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dc.contributor.authorBadawi, Ahmed H.
dc.contributor.authorSiahaan, Teruna J.
dc.date.accessioned2017-06-07T19:30:42Z
dc.date.available2017-06-07T19:30:42Z
dc.date.issued2012-08
dc.identifier.citationBadawi, A. H., & Siahaan, T. J. (2012). Immune Modulating Peptides for the Treatment and Suppression of Multiple Sclerosis. Clinical Immunology (Orlando, Fla.), 144(2), 127–138. http://doi.org/10.1016/j.clim.2012.05.010en_US
dc.identifier.urihttp://hdl.handle.net/1808/24410
dc.description.abstractMultiple sclerosis (MS) is a neurodegenerative disease in which the immune system recognizes proteins of the myelin sheath as antigenic, thus initiating an inflammatory reaction in the central nervous system. This leads to demyelination of the axons, breakdown of the blood-brain barrier, and lesion formation. Current therapies for the treatment of MS are generally non-specific and weaken the global immune system, thus making the individual susceptible to opportunistic infections. Antigenic peptides and their derivatives are becoming more prevalent for investigation as therapeutic agents for MS because they possess immune-specific characteristics. In addition, other peptides that target vital components of the inflammatory immune response have also been developed. Therefore, the objectives of this review are to (a) summarize the immunological basis for the development of MS, (b) discuss specific and non-specific peptides tested in EAE and in humans, and (c) briefly address some problems and potential solutions with these novel therapies.en_US
dc.publisherElsevieren_US
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.subjectMultiple Sclerosisen_US
dc.subjectExperimental Autoimmune Encephalomyelitisen_US
dc.subjectPeptideen_US
dc.subjectAntigenen_US
dc.subjectBifunctional Peptide Inhibitoren_US
dc.titleImmune Modulating Peptides for the Treatment and Suppression of Multiple Sclerosisen_US
dc.typeArticleen_US
kusw.kuauthorBadawi, Ahmed H.
kusw.kuauthorSiahaan, Teruna J.
kusw.kudepartmentPharmaceutical Chemistryen_US
dc.identifier.doi10.1016/j.clim.2012.05.010en_US
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC3415220en_US
dc.rights.accessrightsopenAccess


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This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Except where otherwise noted, this item's license is described as: This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.