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Rodent Preclinical Models for Developing Novel Antiarthritic Molecules: Comparative Biology and Preferred Methods for Evaluating Efficacy

Rodent models of immune-mediated arthritis (RMIA) are the conventional approach to evaluating mechanisms of inflammatory joint disease and the comparative efficacy of antiarthritic agents. Rat adjuvant-induced (AIA), collagen-induced (CIA), and streptococcal cell wall-induced (SCW) arthritides are p...

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Autores principales: Bolon, Brad, Stolina, Marina, King, Caroline, Middleton, Scot, Gasser, Jill, Zack, Debra, Feige, Ulrich
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022224/
https://www.ncbi.nlm.nih.gov/pubmed/21253435
http://dx.doi.org/10.1155/2011/569068
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author Bolon, Brad
Stolina, Marina
King, Caroline
Middleton, Scot
Gasser, Jill
Zack, Debra
Feige, Ulrich
author_facet Bolon, Brad
Stolina, Marina
King, Caroline
Middleton, Scot
Gasser, Jill
Zack, Debra
Feige, Ulrich
author_sort Bolon, Brad
collection PubMed
description Rodent models of immune-mediated arthritis (RMIA) are the conventional approach to evaluating mechanisms of inflammatory joint disease and the comparative efficacy of antiarthritic agents. Rat adjuvant-induced (AIA), collagen-induced (CIA), and streptococcal cell wall-induced (SCW) arthritides are preferred models of the joint pathology that occurs in human rheumatoid arthritis (RA). Lesions of AIA are most severe and consistent; structural and immunological changes of CIA best resemble RA. Lesion extent and severity in RMIA depends on experimental methodology (inciting agent, adjuvant, etc.) and individual physiologic parameters (age, genetics, hormonal status, etc.). The effectiveness of antiarthritic molecules varies with the agent, therapeutic regimen, and choice of RMIA. All RMIA are driven by overactivity of proinflammatory pathways, but the dominant molecules differ among the models. Hence, as with the human clinical experience, the efficacy of various antiarthritic molecules differs among RMIA, especially when the agent is a specific cytokine inhibitor.
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spelling pubmed-30222242011-01-20 Rodent Preclinical Models for Developing Novel Antiarthritic Molecules: Comparative Biology and Preferred Methods for Evaluating Efficacy Bolon, Brad Stolina, Marina King, Caroline Middleton, Scot Gasser, Jill Zack, Debra Feige, Ulrich J Biomed Biotechnol Review Article Rodent models of immune-mediated arthritis (RMIA) are the conventional approach to evaluating mechanisms of inflammatory joint disease and the comparative efficacy of antiarthritic agents. Rat adjuvant-induced (AIA), collagen-induced (CIA), and streptococcal cell wall-induced (SCW) arthritides are preferred models of the joint pathology that occurs in human rheumatoid arthritis (RA). Lesions of AIA are most severe and consistent; structural and immunological changes of CIA best resemble RA. Lesion extent and severity in RMIA depends on experimental methodology (inciting agent, adjuvant, etc.) and individual physiologic parameters (age, genetics, hormonal status, etc.). The effectiveness of antiarthritic molecules varies with the agent, therapeutic regimen, and choice of RMIA. All RMIA are driven by overactivity of proinflammatory pathways, but the dominant molecules differ among the models. Hence, as with the human clinical experience, the efficacy of various antiarthritic molecules differs among RMIA, especially when the agent is a specific cytokine inhibitor. Hindawi Publishing Corporation 2011 2010-12-28 /pmc/articles/PMC3022224/ /pubmed/21253435 http://dx.doi.org/10.1155/2011/569068 Text en Copyright © 2011 Brad Bolon et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Bolon, Brad
Stolina, Marina
King, Caroline
Middleton, Scot
Gasser, Jill
Zack, Debra
Feige, Ulrich
Rodent Preclinical Models for Developing Novel Antiarthritic Molecules: Comparative Biology and Preferred Methods for Evaluating Efficacy
title Rodent Preclinical Models for Developing Novel Antiarthritic Molecules: Comparative Biology and Preferred Methods for Evaluating Efficacy
title_full Rodent Preclinical Models for Developing Novel Antiarthritic Molecules: Comparative Biology and Preferred Methods for Evaluating Efficacy
title_fullStr Rodent Preclinical Models for Developing Novel Antiarthritic Molecules: Comparative Biology and Preferred Methods for Evaluating Efficacy
title_full_unstemmed Rodent Preclinical Models for Developing Novel Antiarthritic Molecules: Comparative Biology and Preferred Methods for Evaluating Efficacy
title_short Rodent Preclinical Models for Developing Novel Antiarthritic Molecules: Comparative Biology and Preferred Methods for Evaluating Efficacy
title_sort rodent preclinical models for developing novel antiarthritic molecules: comparative biology and preferred methods for evaluating efficacy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022224/
https://www.ncbi.nlm.nih.gov/pubmed/21253435
http://dx.doi.org/10.1155/2011/569068
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