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Indoleamine 2,3‐dioxygenase (IDO)‐1 and IDO‐2 activity and severe course of COVID‐19
COVID‐19 is a pandemic with high morbidity and mortality. In an autopsy cohort of COVID‐19 patients, we found extensive accumulation of the tryptophan degradation products 3‐hydroxy‐anthranilic acid and quinolinic acid in the lungs, heart, and brain. This was not related to the expression of the try...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897979/ https://www.ncbi.nlm.nih.gov/pubmed/34859884 http://dx.doi.org/10.1002/path.5842 |
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author | Guo, Lihui Schurink, Bernadette Roos, Eva Nossent, Esther J Duitman, Jan Willem Vlaar, Alexander PJ van der Valk, Paul Vaz, Frédéric M Yeh, Syun‐Ru Geeraerts, Zachary Dijkhuis, Annemiek van Vught, Lonneke Bugiani, Marianna Lutter, René |
author_facet | Guo, Lihui Schurink, Bernadette Roos, Eva Nossent, Esther J Duitman, Jan Willem Vlaar, Alexander PJ van der Valk, Paul Vaz, Frédéric M Yeh, Syun‐Ru Geeraerts, Zachary Dijkhuis, Annemiek van Vught, Lonneke Bugiani, Marianna Lutter, René |
author_sort | Guo, Lihui |
collection | PubMed |
description | COVID‐19 is a pandemic with high morbidity and mortality. In an autopsy cohort of COVID‐19 patients, we found extensive accumulation of the tryptophan degradation products 3‐hydroxy‐anthranilic acid and quinolinic acid in the lungs, heart, and brain. This was not related to the expression of the tryptophan‐catabolizing indoleamine 2,3‐dioxygenase (IDO)‐1, but rather to that of its isoform IDO‐2, which otherwise is expressed rarely. Bioavailability of tryptophan is an absolute requirement for proper cell functioning and synthesis of hormones, whereas its degradation products can cause cell death. Markers of apoptosis and severe cellular stress were associated with IDO‐2 expression in large areas of lung and heart tissue, whereas affected areas in brain were more restricted. Analyses of tissue, cerebrospinal fluid, and sequential plasma samples indicate early initiation of the kynurenine/aryl‐hydrocarbon receptor/IDO‐2 axis as a positive feedback loop, potentially leading to severe COVID‐19 pathology. © 2021 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd on behalf of The Pathological Society of Great Britain and Ireland. |
format | Online Article Text |
id | pubmed-8897979 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-88979792022-03-05 Indoleamine 2,3‐dioxygenase (IDO)‐1 and IDO‐2 activity and severe course of COVID‐19 Guo, Lihui Schurink, Bernadette Roos, Eva Nossent, Esther J Duitman, Jan Willem Vlaar, Alexander PJ van der Valk, Paul Vaz, Frédéric M Yeh, Syun‐Ru Geeraerts, Zachary Dijkhuis, Annemiek van Vught, Lonneke Bugiani, Marianna Lutter, René J Pathol Brief Reports COVID‐19 is a pandemic with high morbidity and mortality. In an autopsy cohort of COVID‐19 patients, we found extensive accumulation of the tryptophan degradation products 3‐hydroxy‐anthranilic acid and quinolinic acid in the lungs, heart, and brain. This was not related to the expression of the tryptophan‐catabolizing indoleamine 2,3‐dioxygenase (IDO)‐1, but rather to that of its isoform IDO‐2, which otherwise is expressed rarely. Bioavailability of tryptophan is an absolute requirement for proper cell functioning and synthesis of hormones, whereas its degradation products can cause cell death. Markers of apoptosis and severe cellular stress were associated with IDO‐2 expression in large areas of lung and heart tissue, whereas affected areas in brain were more restricted. Analyses of tissue, cerebrospinal fluid, and sequential plasma samples indicate early initiation of the kynurenine/aryl‐hydrocarbon receptor/IDO‐2 axis as a positive feedback loop, potentially leading to severe COVID‐19 pathology. © 2021 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd on behalf of The Pathological Society of Great Britain and Ireland. John Wiley & Sons, Ltd 2022-01-10 2022-03 /pmc/articles/PMC8897979/ /pubmed/34859884 http://dx.doi.org/10.1002/path.5842 Text en © 2021 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd on behalf of The Pathological Society of Great Britain and Ireland. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Brief Reports Guo, Lihui Schurink, Bernadette Roos, Eva Nossent, Esther J Duitman, Jan Willem Vlaar, Alexander PJ van der Valk, Paul Vaz, Frédéric M Yeh, Syun‐Ru Geeraerts, Zachary Dijkhuis, Annemiek van Vught, Lonneke Bugiani, Marianna Lutter, René Indoleamine 2,3‐dioxygenase (IDO)‐1 and IDO‐2 activity and severe course of COVID‐19 |
title | Indoleamine 2,3‐dioxygenase (IDO)‐1 and IDO‐2 activity and severe course of COVID‐19 |
title_full | Indoleamine 2,3‐dioxygenase (IDO)‐1 and IDO‐2 activity and severe course of COVID‐19 |
title_fullStr | Indoleamine 2,3‐dioxygenase (IDO)‐1 and IDO‐2 activity and severe course of COVID‐19 |
title_full_unstemmed | Indoleamine 2,3‐dioxygenase (IDO)‐1 and IDO‐2 activity and severe course of COVID‐19 |
title_short | Indoleamine 2,3‐dioxygenase (IDO)‐1 and IDO‐2 activity and severe course of COVID‐19 |
title_sort | indoleamine 2,3‐dioxygenase (ido)‐1 and ido‐2 activity and severe course of covid‐19 |
topic | Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897979/ https://www.ncbi.nlm.nih.gov/pubmed/34859884 http://dx.doi.org/10.1002/path.5842 |
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