolt, Daniel Cantero-Pérez, Jon Erkizia, Itziar Benet, Susana Pino, Maria Serra-Peinado, Carla Hernández-Gallego, Alba Castellví, Josep Tapia, Gustavo Arnau-Saz, Vicent Garrido, Julio Tarrats, Antoni Buzón, Maria J. Martinez-Picado, Javier Izquierdo-Useros, Nuria Genescà, Meritxell |
author_facet | Perez-Zsolt, Daniel Cantero-Pérez, Jon Erkizia, Itziar Benet, Susana Pino, Maria Serra-Peinado, Carla Hernández-Gallego, Alba Castellví, Josep Tapia, Gustavo Arnau-Saz, Vicent Garrido, Julio Tarrats, Antoni Buzón, Maria J. Martinez-Picado, Javier Izquierdo-Useros, Nuria Genescà, Meritxell |
author_sort | Perez-Zsolt, Daniel |
collection | PubMed |
description | Antigen presenting cells from the cervical mucosa are thought to amplify incoming HIV-1 and spread infection systemically without being productively infected. Yet, the molecular mechanism at the cervical mucosa underlying this viral transmission pathway remains unknown. Here we identified a subset of HLA-DR(+) CD14(+) CD11c(+) cervical DCs at the lamina propria of the ectocervix and the endocervix that expressed the type-I interferon inducible lectin Siglec-1 (CD169), which promoted viral uptake. In the cervical biopsy of a viremic HIV-1(+) patient, Siglec-1(+) cells harbored HIV-1-containing compartments, demonstrating that in vivo, these cells trap viruses. Ex vivo, a type-I interferon antiviral environment enhanced viral capture and trans-infection via Siglec-1. Nonetheless, HIV-1 transfer via cervical DCs was effectively prevented with antibodies against Siglec-1. Our findings contribute to decipher how cervical DCs may boost HIV-1 replication and promote systemic viral spread from the cervical mucosa, and highlight the importance of including inhibitors against Siglec-1 in microbicidal strategies. |
format | Online Article Text |
id | pubmed-6503733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65037332019-05-21 Dendritic Cells From the Cervical Mucosa Capture and Transfer HIV-1 via Siglec-1 Perez-Zsolt, Daniel Cantero-Pérez, Jon Erkizia, Itziar Benet, Susana Pino, Maria Serra-Peinado, Carla Hernández-Gallego, Alba Castellví, Josep Tapia, Gustavo Arnau-Saz, Vicent Garrido, Julio Tarrats, Antoni Buzón, Maria J. Martinez-Picado, Javier Izquierdo-Useros, Nuria Genescà, Meritxell Front Immunol Immunology Antigen presenting cells from the cervical mucosa are thought to amplify incoming HIV-1 and spread infection systemically without being productively infected. Yet, the molecular mechanism at the cervical mucosa underlying this viral transmission pathway remains unknown. Here we identified a subset of HLA-DR(+) CD14(+) CD11c(+) cervical DCs at the lamina propria of the ectocervix and the endocervix that expressed the type-I interferon inducible lectin Siglec-1 (CD169), which promoted viral uptake. In the cervical biopsy of a viremic HIV-1(+) patient, Siglec-1(+) cells harbored HIV-1-containing compartments, demonstrating that in vivo, these cells trap viruses. Ex vivo, a type-I interferon antiviral environment enhanced viral capture and trans-infection via Siglec-1. Nonetheless, HIV-1 transfer via cervical DCs was effectively prevented with antibodies against Siglec-1. Our findings contribute to decipher how cervical DCs may boost HIV-1 replication and promote systemic viral spread from the cervical mucosa, and highlight the importance of including inhibitors against Siglec-1 in microbicidal strategies. Frontiers Media S.A. 2019-04-30 /pmc/articles/PMC6503733/ /pubmed/31114569 http://dx.doi.org/10.3389/fimmu.2019.00825 Text en Copyright © 2019 Perez-Zsolt, Cantero-Pérez, Erkizia, Benet, Pino, Serra-Peinado, Hernández-Gallego, Castellví, Tapia, Arnau-Saz, Garrido, Tarrats, Buzón, Martinez-Picado, Izquierdo-Useros and Genescà. 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) 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 Perez-Zsolt, Daniel Cantero-Pérez, Jon Erkizia, Itziar Benet, Susana Pino, Maria Serra-Peinado, Carla Hernández-Gallego, Alba Castellví, Josep Tapia, Gustavo Arnau-Saz, Vicent Garrido, Julio Tarrats, Antoni Buzón, Maria J. Martinez-Picado, Javier Izquierdo-Useros, Nuria Genescà, Meritxell Dendritic Cells From the Cervical Mucosa Capture and Transfer HIV-1 via Siglec-1 |
title | Dendritic Cells From the Cervical Mucosa Capture and Transfer HIV-1 via Siglec-1 |
title_full | Dendritic Cells From the Cervical Mucosa Capture and Transfer HIV-1 via Siglec-1 |
title_fullStr | Dendritic Cells From the Cervical Mucosa Capture and Transfer HIV-1 via Siglec-1 |
title_full_unstemmed | Dendritic Cells From the Cervical Mucosa Capture and Transfer HIV-1 via Siglec-1 |
title_short | Dendritic Cells From the Cervical Mucosa Capture and Transfer HIV-1 via Siglec-1 |
title_sort | dendritic cells from the cervical mucosa capture and transfer hiv-1 via siglec-1 |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503733/ https://www.ncbi.nlm.nih.gov/pubmed/31114569 http://dx.doi.org/10.3389/fimmu.2019.00825 |
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