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dc.rights.licenseCC-BY-NC-ND
dc.contributor.advisorBeekman, J.
dc.contributor.authorShaltiël, I.A.
dc.date.accessioned2009-02-03T18:00:49Z
dc.date.available2009-02-03
dc.date.available2009-02-03T18:00:49Z
dc.date.issued2009
dc.identifier.urihttps://studenttheses.uu.nl/handle/20.500.12932/2402
dc.description.abstractHelper T lymphocytes are master regulators of the adaptive immune response. Recent years have demonstrated the existence of four functionally distinct effector subsets: type 1, type 2, regulatory and IL-17 producing T helper cells. Manipulation of T helper cell differentiation may prove useful for effective vaccine development and treatment of allergic and autoimmune diseases. Here, I discuss which signals control T helper cell lineage commitment, how these multiple signals are integrated during the polarisation process and subsequent cross-regulatory mechanisms that effectuate lineage stabilisation, affording new insights into the role of T cell receptor-mediated and co-stimulatory signals in T helper cell polarisation and the role of suppressors of cytokine signalling (SOCS) family members in lineage stabilisation.
dc.description.sponsorshipUtrecht University
dc.format.extent1335995 bytes
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.titleGetting the message through; signal transduction and integration in T helper cell lineage commitment
dc.type.contentMaster Thesis
dc.rights.accessrightsOpen Access
dc.subject.keywordsT helper cell
dc.subject.keywordsCD4
dc.subject.keywordslymphocyte differentiation
dc.subject.keywordspolarisation
dc.subject.keywordsTh1
dc.subject.keywordsTh2
dc.subject.keywordsregulatory T cell
dc.subject.keywordsFoxp3
dc.subject.keywordsT-bet
dc.subject.keywordsGata3
dc.subject.keywordsRorc
dc.subject.courseuuImmunity and Infection


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