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http://hdl.handle.net/123456789/713
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DC Field | Value | Language |
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dc.contributor.author | Surolia, Avadhesha | - |
dc.date.accessioned | 2016-03-31T05:43:11Z | - |
dc.date.available | 2016-03-31T05:43:11Z | - |
dc.date.issued | 2015-02 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/713 | - |
dc.description.abstract | Protein therapeutics targeting inflammatory mediators have shown great promise for the treatment of autoimmunities such as rheumatoid arthritis (RA). However, a significant challenge in this area has been their low in vivo stability and consequently their severely compromised therapeutic efficacy. One such therapeutic molecule IL-1 receptor antagonist (IL-1ra), used in the treatment of rheumatoid arthritis, has displayed only modest efficacy in human clinical trials owing to its short biological half-life. Herein, we report a novel approach to conglomerate individual protein entities into a drug depot by incorporation of an amyloidogenic motif Lys-Phe-Phe-Glu (KFFE) thereby dramatically improving their systemic persistence and in turn their therapeutic efficacy in a mice model of autoimmune arthritis. | en_US |
dc.publisher | Elsevier Ltd | en_US |
dc.title | Novel multimeric IL-1 receptor antagonist for the treatment of rheumatoid arthritis | en_US |
dc.contributor.coauthor | Pasi, Shweta | - |
dc.contributor.coauthor | Kant, Ravi | - |
dc.contributor.coauthor | Gupta, Sarika | - |
dc.keyword | IL-1 receptor antagonist, Multimeric, Rheumatoid arthritis, Anakinra | en_US |
dc.journal | Biomaterials | en_US |
dc.volumeno | 42 | en_US |
dc.pages | 121-133 | en_US |
Appears in Collections: | Molecular Sciences, Publications |
Files in This Item:
File | Description | Size | Format | |
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1-s2.0-S0142961214012186-main.pdf | Research article (access limited) | 2.72 MB | Adobe PDF | View/Open Request a copy |
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