Loading…

Animal models of psoriasis—highlights and drawbacks

Research into the pathophysiology of psoriasis remains challenging, because this disease does not occur naturally in laboratory animals. However, specific aspects of its complex immune-pathology can be illuminated through transgenic, knockout, xenotransplantation, immunological reconstitution, drug-...

Full description

Saved in:
Bibliographic Details
Published in:Journal of allergy and clinical immunology 2021-02, Vol.147 (2), p.439-455
Main Authors: Schön, Michael P., Manzke, Veit, Erpenbeck, Luise
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c400t-172f663b5a2b7ff6faca79831325dfada6dbae0a45627e626716c0be9f00f9c53
cites cdi_FETCH-LOGICAL-c400t-172f663b5a2b7ff6faca79831325dfada6dbae0a45627e626716c0be9f00f9c53
container_end_page 455
container_issue 2
container_start_page 439
container_title Journal of allergy and clinical immunology
container_volume 147
creator Schön, Michael P.
Manzke, Veit
Erpenbeck, Luise
description Research into the pathophysiology of psoriasis remains challenging, because this disease does not occur naturally in laboratory animals. However, specific aspects of its complex immune-pathology can be illuminated through transgenic, knockout, xenotransplantation, immunological reconstitution, drug-induced, or spontaneous mutation models in rodents. Although some of these approaches have already been pursued for more than 5 decades and even more models have been described in recent times, they have surprisingly not yet been systematically validated. As a consequence, researchers regularly examine specific aspects that only partially reflect the complex overall picture of the human disease. Nonetheless, animal models are of great utility to investigate inflammatory mediators, the communication between cells of the innate and the adaptive immune systems, the role of resident cells as well as new therapies. Of note, various manipulations in experimental animals resulted in rather similar phenotypes. These were called “psoriasiform”, “psoriasis-like” or even “psoriasis” usually on the basis of some similarities with the human disorder. Xenotransplantation of human skin onto immunocompromised animals can overcome this limitation only in part. In this review, we elucidate approaches for the generation of animal models of psoriasis and assess their strengths and limitations with a certain focus on more recently developed models.
doi_str_mv 10.1016/j.jaci.2020.04.034
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2415297806</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0091674920306308</els_id><sourcerecordid>2415297806</sourcerecordid><originalsourceid>FETCH-LOGICAL-c400t-172f663b5a2b7ff6faca79831325dfada6dbae0a45627e626716c0be9f00f9c53</originalsourceid><addsrcrecordid>eNp9kEtOwzAQhi0EoqVwARYoSzYJYyexY4lNVfGSkNjA2nL8oA55FDsFseMQnJCT4KqFJYvRaKRv_tF8CJ1iyDBgetFkjVQuI0AggyKDvNhDUwycpbQi5T6aAnCcUlbwCToKoYE45xU_RJOclDRyeIrKee862SbdoE0bksEmqzB4J4ML359fS_e8bGONIZG9TrSX77VUL-EYHVjZBnOy6zP0dH31uLhN7x9u7hbz-1QVAGOKGbGU5nUpSc2spVYqyXiV43hfW6kl1bU0IIuSEmYooQxTBbXhFsByVeYzdL7NXfnhdW3CKDoXlGlb2ZthHQQpcEk4q4BGlGxR5YcQvLFi5eNn_kNgEBtdohEbXWKjS0Ahoq64dLbLX9ed0X8rv34icLkFohzz5owXQTnTK6OdN2oUenD_5f8Agut8GQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2415297806</pqid></control><display><type>article</type><title>Animal models of psoriasis—highlights and drawbacks</title><source>ScienceDirect Freedom Collection 2022-2024</source><creator>Schön, Michael P. ; Manzke, Veit ; Erpenbeck, Luise</creator><creatorcontrib>Schön, Michael P. ; Manzke, Veit ; Erpenbeck, Luise</creatorcontrib><description>Research into the pathophysiology of psoriasis remains challenging, because this disease does not occur naturally in laboratory animals. However, specific aspects of its complex immune-pathology can be illuminated through transgenic, knockout, xenotransplantation, immunological reconstitution, drug-induced, or spontaneous mutation models in rodents. Although some of these approaches have already been pursued for more than 5 decades and even more models have been described in recent times, they have surprisingly not yet been systematically validated. As a consequence, researchers regularly examine specific aspects that only partially reflect the complex overall picture of the human disease. Nonetheless, animal models are of great utility to investigate inflammatory mediators, the communication between cells of the innate and the adaptive immune systems, the role of resident cells as well as new therapies. Of note, various manipulations in experimental animals resulted in rather similar phenotypes. These were called “psoriasiform”, “psoriasis-like” or even “psoriasis” usually on the basis of some similarities with the human disorder. Xenotransplantation of human skin onto immunocompromised animals can overcome this limitation only in part. In this review, we elucidate approaches for the generation of animal models of psoriasis and assess their strengths and limitations with a certain focus on more recently developed models.