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dc.contributor.authorMansoori, B
dc.contributor.authorMohammadi, A
dc.contributor.authorShajari, N
dc.contributor.authorDavudian, S
dc.contributor.authorSalehi, S
dc.contributor.authorBaradaran, B
dc.date.accessioned2018-08-26T07:21:24Z
dc.date.available2018-08-26T07:21:24Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/46106
dc.description.abstractDespite using lots of progression in hypersensitivity, it is not yet a cure. Current treatment for allergy focuses on two approaches, including treats only the symptoms of allergy by utilizing drugs and the other is desensitization therapy (immunotherapy), which involves administration of specific allergens. The main obstacle to hypersensitivity permanent treatment is the IgE producing subclass of B-lymphocytes which is the source of IgE- producing in hypersensitive patients. Removal of these lymphocytes causes noticeable reduction in the levels of IgE and allergic responses significantly. In this paper, we proposed a novel complementary approach, which we have called the nano-liposomes-based target toxicity machine (NBTTM), which controls hypersensitivity by removing the IgE producing B-lymphocytes. In this regard, our proposed nano-liposomes (pollen allergens/Aptamer/SCFV/MIP loaded lipid bilayer enclosing toxin interior) will be able to bind to any IgE markers in the lymphatic circulation. The nano-liposomes will bind to the IgE+atopic B cells and cause cell death by internalizing into B cells.
dc.language.isoEnglish
dc.relation.ispartofARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY
dc.subjectAllergy
dc.subjectatopic disease
dc.subjectpollen allergens
dc.subjectMIP
dc.subjectnano-liposomes-based target toxicity machine (NBTTM)
dc.titleNano-liposome-based target toxicity machine: an alternative/complementary approach in atopic diseases
dc.typeArticle
dc.citation.volume45
dc.citation.issue7
dc.citation.spage1292
dc.citation.epage1297
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1080/21691401.2016.1261872


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