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Impact of immunization against OxLDL on the pulmonary response to cigarette smoke exposure in mice
BACKGROUND: Cigarette smoke exposure can affect pulmonary lipid homeostasis and cause a progressive increase in pulmonary antibodies against oxidized low-density lipoproteins (OxLDL). Similarly, increased anti-OxLDL antibodies are observed in atherosclerosis, a pathology also tightly associated with...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029023/ https://www.ncbi.nlm.nih.gov/pubmed/29970083 http://dx.doi.org/10.1186/s12931-018-0833-9 |
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author | Talbot, Maude Hamel-Auger, Mélanie Beaulieu, Marie-Josée Gazzola, Morgan Lechasseur, Ariane Aubin, Sophie Paré, Marie-Ève Marsolais, David Bossé, Ynuk Morissette, Mathieu C. |
author_facet | Talbot, Maude Hamel-Auger, Mélanie Beaulieu, Marie-Josée Gazzola, Morgan Lechasseur, Ariane Aubin, Sophie Paré, Marie-Ève Marsolais, David Bossé, Ynuk Morissette, Mathieu C. |
author_sort | Talbot, Maude |
collection | PubMed |
description | BACKGROUND: Cigarette smoke exposure can affect pulmonary lipid homeostasis and cause a progressive increase in pulmonary antibodies against oxidized low-density lipoproteins (OxLDL). Similarly, increased anti-OxLDL antibodies are observed in atherosclerosis, a pathology also tightly associated with smoking and lipid homeostasis disruption. Several immunization strategies against oxidized lipid species to help with their clearance have been shown to reduce the formation of atherosclerotic lesions. Since oxidized lipids are generated during cigarette smoke exposure, we investigated the impact of a prophylactic immunization protocol against OxLDL on the pulmonary effects of cigarette smoke exposure in mice. METHODS: Mice were immunized systemically with a mixture of human OxLDL (antigen source) and AddaVax (adjuvant) or PBS alone prior to the initiation of acute (2 week) or sub-chronic (8 weeks) cigarette smoke exposure protocols. Anti-OxLDL antibodies were measured in the bronchoalveolar lavage (BAL) fluid and serum by direct ELISA. Pulmonary impacts of cigarette smoke exposure and OxLDL immunization were assessed by measuring BAL inflammatory cells, lung functions, and changes in lung structure and gene levels of matrix/matrix-related genes. RESULTS: Immunization to OxLDL led to a marked increase in circulating and pulmonary antibodies against OxLDL that persisted during cigarette smoke exposure. OxLDL immunization did not exacerbate or reduce the inflammatory response following acute or sub-chronic exposure to cigarette smoke. OxLDL immunization alone had effects similar to cigarette smoke exposure on lung functions but OxLDL immunization and cigarette smoke exposure had no additive effects on these parameters. No obvious changes in lung histology, airspace or levels of matrix and matrix-related genes were caused by OxLDL immunization compared to vehicle treatment. CONCLUSIONS: Overall, this study shows for the first time that a prophylactic immunization protocol against OxLDL can potentially have detrimental effects lung functions, without having additive effects over cigarette smoke exposure. This work sheds light on a complex dynamic between anti-OxLDL antibodies and the pulmonary response to cigarette smoke exposure. |
format | Online Article Text |
id | pubmed-6029023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60290232018-07-09 Impact of immunization against OxLDL on the pulmonary response to cigarette smoke exposure in mice Talbot, Maude Hamel-Auger, Mélanie Beaulieu, Marie-Josée Gazzola, Morgan Lechasseur, Ariane Aubin, Sophie Paré, Marie-Ève Marsolais, David Bossé, Ynuk Morissette, Mathieu C. Respir Res Research BACKGROUND: Cigarette smoke exposure can affect pulmonary lipid homeostasis and cause a progressive increase in pulmonary antibodies against oxidized low-density lipoproteins (OxLDL). Similarly, increased anti-OxLDL antibodies are observed in atherosclerosis, a pathology also tightly associated with smoking and lipid homeostasis disruption. Several immunization strategies against oxidized lipid species to help with their clearance have been shown to reduce the formation of atherosclerotic lesions. Since oxidized lipids are generated during cigarette smoke exposure, we investigated the impact of a prophylactic immunization protocol against OxLDL on the pulmonary effects of cigarette smoke exposure in mice. METHODS: Mice were immunized systemically with a mixture of human OxLDL (antigen source) and AddaVax (adjuvant) or PBS alone prior to the initiation of acute (2 week) or sub-chronic (8 weeks) cigarette smoke exposure protocols. Anti-OxLDL antibodies were measured in the bronchoalveolar lavage (BAL) fluid and serum by direct ELISA. Pulmonary impacts of cigarette smoke exposure and OxLDL immunization were assessed by measuring BAL inflammatory cells, lung functions, and changes in lung structure and gene levels of matrix/matrix-related genes. RESULTS: Immunization to OxLDL led to a marked increase in circulating and pulmonary antibodies against OxLDL that persisted during cigarette smoke exposure. OxLDL immunization did not exacerbate or reduce the inflammatory response following acute or sub-chronic exposure to cigarette smoke. OxLDL immunization alone had effects similar to cigarette smoke exposure on lung functions but OxLDL immunization and cigarette smoke exposure had no additive effects on these parameters. No obvious changes in lung histology, airspace or levels of matrix and matrix-related genes were caused by OxLDL immunization compared to vehicle treatment. CONCLUSIONS: Overall, this study shows for the first time that a prophylactic immunization protocol against OxLDL can potentially have detrimental effects lung functions, without having additive effects over cigarette smoke exposure. This work sheds light on a complex dynamic between anti-OxLDL antibodies and the pulmonary response to cigarette smoke exposure. BioMed Central 2018-07-03 2018 /pmc/articles/PMC6029023/ /pubmed/29970083 http://dx.doi.org/10.1186/s12931-018-0833-9 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Talbot, Maude Hamel-Auger, Mélanie Beaulieu, Marie-Josée Gazzola, Morgan Lechasseur, Ariane Aubin, Sophie Paré, Marie-Ève Marsolais, David Bossé, Ynuk Morissette, Mathieu C. Impact of immunization against OxLDL on the pulmonary response to cigarette smoke exposure in mice |
title | Impact of immunization against OxLDL on the pulmonary response to cigarette smoke exposure in mice |
title_full | Impact of immunization against OxLDL on the pulmonary response to cigarette smoke exposure in mice |
title_fullStr | Impact of immunization against OxLDL on the pulmonary response to cigarette smoke exposure in mice |
title_full_unstemmed | Impact of immunization against OxLDL on the pulmonary response to cigarette smoke exposure in mice |
title_short | Impact of immunization against OxLDL on the pulmonary response to cigarette smoke exposure in mice |
title_sort | impact of immunization against oxldl on the pulmonary response to cigarette smoke exposure in mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029023/ https://www.ncbi.nlm.nih.gov/pubmed/29970083 http://dx.doi.org/10.1186/s12931-018-0833-9 |
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