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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
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.
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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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