</description><identifier>ISSN: 0091-6749</identifier><identifier>EISSN: 1097-6825</identifier><identifier>DOI: 10.1016/j.jaci.2020.04.034</identifier><identifier>PMID: 32560971</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>adoptive transfer ; animal model ; chronic inflammation ; dermatology ; drug testing ; epidermis ; hyperproliferation ; imiquimod ; preclinical ; preclinical therapeutic study ; Psoriasis ; skin immunity ; skin inflammation ; transgenic ; xenotransplantation</subject><ispartof>Journal of allergy and clinical immunology, 2021-02, Vol.147 (2), p.439-455</ispartof><rights>2020 The Authors</rights><rights>Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-172f663b5a2b7ff6faca79831325dfada6dbae0a45627e626716c0be9f00f9c53</citedby><cites>FETCH-LOGICAL-c400t-172f663b5a2b7ff6faca79831325dfada6dbae0a45627e626716c0be9f00f9c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,786,790,27957,27958</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32560971$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schön, Michael P.</creatorcontrib><creatorcontrib>Manzke, Veit</creatorcontrib><creatorcontrib>Erpenbeck, Luise</creatorcontrib><title>Animal models of psoriasis—highlights and drawbacks</title><title>Journal of allergy and clinical immunology</title><addtitle>J Allergy Clin Immunol</addtitle><description>Research into the pathophysiology of psoriasis remains challenging, because this disease does not occur naturally in laboratory animals. However, specific aspects of its complex immune-pathology can be illuminated through transgenic, knockout, xenotransplantation, immunological reconstitution, drug-induced, or spontaneous mutation models in rodents. Although some of these approaches have already been pursued for more than 5 decades and even more models have been described in recent times, they have surprisingly not yet been systematically validated. As a consequence, researchers regularly examine specific aspects that only partially reflect the complex overall picture of the human disease. Nonetheless, animal models are of great utility to investigate inflammatory mediators, the communication between cells of the innate and the adaptive immune systems, the role of resident cells as well as new therapies. Of note, various manipulations in experimental animals resulted in rather similar phenotypes. These were called “psoriasiform”, “psoriasis-like” or even “psoriasis” usually on the basis of some similarities with the human disorder. Xenotransplantation of human skin onto immunocompromised animals can overcome this limitation only in part. In this review, we elucidate approaches for the generation of animal models of psoriasis and assess their strengths and limitations with a certain focus on more recently developed models.</description><subject>adoptive transfer</subject><subject>animal model</subject><subject>chronic inflammation</subject><subject>dermatology</subject><subject>drug testing</subject><subject>epidermis</subject><subject>hyperproliferation</subject><subject>imiquimod</subject><subject>preclinical</subject><subject>preclinical therapeutic study</subject><subject>Psoriasis</subject><subject>skin immunity</subject><subject>skin inflammation</subject><subject>transgenic</subject><subject>xenotransplantation</subject><issn>0091-6749</issn><issn>1097-6825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kEtOwzAQhi0EoqVwARYoSzYJYyexY4lNVfGSkNjA2nL8oA55FDsFseMQnJCT4KqFJYvRaKRv_tF8CJ1iyDBgetFkjVQuI0AggyKDvNhDUwycpbQi5T6aAnCcUlbwCToKoYE45xU_RJOclDRyeIrKee862SbdoE0bksEmqzB4J4ML359fS_e8bGONIZG9TrSX77VUL-EYHVjZBnOy6zP0dH31uLhN7x9u7hbz-1QVAGOKGbGU5nUpSc2spVYqyXiV43hfW6kl1bU0IIuSEmYooQxTBbXhFsByVeYzdL7NXfnhdW3CKDoXlGlb2ZthHQQpcEk4q4BGlGxR5YcQvLFi5eNn_kNgEBtdohEbXWKjS0Ahoq64dLbLX9ed0X8rv34icLkFohzz5owXQTnTK6OdN2oUenD_5f8Agut8GQ</recordid><startdate>202102</startdate><enddate>202102</enddate><creator>Schön, Michael P.