Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/713
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dc.contributor.authorSurolia, Avadhesha-
dc.date.accessioned2016-03-31T05:43:11Z-
dc.date.available2016-03-31T05:43:11Z-
dc.date.issued2015-02-
dc.identifier.urihttp://hdl.handle.net/123456789/713-
dc.description.abstractProtein 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.publisherElsevier Ltden_US
dc.titleNovel multimeric IL-1 receptor antagonist for the treatment of rheumatoid arthritisen_US
dc.contributor.coauthorPasi, Shweta-
dc.contributor.coauthorKant, Ravi-
dc.contributor.coauthorGupta, Sarika-
dc.keywordIL-1 receptor antagonist, Multimeric, Rheumatoid arthritis, Anakinraen_US
dc.journalBiomaterialsen_US
dc.volumeno42en_US
dc.pages121-133en_US
Appears in Collections:Molecular Sciences, Publications

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