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The novel small molecule drug Rabeximod is effective in reducing disease severity of mouse models of autoimmune disorders
Lund University, Lund, Sweden; Karolinska Institutet, Stockholm, Sweden; OxyPharma, Stockholm, Sweden.
Lund University, Lund, Sweden; Karolinska Institutet, Stockholm, Sweden; OxyPharma, Stockholm, Sweden.ORCID iD: 0000-0001-7790-8197
Lund University, Lund, Sweden; Karolinska Institutet, Stockholm, Sweden; OxyPharma, Stockholm, Sweden.
Lund University, Lund, Sweden; Karolinska Institutet, Stockholm, Sweden; OxyPharma, Stockholm, Sweden.
2009 (English)In: Annals of the Rheumatic Diseases, ISSN 0003-4967, E-ISSN 1468-2060, Vol. 68, no 1, p. 130-135Article in journal (Refereed) Published
Abstract [en]

OBJECTIVES: Autoimmune diseases such as rheumatoid arthritis (RA) and multiple sclerosis (MS) affect a relatively large portion of the population, leading to severe disability if left untreated. Even though pharmaceutics targeting the immune system have revolutionised the therapy of these diseases, there is still a need for novel, more effective therapeutic substances. One such substance is the new chemical entity 9-chloro-2,3 dimethyl-6-(N,N-dimthylamino-2-oxoethyl)-6H-indolo [2,3-b] quionoxaline, Rabeximod, currently being investigated for efficiency in treatment of human RA. In this study we aimed to evaluate Rabeximod as a treatment for autoimmune diseases, using animal models. METHODS: In the present investigation we have evaluated Rabeximod as a treatment for autoimmune diseases using mouse models of RA and MS, ie, collagen-induced arthritis, collagen antibody induced arthritis and experimental autoimmune encephalomyelitis. RESULTS: Rabeximod efficiently prevented arthritis and encephalomyelitis in mice. In addition, this effect correlated to the timepoint when cells migrate into the joints. CONCLUSIONS: We conclude that Rabeximod reduces disease severity in animal models of autoimmunity and should be considered as a new therapeutic substance for MS and RA.

Place, publisher, year, edition, pages
2009. Vol. 68, no 1, p. 130-135
Keywords [en]
Animals, Arthritis, Rheumatoid/drug therapy, Autoimmune Diseases/*drug therapy, Collagen, Cytokines/analysis, Disease Models, Animal, Immunosuppressive Agents/*therapeutic use, Indoles/*therapeutic use, Mice, Mice, Mutant Strains, Multiple Sclerosis/drug therapy, Quinoxalines/*therapeutic use, Rats, Reactive Oxygen Species/analysis/metabolism, Treatment Outcome
National Category
Rheumatology and Autoimmunity
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URN: urn:nbn:se:hh:diva-48849DOI: 10.1136/ard.2007.085241PubMedID: 18347009OAI: oai:DiVA.org:hh-48849DiVA, id: diva2:1719022
Available from: 2022-12-14 Created: 2022-12-14 Last updated: 2023-02-20Bibliographically approved

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Nandakumar, Kutty Selva

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