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Impact of immunization against OxLDL on the pulmonary response to cigarette smoke exposure in mice. | LitMetric

AI Article Synopsis

  • Cigarette smoke exposure disrupts lipid balance in the lungs and increases antibodies against oxidized low-density lipoproteins (OxLDL), a condition linked to atherosclerosis, prompting research on immunization against OxLDL to mitigate these effects in mice.
  • Mice were treated with OxLDL immunization before being exposed to cigarette smoke, and their lung health was monitored by measuring immune responses, lung function, and tissue structure, but no significant improvements or worsening were observed.
  • The study concluded that while OxLDL immunization increased antibodies, it did not affect inflammation or lung damage caused by cigarette smoke exposure, suggesting that simply boosting the immune response to OxLDL may not combat lung

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029023PMC
http://dx.doi.org/10.1186/s12931-018-0833-9DOI Listing

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