Old and new therapeutics for Rheumatoid Arthritis: in vivo models and drug development
Abstract
Development of novel drugs for treatment of chronic inflammatory diseases is to a large extent dependent on the availability of good experimental in vivo models in order to perform preclinical tests of new drugs and for the identification of novel drug targets. Here, we review a number of existing rodent models for Rheumatoid Arthritis in the context of how these models have been utilized for developing established therapy in Rheumatoid Arthritis and, furthermore, the present use of animal models for studies of novel drug candidates. We have studied the literature in the field for the use of in vivo models during development of anti-rheumatic drugs; from Methotrexate to various antibody treatments, to novel drugs that are, or have recently been, in clinical trials. For novel drugs, we have explored websites for clinical trials. Although a single Rheumatoid Arthritis in vivo model cannot mirror the complexity of disease development, there exist a number of good animal models for Rheumatoid Arthritis, each defining some parts in disease development, which are useful for studies of drug response. We find that many of the established drugs were not tested in in vivo models before being used in the clinic, but rather animal models have been subsequently used to find mechanisms for efficacy. Finally, we report a number of novel drugs, tested in preclinical in vivo models, presently in clinical trials.
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B lymphocytes and autoantibodies are key in aspects of RA pathogenesis, and the clinical success of B cell targeted therapies further strengthens this.
“It has recently been acknowledged that B lymphocytes and autoantibodies are key in aspects of RA pathogenesis [48, 49] and the clinical success of B cell targeted therapies further strengthens this [6, 50].”
From The oncoprotein TBX3 is controlling severity in experimental arthritis (2019) · cites this paper as [6]
Cites
Divergent Pro- and Antiinflammatory Roles for IL-23 and IL-12 in Joint Autoimmune Inflammation
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The oncoprotein TBX3 is controlling severity in experimental arthritis
Sardar, S., Kerr, A., Vaartjes, D., Moltved, E. R., Karosiene, E., Gupta, R., & Andersson, Å. (2019) · Arthritis Research & Therapy · doi:10.1186/s13075-018-1797-3 · Cited by 13 · see citing works
“arthritis (CIA) is the most commonly used model [6].”
BackgroundSelf-citationSardar, S., Kanne, K., & Andersson, Å. (2018) · Archivum Immunologiae et Therapiae Experimentalis · doi:10.1007/s00005-018-0516-8 · Cited by 3 · see citing works
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- Authors
- Sardar, S., & Andersson, Å.
- Affiliations
- University of Copenhagen (DK)
- Corresponding author
- Andersson, Åsa
- Venue
- Immunopharmacology and Immunotoxicology
- Publisher
- Informa UK Limited
- Published
- 2016-01-02
- Volume
- 38
- Issue
- 1
- Pages
- 2-13
- ISSN
- 0892-3973 (ISSN-L)
- 1532-2513
- OpenAlex
- W2292944301
- Cited by
- 50
- References
- 4
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 2 · 2023: 4 · 2022: 9 · 2021: 3 · 2020: 4 · 2019: 9 · 2018: 5 · 2017: 6
- FWCI
- 1.05
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Immunopharmacology and Immunotoxicology (publishedVersion)
- PubMed (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- Topics
- Health Sciences › Medicine › Rheumatology › Rheumatoid Arthritis Research and Therapies
- Health Sciences › Medicine › Complementary and alternative medicine › Natural Compounds in Disease Treatment
- Life Sciences › Immunology and Microbiology › Immunology › Immunotoxicology and immune responses
- Keywords
- rheumatoid arthritis, rodent models, methotrexate, novel drug candidates, clinical trials, preclinical drug testing, chronic inflammatory diseases
- MeSH terms
- Animals, Arthritis, Experimental, Arthritis, Rheumatoid, Humans, Drug Design, Antirheumatic Agents
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