نمایش پرونده ساده آیتم

dc.contributor.authorJafari, R
dc.contributor.authorZolbanin, NM
dc.contributor.authorRafatpanah, H
dc.contributor.authorMajidi, J
dc.contributor.authorKazemi, T
dc.date.accessioned2018-08-26T07:21:53Z
dc.date.available2018-08-26T07:21:53Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/46189
dc.description.abstractFc-fusion proteins are composed of Fc region of IgG antibody (Hinge-CH2-CH3) and a desired linked protein. Fc region of Fc-fusion proteins can bind to neonatal Fc receptor (FcRn) thereby rescuing it from degradation. The first therapeutic Fc-fusion protein was introduced for the treatment of AIDS. The molecular designing is the first stage in production of Fc-fusion proteins. The amino acid residues in the Fc region and linked protein are very important in the bioactivity and affinity of the fusion proteins. Although, therapeutic monoclonal antibodies are the top selling biologics but the application of therapeutic Fc-fusion proteins in clinic is in progress and among these medications Etanercept is the most effective in therapy. At present, eleven Fc-fusion proteins have been approved by FDA. There are novel Fc-fusion proteins which are in pre-clinical and clinical development. In this article, we review the molecular and biological characteristics of Fc-fusion proteins and then further discuss the features of novel therapeutic Fc-fusion proteins.
dc.language.isoEnglish
dc.relation.ispartofCURRENT MEDICINAL CHEMISTRY
dc.subjectFc-fusion proteins
dc.subjectimmunotherapy
dc.subjectFcRn
dc.subjectantibody
dc.subjectFc region
dc.titleFc-fusion Proteins in Therapy: An Updated View
dc.typeReview
dc.citation.volume24
dc.citation.issue12
dc.citation.spage1228
dc.citation.epage1237
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.2174/0929867324666170113112759


فایلهای درون آیتم

فایلهاسایزفرمتنمایش

هیچ فایل مرتبطی وجود ندارد

این آیتم در مجموعه های زیر مشاهده می شود

نمایش پرونده ساده آیتم