Preferential Regulatory T-Cell Generation from Memory CD4+ T-Cells Is Deficient During Acute Exacerbation of Multiple Sclerosis

dc.contributor.advisorNiederkorn, Jerry Y.en
dc.contributor.committeeMemberKarakndikar, Nitin J.en
dc.contributor.committeeMemberMohan, Chandraen
dc.contributor.committeeMemberGruchalla, Rebecca S.en
dc.creatorMohiuddin, Imran Hafizen
dc.date.accessioned2019-08-02T19:14:15Z
dc.date.available2019-08-02T19:14:15Z
dc.date.created2014-05
dc.date.issued2014-06-11
dc.date.submittedMay 2014
dc.date.updated2019-08-02T19:14:16Z
dc.descriptionThe general metadata -- e.g., title, author, abstract, subject headings, etc. -- is publicly available, but access to the submitted files is restricted to UT Southwestern campus access and/or authorized UT Southwestern users.en
dc.description.abstractMultiple sclerosis (MS) is an immune-mediated disease with reported defects in thymic T-cell output. Thymically-derived natural regulatory T-cells (nTregs) play a vital role in suppressing autoimmune responses. We have previously shown that, in humans, all activated T-cells attain transient FOXP3 expression that correlates with suppressive ability. In fact, peripheral generation of induced Tregs (iTregs) is likely the dominant source of regulatory cells in healthy adults and even more so in MS patients. Through the use of a sensitive flow-based suppression assay, we observed that memory and naïve CD4+CD25-FOXP3- T-cells both developed regulatory ability subsequent to a variety of activating stimuli. This suppressive ability was greater than that observed in nTregs and not explained by exhaustion of nutrients or competition for APCs. While blockade of activation using anti-IL-2, CTLA-4 Ig, anti-TGF-β, indomethacin or cyclosporin A did not affect iTreg generation, methotrexate preempted the induction of regulatory ability. Moreover, irradiation of iTregs also abrogated regulatory function. Interestingly, memory-derived CD25+ iTregs displayed significantly greater activation-induced FOXP3 induction compared to naïve counterparts, and exhibited significantly enhanced suppressive function per cell. Furthermore, the CD25- fraction of activated memory-derived iTregs also demonstrated regulatory function not observed in naïve counterparts. In particular, this induced regulatory population was present in both healthy controls and quiescent MS patients, but deficient during MS acute exacerbation. These studies suggest that iTreg development and function may vary dependent on precursor origin, and that clinical recovery from exacerbation to ix quiescence in MS is associated with a restoration of function in memory-derived CD4+CD25-FOXP3- Tregs.en
dc.format.mimetypeapplication/pdfen
dc.identifier.oclc1111292122
dc.identifier.urihttps://hdl.handle.net/2152.5/7062
dc.language.isoenen
dc.subjectCD4 Antigensen
dc.subjectForkhead Transcription Factorsen
dc.subjectImmunologic Memoryen
dc.subjectInterleukin-2 Receptor alpha Subuniten
dc.subjectMultiple Sclerosisen
dc.subjectT-Lymphocytes, Regulatoryen
dc.titlePreferential Regulatory T-Cell Generation from Memory CD4+ T-Cells Is Deficient During Acute Exacerbation of Multiple Sclerosisen
dc.typeThesisen
dc.type.materialtexten
thesis.degree.departmentGraduate School of Biomedical Sciencesen
thesis.degree.disciplineImmunologyen
thesis.degree.grantorUT Southwestern Medical Centeren
thesis.degree.levelDoctoralen
thesis.degree.nameDoctor of Philosophyen

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