Immunoproteasome inhibition attenuates experimental psoriasis
| dc.contributor.author | Del Rio Oliva, Marta | |
| dc.contributor.author | Mellett, Mark | |
| dc.contributor.author | Basler, Michael | |
| dc.date.accessioned | 2022-12-20T10:11:38Z | |
| dc.date.available | 2022-12-20T10:11:38Z | |
| dc.date.issued | 2022-12-14 | eng |
| dc.description.abstract | Introduction: Psoriasis is an autoimmune skin disease associated with multiple comorbidities. The immunoproteasome is a special form of the proteasome expressed in cells of hematopoietic origin. Methods: The therapeutic use of ONX 0914, a selective inhibitor of the immunoproteasome, was investigated in Card14ΔE138+/- mice, which spontaneously develop psoriasis-like symptoms, and in the imiquimod murine model. Results: In both models, treatment with ONX 0914 significantly reduced skin thickness, inflammation scores, and pathological lesions in the analyzed skin tissue. Furthermore, immunoproteasome inhibition normalized the expression of several pro-inflammatory genes in the ear and significantly reduced the inflammatory infiltrate, accompanied by a significant alteration in the αβ+ and γδ+ T cell subsets. Discussion: ONX 0914 ameliorated psoriasis-like symptoms in two different murine psoriasis models, which supports the use of immunoproteasome inhibitors as a therapeutic treatment in psoriasis. | eng |
| dc.description.version | published | de |
| dc.identifier.doi | 10.3389/fimmu.2022.1075615 | eng |
| dc.identifier.ppn | 1828118834 | |
| dc.identifier.uri | https://kops.uni-konstanz.de/handle/123456789/59567 | |
| dc.language.iso | eng | eng |
| dc.rights | Attribution 4.0 International | |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
| dc.subject | immunoproteasome inhibition, psoriasis, CARD14, imiquimod, ONX 0914 | eng |
| dc.subject.ddc | 570 | eng |
| dc.title | Immunoproteasome inhibition attenuates experimental psoriasis | eng |
| dc.type | JOURNAL_ARTICLE | de |
| dspace.entity.type | Publication | |
| kops.citation.bibtex | @article{DelRioOliva2022-12-14Immun-59567,
year={2022},
doi={10.3389/fimmu.2022.1075615},
title={Immunoproteasome inhibition attenuates experimental psoriasis},
volume={13},
journal={Frontiers in Immunology},
author={Del Rio Oliva, Marta and Mellett, Mark and Basler, Michael},
note={German Research Foundation (DFG) grant GR 1517/27-1 and SFB969 project C01
Corrigendum: https://doi.org/10.3389/fimmu.2023.1335691 Article Number: 1075615}
} | |
| kops.citation.iso690 | DEL RIO OLIVA, Marta, Mark MELLETT, Michael BASLER, 2022. Immunoproteasome inhibition attenuates experimental psoriasis. In: Frontiers in Immunology. Frontiers Media. 2022, 13, 1075615. eISSN 1664-3224. Available under: doi: 10.3389/fimmu.2022.1075615 | deu |
| kops.citation.iso690 | DEL RIO OLIVA, Marta, Mark MELLETT, Michael BASLER, 2022. Immunoproteasome inhibition attenuates experimental psoriasis. In: Frontiers in Immunology. Frontiers Media. 2022, 13, 1075615. eISSN 1664-3224. Available under: doi: 10.3389/fimmu.2022.1075615 | eng |
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<dcterms:abstract xml:lang="eng">Introduction: Psoriasis is an autoimmune skin disease associated with multiple comorbidities. The immunoproteasome is a special form of the proteasome expressed in cells of hematopoietic origin.<br /><br />Methods: The therapeutic use of ONX 0914, a selective inhibitor of the immunoproteasome, was investigated in Card14ΔE138<sup>+/-</sup> mice, which spontaneously develop psoriasis-like symptoms, and in the imiquimod murine model.<br /><br />Results: In both models, treatment with ONX 0914 significantly reduced skin thickness, inflammation scores, and pathological lesions in the analyzed skin tissue. Furthermore, immunoproteasome inhibition normalized the expression of several pro-inflammatory genes in the ear and significantly reduced the inflammatory infiltrate, accompanied by a significant alteration in the αβ<sup>+</sup> and γδ<sup>+</sup> T cell subsets.<br /><br />Discussion: ONX 0914 ameliorated psoriasis-like symptoms in two different murine psoriasis models, which supports the use of immunoproteasome inhibitors as a therapeutic treatment in psoriasis.</dcterms:abstract>
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| kops.description.comment | German Research Foundation (DFG) grant GR 1517/27-1 and SFB969 project C01 Corrigendum: https://doi.org/10.3389/fimmu.2023.1335691 | |
| kops.description.openAccess | openaccessgold | eng |
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| kops.identifier.nbn | urn:nbn:de:bsz:352-2-vuy7lolf6jkg8 | |
| kops.sourcefield | Frontiers in Immunology. Frontiers Media. 2022, <b>13</b>, 1075615. eISSN 1664-3224. Available under: doi: 10.3389/fimmu.2022.1075615 | deu |
| kops.sourcefield.plain | Frontiers in Immunology. Frontiers Media. 2022, 13, 1075615. eISSN 1664-3224. Available under: doi: 10.3389/fimmu.2022.1075615 | deu |
| kops.sourcefield.plain | Frontiers in Immunology. Frontiers Media. 2022, 13, 1075615. eISSN 1664-3224. Available under: doi: 10.3389/fimmu.2022.1075615 | eng |
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| source.bibliographicInfo.articleNumber | 1075615 | eng |
| source.bibliographicInfo.volume | 13 | eng |
| source.identifier.eissn | 1664-3224 | eng |
| source.periodicalTitle | Frontiers in Immunology | eng |
| source.publisher | Frontiers Media | eng |
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