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First Recombinant High-Density Lipoprotein Particles Administration in a Severe ICU COVID-19 Patient, a Multi-Omics Exploratory Investigation
High-density lipoproteins (HDLs) have multiple endothelioprotective properties. During SARS-CoV-2 infection, HDL-cholesterol (HDL-C) concentration is markedly reduced, and studies have described severe impairment of the functionality of HDL particles. Here, we report a multi-omic investigation of th...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9029957/ https://www.ncbi.nlm.nih.gov/pubmed/35453504 http://dx.doi.org/10.3390/biomedicines10040754 |
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author | Tanaka, Sébastien Begue, Floran Veeren, Bryan Tran-Dinh, Alexy Robert, Tiphaine Tashk, Parvine Lortat-Jacob, Brice Faille, Dorothée de Chaisemartin, Luc Zappella, Nathalie Atchade, Enora Kramer, Laura Montravers, Philippe Meilhac, Olivier |
author_facet | Tanaka, Sébastien Begue, Floran Veeren, Bryan Tran-Dinh, Alexy Robert, Tiphaine Tashk, Parvine Lortat-Jacob, Brice Faille, Dorothée de Chaisemartin, Luc Zappella, Nathalie Atchade, Enora Kramer, Laura Montravers, Philippe Meilhac, Olivier |
author_sort | Tanaka, Sébastien |
collection | PubMed |
description | High-density lipoproteins (HDLs) have multiple endothelioprotective properties. During SARS-CoV-2 infection, HDL-cholesterol (HDL-C) concentration is markedly reduced, and studies have described severe impairment of the functionality of HDL particles. Here, we report a multi-omic investigation of the first administration of recombinant HDL (rHDL) particles in a severe COVID-19 patient in an intensive care unit. Plasma ApoA1 increased and HDL-C decreased after each recombinant HDL injection, suggesting that these particles were functional in terms of reverse cholesterol transport. The proportion of large HDL particles also increased after injection of recombinant HDL. Shotgun proteomics performed on HDLs isolated by ultracentrifugation indicated that ApoA1 was more abundant after injections whereas most of the pro-inflammatory proteins identified were less abundant. Assessment of Serum amyloid A-1, inflammatory markers, and cytokines showed a significant decrease for most of them during recombinant HDL infusion. Our results suggest that recombinant HDL infusion is feasible and a potential therapeutic strategy to be explored in COVID-19 patients. |
format | Online Article Text |
id | pubmed-9029957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90299572022-04-23 First Recombinant High-Density Lipoprotein Particles Administration in a Severe ICU COVID-19 Patient, a Multi-Omics Exploratory Investigation Tanaka, Sébastien Begue, Floran Veeren, Bryan Tran-Dinh, Alexy Robert, Tiphaine Tashk, Parvine Lortat-Jacob, Brice Faille, Dorothée de Chaisemartin, Luc Zappella, Nathalie Atchade, Enora Kramer, Laura Montravers, Philippe Meilhac, Olivier Biomedicines Case Report High-density lipoproteins (HDLs) have multiple endothelioprotective properties. During SARS-CoV-2 infection, HDL-cholesterol (HDL-C) concentration is markedly reduced, and studies have described severe impairment of the functionality of HDL particles. Here, we report a multi-omic investigation of the first administration of recombinant HDL (rHDL) particles in a severe COVID-19 patient in an intensive care unit. Plasma ApoA1 increased and HDL-C decreased after each recombinant HDL injection, suggesting that these particles were functional in terms of reverse cholesterol transport. The proportion of large HDL particles also increased after injection of recombinant HDL. Shotgun proteomics performed on HDLs isolated by ultracentrifugation indicated that ApoA1 was more abundant after injections whereas most of the pro-inflammatory proteins identified were less abundant. Assessment of Serum amyloid A-1, inflammatory markers, and cytokines showed a significant decrease for most of them during recombinant HDL infusion. Our results suggest that recombinant HDL infusion is feasible and a potential therapeutic strategy to be explored in COVID-19 patients. MDPI 2022-03-23 /pmc/articles/PMC9029957/ /pubmed/35453504 http://dx.doi.org/10.3390/biomedicines10040754 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 | Case Report Tanaka, Sébastien Begue, Floran Veeren, Bryan Tran-Dinh, Alexy Robert, Tiphaine Tashk, Parvine Lortat-Jacob, Brice Faille, Dorothée de Chaisemartin, Luc Zappella, Nathalie Atchade, Enora Kramer, Laura Montravers, Philippe Meilhac, Olivier First Recombinant High-Density Lipoprotein Particles Administration in a Severe ICU COVID-19 Patient, a Multi-Omics Exploratory Investigation |
title | First Recombinant High-Density Lipoprotein Particles Administration in a Severe ICU COVID-19 Patient, a Multi-Omics Exploratory Investigation |
title_full | First Recombinant High-Density Lipoprotein Particles Administration in a Severe ICU COVID-19 Patient, a Multi-Omics Exploratory Investigation |
title_fullStr | First Recombinant High-Density Lipoprotein Particles Administration in a Severe ICU COVID-19 Patient, a Multi-Omics Exploratory Investigation |
title_full_unstemmed | First Recombinant High-Density Lipoprotein Particles Administration in a Severe ICU COVID-19 Patient, a Multi-Omics Exploratory Investigation |
title_short | First Recombinant High-Density Lipoprotein Particles Administration in a Severe ICU COVID-19 Patient, a Multi-Omics Exploratory Investigation |
title_sort | first recombinant high-density lipoprotein particles administration in a severe icu covid-19 patient, a multi-omics exploratory investigation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9029957/ https://www.ncbi.nlm.nih.gov/pubmed/35453504 http://dx.doi.org/10.3390/biomedicines10040754 |
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