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Antifungals influence the immune-related transcriptomic landscape of human monocytes after Aspergillus fumigatus infection

The heterogeneity of clinical responses to antifungals in aspergillosis is partially understood. We hypothesized that besides direct antifungal effects, these discrepancies may be related to different immunomodulatory profiles. Human THP-1 monocytes were coincubated in vitro with Aspergillus fumigat...

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Autores principales: Henry, Benoît, Klement, William, Gohir, Wajiha, Aguilar, Claire, Husain, Shahid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931103/
https://www.ncbi.nlm.nih.gov/pubmed/35301416
http://dx.doi.org/10.1038/s41598-022-08738-4
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author Henry, Benoît
Klement, William
Gohir, Wajiha
Aguilar, Claire
Husain, Shahid
author_facet Henry, Benoît
Klement, William
Gohir, Wajiha
Aguilar, Claire
Husain, Shahid
author_sort Henry, Benoît
collection PubMed
description The heterogeneity of clinical responses to antifungals in aspergillosis is partially understood. We hypothesized that besides direct antifungal effects, these discrepancies may be related to different immunomodulatory profiles. Human THP-1 monocytes were coincubated in vitro with Aspergillus fumigatus and variable concentrations of voriconazole (0.5, 1 and 2 mg/l), caspofungin (1 and 2 mg/l), amphotericin B deoxycholate (0.25, 0.5 and 1 mg/l) and liposomal amphotericin B (1, 2 and 3 mg/l). After 6 h of coincubation, total cellular RNA was extracted, converted into cDNA, and transcription of 84 genes involved in antifungal immunity was measured through RT-qPCR. The presence of A. fumigatus was the main driver of the global immune-related transcriptomic response. After Aspergillus infection, thirty genes were upregulated, while 19 genes were downregulated. Discrepancies across antifungals were also evident; voriconazole-containing conditions showed similar reaction to natural infection, while the use of liposomal Amphotericin B significantly decreased the inflammatory response. Chemokines (notably CCL20 and CXCL2) and pro-inflammatory cytokines (IL1A, IL1B, IL23, G-CSF) exhibited the most pronounced differences across antifungals. Pattern recognition receptors and adaptor protein transcription were minimally affected. Protein–protein-interaction network analysis showed that IL23A played a dominant role in upregulated genes. Pathway enrichment analysis indicated that cytokine-cytokine receptor integration, TNF signaling pathways and Toll-like receptor pathways were highly involved. This exploratory study confirms the heterogeneous immunomodulatory role of antifungals. Overall, voriconazole appears to maintain an early pro-inflammatory response seen in natural infection. Assessment of immunomodulatory response with clinical response may provide a better rationale for differences observed across antifungals.
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spelling pubmed-89311032022-03-21 Antifungals influence the immune-related transcriptomic landscape of human monocytes after Aspergillus fumigatus infection Henry, Benoît Klement, William Gohir, Wajiha Aguilar, Claire Husain, Shahid Sci Rep Article The heterogeneity of clinical responses to antifungals in aspergillosis is partially understood. We hypothesized that besides direct antifungal effects, these discrepancies may be related to different immunomodulatory profiles. Human THP-1 monocytes were coincubated in vitro with Aspergillus fumigatus and variable concentrations of voriconazole (0.5, 1 and 2 mg/l), caspofungin (1 and 2 mg/l), amphotericin B deoxycholate (0.25, 0.5 and 1 mg/l) and liposomal amphotericin B (1, 2 and 3 mg/l). After 6 h of coincubation, total cellular RNA was extracted, converted into cDNA, and transcription of 84 genes involved in antifungal immunity was measured through RT-qPCR. The presence of A. fumigatus was the main driver of the global immune-related transcriptomic response. After Aspergillus infection, thirty genes were upregulated, while 19 genes were downregulated. Discrepancies across antifungals were also evident; voriconazole-containing conditions showed similar reaction to natural infection, while the use of liposomal Amphotericin B significantly decreased the inflammatory response. Chemokines (notably CCL20 and CXCL2) and pro-inflammatory cytokines (IL1A, IL1B, IL23, G-CSF) exhibited the most pronounced differences across antifungals. Pattern recognition receptors and adaptor protein transcription were minimally affected. Protein–protein-interaction network analysis showed that IL23A played a dominant role in upregulated genes. Pathway enrichment analysis indicated that cytokine-cytokine receptor integration, TNF signaling pathways and Toll-like receptor pathways were highly involved. This exploratory study confirms the heterogeneous immunomodulatory role of antifungals. Overall, voriconazole appears to maintain an early pro-inflammatory response seen in natural infection. Assessment of immunomodulatory response with clinical response may provide a better rationale for differences observed across antifungals. Nature Publishing Group UK 2022-03-17 /pmc/articles/PMC8931103/ /pubmed/35301416 http://dx.doi.org/10.1038/s41598-022-08738-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Henry, Benoît
Klement, William
Gohir, Wajiha
Aguilar, Claire
Husain, Shahid
Antifungals influence the immune-related transcriptomic landscape of human monocytes after Aspergillus fumigatus infection
title Antifungals influence the immune-related transcriptomic landscape of human monocytes after Aspergillus fumigatus infection
title_full Antifungals influence the immune-related transcriptomic landscape of human monocytes after Aspergillus fumigatus infection
title_fullStr Antifungals influence the immune-related transcriptomic landscape of human monocytes after Aspergillus fumigatus infection
title_full_unstemmed Antifungals influence the immune-related transcriptomic landscape of human monocytes after Aspergillus fumigatus infection
title_short Antifungals influence the immune-related transcriptomic landscape of human monocytes after Aspergillus fumigatus infection
title_sort antifungals influence the immune-related transcriptomic landscape of human monocytes after aspergillus fumigatus infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931103/
https://www.ncbi.nlm.nih.gov/pubmed/35301416
http://dx.doi.org/10.1038/s41598-022-08738-4
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