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dc.contributor.authorMaleki, LA
dc.contributor.authorBaradaran, B
dc.contributor.authorMajidi, J
dc.contributor.authorMohammadian, M
dc.contributor.authorShahneh, FZ
dc.date.accessioned2018-08-26T08:55:58Z
dc.date.available2018-08-26T08:55:58Z
dc.date.issued2013
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54378
dc.description.abstractMonoclonal antibody therapy has become a critical component of clinical treatment procedure for a variety of indications. Therapeutic antibodies have made the transition from conception to clinical reality over the past two decades. Now, many of mAbs are being tested as adjuvant or first-line therapies to determine their efficacy in improving survival. In the future, the information drawn from genomemedical science and genome-informatics, that list the disease-related antigens useful for medical treatment, should be essential to develop the therapy using mAbs. Currently, the more attention is getting paid toward monoclonal antibody therapy. Several monoclonal antibodies, alone and in combination with other conventional therapies, are being tested in phase I and phase II clinical trials at the moment. Monoclonal antibody therapy can be done by using antibody fragments, antibody fusions with effector proteins and intrabodies. The large size and the long half-life of full-length antibody make them an inappropriate tool for radioimmunotherapy. Therefore, scientists produced some antibody fragments including scFv, Diabody and Nanobodies (sdAbs) which have smaller size besides maintaining the binding activity of the full-length molecule. Immunotoxin and Immunocytokines are consisting of toxin and cytokines fused to antibody fragments. An intrabody is produced by entering antibody into the cell and act against intracellular compartments. é 2013 - IOS Press and the authors. All rights reserved.
dc.language.isoEnglish
dc.relation.ispartofHuman Antibodies
dc.subjectcytokine
dc.subjectimmunocytokine
dc.subjectimmunotoxin
dc.subjectmonoclonal antibody
dc.subjectunclassified drug
dc.subjectantibody conjugate
dc.subjectantineoplastic agent
dc.subjecthybrid protein
dc.subjectimmunotoxin
dc.subjectmonoclonal antibody
dc.subjectnanobody
dc.subjectprotein binding
dc.subjecttumor antigen
dc.subjectadjuvant therapy
dc.subjectarticle
dc.subjectcancer immunotherapy
dc.subjectdrug indication
dc.subjecthuman
dc.subjectimmunotherapy
dc.subjectmalignant neoplastic disease
dc.subjectphase 1 clinical trial (topic)
dc.subjectphase 2 clinical trial (topic)
dc.subjectpriority journal
dc.subjectradioimmunotherapy
dc.subjectsurvival
dc.subjectantibody specificity
dc.subjectclinical trial (topic)
dc.subjecthalf life time
dc.subjectimmunology
dc.subjectNeoplasms
dc.subjectpathology
dc.subjectAntibodies, Monoclonal
dc.subjectAntibody Specificity
dc.subjectAntigens, Neoplasm
dc.subjectAntineoplastic Agents
dc.subjectClinical Trials as Topic
dc.subjectHalf-Life
dc.subjectHumans
dc.subjectImmunoconjugates
dc.subjectImmunotherapy
dc.subjectImmunotoxins
dc.subjectNeoplasms
dc.subjectProtein Binding
dc.subjectRecombinant Fusion Proteins
dc.subjectSingle-Domain Antibodies
dc.titleFuture prospects of monoclonal antibodies as magic bullets in Immunotherapy
dc.typeArticle
dc.citation.volume22
dc.citation.issue2
dc.citation.spage9
dc.citation.epage13
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.3233/HAB-130266


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