Thymic program directing the functional development of γδT17 Cells

dc.contributor.authorJouan, Youenn
dc.contributor.authorPatin, Emmanuel Christian
dc.contributor.authorHassane, Maya
dc.contributor.authorSi-Tahar, Mustapha
dc.contributor.authorBaranek, Thomas
dc.contributor.authorPaget, Christophe
dc.contributor.departmentBiochemistry and Molecular Genetics
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:37:57Z
dc.date.available2025-01-24T11:37:57Z
dc.date.issued2018
dc.description.abstractγδT cells comprise a unique T cell sublineage endowed with a wide functional repertoire, which allow them to play important-sometimes opposite-roles in many immune responses associated with infection, cancer, and inflammatory processes. This is largely dependent on the existence of pre-programmed discrete functional subsets that differentiate within the thymus at specific temporal windows of life. Since they represent a major early source of interleukin-17A in many models of immune responses, the γδT17 cell population has recently gained considerable interest. Thus, a better dissection of the developmental program of this effector γγδT subset appears critical in understanding their associated immune functions. Several recent reports have provided new exciting insights into the developmental mechanisms that control γδT cell lineage commitment and differentiation. Here, we review the importance of thymic cues and intrinsic factors that shape the developmental program of γδT17 cells. We also discuss the potential future areas of research in γδT17 cell development especially in regards to the recently provided data from deep RNA sequencing technology. Pursuing our understanding into this complex mechanism will undoubtedly provide important clues into the biology of this particular T cell sublineage. © 2018 Jouan, Patin, Hassane, Si-Tahar, Baranek and Paget.
dc.identifier.doihttps://doi.org/10.3389/fimmu.2018.00981
dc.identifier.eid2-s2.0-85046650638
dc.identifier.urihttp://hdl.handle.net/10938/28933
dc.language.isoen
dc.publisherFrontiers Media S.A.
dc.relation.ispartofFrontiers in Immunology
dc.sourceScopus
dc.subjectDevelopment
dc.subjectInnate immunity
dc.subjectInterleukin-17a
dc.subjectThymus
dc.subjectTranscription factor
dc.subjectΓδt cells
dc.subjectAutoimmune regulator protein
dc.subjectCd27 antigen
dc.subjectChemokine receptor ccr2
dc.subjectChemokine receptor ccr6
dc.subjectCyanocobalamin
dc.subjectEarly growth response factor 2
dc.subjectGamma interferon
dc.subjectInducible t cell costimulator ligand
dc.subjectInterleukin 17
dc.subjectInterleukin 6
dc.subjectIntrinsic factor
dc.subjectLymphotoxin beta receptor
dc.subjectMicrorna
dc.subjectNuclear receptor nur77
dc.subjectProstacyclin receptor
dc.subjectT lymphocyte receptor
dc.subjectTranscription factor sox4
dc.subjectTranscriptome
dc.subjectZinc finger and btb domain containing protein 16
dc.subjectBioinformatics
dc.subjectCell differentiation
dc.subjectCell interaction
dc.subjectCell maturation
dc.subjectCircadian rhythm
dc.subjectCytokine release
dc.subjectEffector cell
dc.subjectGamma delta t lymphocyte
dc.subjectHuman
dc.subjectImmune response
dc.subjectInflammation
dc.subjectLymphopoiesis
dc.subjectMicroenvironment
dc.subjectMucosal-associated invariant t cell
dc.subjectNeuroimmunology
dc.subjectOntogeny
dc.subjectReview
dc.subjectSequence analysis
dc.subjectSignal transduction
dc.subjectT lymphocyte
dc.subjectThymocyte
dc.subjectThymus function
dc.titleThymic program directing the functional development of γδT17 Cells
dc.typeReview

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