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Old and New Biological Therapies for Psoriasis

Biological therapy became available for psoriasis with the introduction of alefacept at the beginning of this century. Up to then, systemic treatment options comprised small molecule drugs, targeting the immune system in a non-specific manner. The first biologics targeted T-cell activation and migra...

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Autores principales: Rønholt, Kirsten, Iversen, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713267/
https://www.ncbi.nlm.nih.gov/pubmed/29104241
http://dx.doi.org/10.3390/ijms18112297
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author Rønholt, Kirsten
Iversen, Lars
author_facet Rønholt, Kirsten
Iversen, Lars
author_sort Rønholt, Kirsten
collection PubMed
description Biological therapy became available for psoriasis with the introduction of alefacept at the beginning of this century. Up to then, systemic treatment options comprised small molecule drugs, targeting the immune system in a non-specific manner. The first biologics targeted T-cell activation and migration and served as an alternative to small molecules. However, significant improvement in outcome was first accomplished with the introduction of tumor necrosis factor-α inhibitors that were already approved for other inflammatory disorders, including rheumatic diseases. Along with the progress in understanding psoriasis pathogenesis, highly targeted and effective therapies have since developed with the perspective not only to improve but to clear psoriasis. These accomplishments enable future achievement of advanced goals to individualize treatment best suited for each patient. Mechanistic studies with patients treated with the new highly targeted biologics may guide us towards these goals. This review offers an overview of biologics developed for psoriasis and illustrate a historical progress in the treatment of this common chronic inflammatory skin condition.
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spelling pubmed-57132672017-12-07 Old and New Biological Therapies for Psoriasis Rønholt, Kirsten Iversen, Lars Int J Mol Sci Review Biological therapy became available for psoriasis with the introduction of alefacept at the beginning of this century. Up to then, systemic treatment options comprised small molecule drugs, targeting the immune system in a non-specific manner. The first biologics targeted T-cell activation and migration and served as an alternative to small molecules. However, significant improvement in outcome was first accomplished with the introduction of tumor necrosis factor-α inhibitors that were already approved for other inflammatory disorders, including rheumatic diseases. Along with the progress in understanding psoriasis pathogenesis, highly targeted and effective therapies have since developed with the perspective not only to improve but to clear psoriasis. These accomplishments enable future achievement of advanced goals to individualize treatment best suited for each patient. Mechanistic studies with patients treated with the new highly targeted biologics may guide us towards these goals. This review offers an overview of biologics developed for psoriasis and illustrate a historical progress in the treatment of this common chronic inflammatory skin condition. MDPI 2017-11-01 /pmc/articles/PMC5713267/ /pubmed/29104241 http://dx.doi.org/10.3390/ijms18112297 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Rønholt, Kirsten
Iversen, Lars
Old and New Biological Therapies for Psoriasis
title Old and New Biological Therapies for Psoriasis
title_full Old and New Biological Therapies for Psoriasis
title_fullStr Old and New Biological Therapies for Psoriasis
title_full_unstemmed Old and New Biological Therapies for Psoriasis
title_short Old and New Biological Therapies for Psoriasis
title_sort old and new biological therapies for psoriasis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713267/
https://www.ncbi.nlm.nih.gov/pubmed/29104241
http://dx.doi.org/10.3390/ijms18112297
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