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Pulmonary Conventional Type 1 Langerin-Expressing Dendritic Cells Play a Role in Impairing Early Protective Immune Response against Cryptococcus neoformans Infection in Mice

Lung dendritic cells (DC) are powerful antigen-presenting cells constituted by various subpopulations that differ in terms of their function and origin and differentially regulate cell-mediated antifungal immunity. The lung is the primary target organ of Cryptococcus neoformans and C. gattii infecti...

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Autores principales: Guasconi, Lorena, Beccacece, Ignacio, Volpini, Ximena, Burstein, Verónica L., Mena, Cristian J., Silvane, Leonardo, Almeida, Mariel A., Musri, Melina Mara, Cervi, Laura, Chiapello, Laura S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410147/
https://www.ncbi.nlm.nih.gov/pubmed/36012781
http://dx.doi.org/10.3390/jof8080792
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author Guasconi, Lorena
Beccacece, Ignacio
Volpini, Ximena
Burstein, Verónica L.
Mena, Cristian J.
Silvane, Leonardo
Almeida, Mariel A.
Musri, Melina Mara
Cervi, Laura
Chiapello, Laura S.
author_facet Guasconi, Lorena
Beccacece, Ignacio
Volpini, Ximena
Burstein, Verónica L.
Mena, Cristian J.
Silvane, Leonardo
Almeida, Mariel A.
Musri, Melina Mara
Cervi, Laura
Chiapello, Laura S.
author_sort Guasconi, Lorena
collection PubMed
description Lung dendritic cells (DC) are powerful antigen-presenting cells constituted by various subpopulations that differ in terms of their function and origin and differentially regulate cell-mediated antifungal immunity. The lung is the primary target organ of Cryptococcus neoformans and C. gattii infections, which makes it essential in the establishment of the first line of anti-cryptococcal defense. However, the lung-specific dynamics and function of DC subsets are poorly understood in cryptococcosis. In this study, we provide evidence for the in vivo function of a conventional langerin-expressing DC1 dendritic cell (LangDC1) population during the first week of intratracheal C. neoformans infection in mice. By using conditional depletion of LangDC1 after diphtheria toxin treatment of LangDTREGFP mice, we demonstrate that these animals better control the fungal infection and produce type 1 and 17 cytokines in the context of a type 2 immune response, favoring a predominance of iNOS over arginase-1 expression by pulmonary cells. Our results suggest that LangDC1 cells play a role in impairing immune response for the clearance of C. neoformans in the early stage of pulmonary infection.
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spelling pubmed-94101472022-08-26 Pulmonary Conventional Type 1 Langerin-Expressing Dendritic Cells Play a Role in Impairing Early Protective Immune Response against Cryptococcus neoformans Infection in Mice Guasconi, Lorena Beccacece, Ignacio Volpini, Ximena Burstein, Verónica L. Mena, Cristian J. Silvane, Leonardo Almeida, Mariel A. Musri, Melina Mara Cervi, Laura Chiapello, Laura S. J Fungi (Basel) Communication Lung dendritic cells (DC) are powerful antigen-presenting cells constituted by various subpopulations that differ in terms of their function and origin and differentially regulate cell-mediated antifungal immunity. The lung is the primary target organ of Cryptococcus neoformans and C. gattii infections, which makes it essential in the establishment of the first line of anti-cryptococcal defense. However, the lung-specific dynamics and function of DC subsets are poorly understood in cryptococcosis. In this study, we provide evidence for the in vivo function of a conventional langerin-expressing DC1 dendritic cell (LangDC1) population during the first week of intratracheal C. neoformans infection in mice. By using conditional depletion of LangDC1 after diphtheria toxin treatment of LangDTREGFP mice, we demonstrate that these animals better control the fungal infection and produce type 1 and 17 cytokines in the context of a type 2 immune response, favoring a predominance of iNOS over arginase-1 expression by pulmonary cells. Our results suggest that LangDC1 cells play a role in impairing immune response for the clearance of C. neoformans in the early stage of pulmonary infection. MDPI 2022-07-28 /pmc/articles/PMC9410147/ /pubmed/36012781 http://dx.doi.org/10.3390/jof8080792 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Guasconi, Lorena
Beccacece, Ignacio
Volpini, Ximena
Burstein, Verónica L.
Mena, Cristian J.
Silvane, Leonardo
Almeida, Mariel A.
Musri, Melina Mara
Cervi, Laura
Chiapello, Laura S.
Pulmonary Conventional Type 1 Langerin-Expressing Dendritic Cells Play a Role in Impairing Early Protective Immune Response against Cryptococcus neoformans Infection in Mice
title Pulmonary Conventional Type 1 Langerin-Expressing Dendritic Cells Play a Role in Impairing Early Protective Immune Response against Cryptococcus neoformans Infection in Mice
title_full Pulmonary Conventional Type 1 Langerin-Expressing Dendritic Cells Play a Role in Impairing Early Protective Immune Response against Cryptococcus neoformans Infection in Mice
title_fullStr Pulmonary Conventional Type 1 Langerin-Expressing Dendritic Cells Play a Role in Impairing Early Protective Immune Response against Cryptococcus neoformans Infection in Mice
title_full_unstemmed Pulmonary Conventional Type 1 Langerin-Expressing Dendritic Cells Play a Role in Impairing Early Protective Immune Response against Cryptococcus neoformans Infection in Mice
title_short Pulmonary Conventional Type 1 Langerin-Expressing Dendritic Cells Play a Role in Impairing Early Protective Immune Response against Cryptococcus neoformans Infection in Mice
title_sort pulmonary conventional type 1 langerin-expressing dendritic cells play a role in impairing early protective immune response against cryptococcus neoformans infection in mice
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410147/
https://www.ncbi.nlm.nih.gov/pubmed/36012781
http://dx.doi.org/10.3390/jof8080792
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