</creator><creator>Manzke, Veit</creator><creator>Erpenbeck, Luise</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202102</creationdate><title>Animal models of psoriasis—highlights and drawbacks</title><author>Schön, Michael P. ; Manzke, Veit ; Erpenbeck, Luise</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-172f663b5a2b7ff6faca79831325dfada6dbae0a45627e626716c0be9f00f9c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>adoptive transfer</topic><topic>animal model</topic><topic>chronic inflammation</topic><topic>dermatology</topic><topic>drug testing</topic><topic>epidermis</topic><topic>hyperproliferation</topic><topic>imiquimod</topic><topic>preclinical</topic><topic>preclinical therapeutic study</topic><topic>Psoriasis</topic><topic>skin immunity</topic><topic>skin inflammation</topic><topic>transgenic</topic><topic>xenotransplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schön, Michael P.</creatorcontrib><creatorcontrib>Manzke, Veit</creatorcontrib><creatorcontrib>Erpenbeck, Luise</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of allergy and clinical immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schön, Michael P.</au><au>Manzke, Veit</au><au>Erpenbeck, Luise</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Animal models of psoriasis—highlights and drawbacks</atitle><jtitle>Journal of allergy and clinical immunology</jtitle><addtitle>J Allergy Clin Immunol</addtitle><date>2021-02</date><risdate>2021</risdate><volume>147</volume><issue>2</issue><spage>439</spage><epage>455</epage><pages>439-455</pages><issn>0091-6749</issn><eissn>1097-6825</eissn><notes>ObjectType-Article-2</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-3</notes><notes>content type line 23</notes><notes>ObjectType-Review-1</notes><abstract>Research into the pathophysiology of psoriasis remains challenging, because this disease does not occur naturally in laboratory animals. However, specific aspects of its complex immune-pathology can be illuminated through transgenic, knockout, xenotransplantation, immunological reconstitution, drug-induced, or spontaneous mutation models in rodents. Although some of these approaches have already been pursued for more than 5 decades and even more models have been described in recent times, they have surprisingly not yet been systematically validated. As a consequence, researchers regularly examine specific aspects that only partially reflect the complex overall picture of the human disease. Nonetheless, animal models are of great utility to investigate inflammatory mediators, the communication between cells of the innate and the adaptive immune systems, the role of resident cells as well as new therapies. Of note, various manipulations in experimental animals resulted in rather similar phenotypes. These were called “psoriasiform”, “psoriasis-like” or even “psoriasis” usually on the basis of some similarities with the human disorder. Xenotransplantation of human skin onto immunocompromised animals can overcome this limitation only in part. In this review, we elucidate approaches for the generation of animal models of psoriasis and assess their strengths and limitations with a certain focus on more recently developed models.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32560971</pmid><doi>10.1016/j.jaci.2020.04.034</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0091-6749
ispartof Journal of allergy and clinical immunology, 2021-02, Vol.147 (2), p.439-455
issn 0091-6749
1097-6825
language eng
recordid cdi_proquest_miscellaneous_2415297806
source ScienceDirect Freedom Collection 2022-2024
subjects adoptive transfer
animal model
chronic inflammation
dermatology
drug testing
epidermis
hyperproliferation
imiquimod
preclinical
preclinical therapeutic study
Psoriasis
skin immunity
skin inflammation
transgenic
xenotransplantation
title Animal models of psoriasis—highlights and drawbacks
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-09-23T05%3A16%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Animal%20models%20of%20psoriasis%E2%80%94highlights%20and%20drawbacks&rft.jtitle=Journal%20of%20allergy%20and%20clinical%20immunology&rft.au=Sch%C3%B6n,%20Michael%20P.&rft.date=2021-02&rft.volume=147&rft.issue=2&rft.spage=439&rft.epage=455&rft.pages=439-455&rft.issn=0091-6749&rft.eissn=1097-6825&rft_id=info:doi/10.1016/j.jaci.2020.04.034&rft_dat=%3Cproquest_cross%3E2415297806%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c400t-172f663b5a2b7ff6faca79831325dfada6dbae0a45627e626716c0be9f00f9c53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2415297806&rft_id=info:pmid/32560971&rfr_iscdi=true