Biological drugs targeting the immune response in the therapy of psoriasis

Saveria Pastore1, Emanuela Gubinelli2, Luca Leoni2, Desanka Raskovic2, Liudmila Korkina11Laboratory of Tissue Engineering and Cutaneous Physiopathology; 2Second Dermatology Unit, Istituto Dermopatico dell’Immacolata, IRCCS, Roma, ItalyAbstract: Chronic plaque psoriasis affects more tha...

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Autores principales: Saveria Pastore, Emanuela Gubinelli, Luca Leoni, Desanka Raskovic, Liudmila Korkina
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Publicado: Dove Medical Press 2008
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Acceso en línea:https://doaj.org/article/9de126c3b1d942e69085e0b6d7c9d1c0
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spelling oai:doaj.org-article:9de126c3b1d942e69085e0b6d7c9d1c02021-12-02T04:13:34ZBiological drugs targeting the immune response in the therapy of psoriasis1177-54751177-5491https://doaj.org/article/9de126c3b1d942e69085e0b6d7c9d1c02008-08-01T00:00:00Zhttp://www.dovepress.com/biological-drugs-targeting-the-immune-response-in-the-therapy-of-psori-a1950https://doaj.org/toc/1177-5475https://doaj.org/toc/1177-5491Saveria Pastore1, Emanuela Gubinelli2, Luca Leoni2, Desanka Raskovic2, Liudmila Korkina11Laboratory of Tissue Engineering and Cutaneous Physiopathology; 2Second Dermatology Unit, Istituto Dermopatico dell’Immacolata, IRCCS, Roma, ItalyAbstract: Chronic plaque psoriasis affects more than 2% of world population, has a chronic recurrent behavior, gives a heavy burden to the patients’ quality of life, and hence remains a huge medical and social problem. The clinical results of conventional therapies of psoriasis are not satisfactory. According to the current knowledge of the molecular and cellular basis of psoriasis, it is defined as an immune-mediated chronic inflammatory and hyperproliferative skin disease. A new generation of biological drugs, targeting molecules and cells involved into perturbed pro-inflammatory immune response in the psoriatic skin and joints, has been recently designed and applied clinically. These biological agents are bioengineered proteins such as chimeric and humanized antibodies and fusion proteins. In particular, they comprise the antitumor necrosis factor-α agents etanercept, infliximab, and adalimumab, with clinical efficacy in both moderate-severe psoriasis and psoriatic arthritis, and the anti-CD11a efalizumab with selective therapeutic action exclusively in the skin. Here, we overview recent findings on the molecular pathways relevant to the inflammatory response in psoriasis and present our clinical experience with the drugs currently employed in the dermatologic manifestations, namely etanercept, infliximab, and efalizumab. The growing body of clinical data on the efficacy and safety of antipsoriasis biological drugs is reviewed as well. Particular focus is given to long-term safety concerns and feasibility of combined therapeutic protocols to ameliorate clinical results.Keywords: psoriasis, immune-mediated inflammation, etanercept, infliximab, efalizumab Saveria PastoreEmanuela GubinelliLuca LeoniDesanka RaskovicLiudmila KorkinaDove Medical PressarticleMedicine (General)R5-920ENBiologics: Targets & Therapy, Vol 2008, Iss Issue 4, Pp 687-697 (2008)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
Saveria Pastore
Emanuela Gubinelli
Luca Leoni
Desanka Raskovic
Liudmila Korkina
Biological drugs targeting the immune response in the therapy of psoriasis
description Saveria Pastore1, Emanuela Gubinelli2, Luca Leoni2, Desanka Raskovic2, Liudmila Korkina11Laboratory of Tissue Engineering and Cutaneous Physiopathology; 2Second Dermatology Unit, Istituto Dermopatico dell’Immacolata, IRCCS, Roma, ItalyAbstract: Chronic plaque psoriasis affects more than 2% of world population, has a chronic recurrent behavior, gives a heavy burden to the patients’ quality of life, and hence remains a huge medical and social problem. The clinical results of conventional therapies of psoriasis are not satisfactory. According to the current knowledge of the molecular and cellular basis of psoriasis, it is defined as an immune-mediated chronic inflammatory and hyperproliferative skin disease. A new generation of biological drugs, targeting molecules and cells involved into perturbed pro-inflammatory immune response in the psoriatic skin and joints, has been recently designed and applied clinically. These biological agents are bioengineered proteins such as chimeric and humanized antibodies and fusion proteins. In particular, they comprise the antitumor necrosis factor-α agents etanercept, infliximab, and adalimumab, with clinical efficacy in both moderate-severe psoriasis and psoriatic arthritis, and the anti-CD11a efalizumab with selective therapeutic action exclusively in the skin. Here, we overview recent findings on the molecular pathways relevant to the inflammatory response in psoriasis and present our clinical experience with the drugs currently employed in the dermatologic manifestations, namely etanercept, infliximab, and efalizumab. The growing body of clinical data on the efficacy and safety of antipsoriasis biological drugs is reviewed as well. Particular focus is given to long-term safety concerns and feasibility of combined therapeutic protocols to ameliorate clinical results.Keywords: psoriasis, immune-mediated inflammation, etanercept, infliximab, efalizumab
format article
author Saveria Pastore
Emanuela Gubinelli
Luca Leoni
Desanka Raskovic
Liudmila Korkina
author_facet Saveria Pastore
Emanuela Gubinelli
Luca Leoni
Desanka Raskovic
Liudmila Korkina
author_sort Saveria Pastore
title Biological drugs targeting the immune response in the therapy of psoriasis
title_short Biological drugs targeting the immune response in the therapy of psoriasis
title_full Biological drugs targeting the immune response in the therapy of psoriasis
title_fullStr Biological drugs targeting the immune response in the therapy of psoriasis
title_full_unstemmed Biological drugs targeting the immune response in the therapy of psoriasis
title_sort biological drugs targeting the immune response in the therapy of psoriasis
publisher Dove Medical Press
publishDate 2008
url https://doaj.org/article/9de126c3b1d942e69085e0b6d7c9d1c0
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AT lucaleoni biologicaldrugstargetingtheimmuneresponseinthetherapyofpsoriasis
AT desankaraskovic biologicaldrugstargetingtheimmuneresponseinthetherapyofpsoriasis
AT liudmilakorkina biologicaldrugstargetingtheimmuneresponseinthetherapyofpsoriasis
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