Journal of Leukocyte Biology: An Official Publication of the Reticuloendothelial Society | |
The impact of aging on memory T cell phenotype and function in the human bone marrow | |
关键词: CD8+CD28–; T cell; IL‐; 15; IL‐; 6; CD57; inflamm‐; aging; cytomegalovirus infection; | |
DOI : 10.1189/jlb.0611299 | |
学科分类:生理学 | |
来源: Federation of American Societies for Experimental Biology | |
【 摘 要 】
Recently,theBMhasbeenshowntoplayakeyroleinregulatingthesurvivalandfunctionofmemoryTcells.However,theimpactofagingontheseprocesseshasnotyetbeenstudied.WedemonstratethatthenumberofCD4+andCD8+TcellsintheBMismaintainedduringaging.However,thecompositionoftheTcellpoolintheagedBMisalteredwithadeclineofnaïveandanincreaseinTEMcells.IncontrasttothePB,ahighlyactivatedCD8+CD28–Tcellpopulation,whichlacksthelatedifferentiationmarkerCD57,accumulatesintheBMofelderlypersons.IL‐6andIL‐15,whicharebothincreasedintheagedBM,efficientlyinducetheactivation,proliferation,anddifferentiationofCD8+Tcellsinvitro,highlightingaroleofthesecytokinesintheage‐dependentaccumulationofhighlyactivatedCD8+CD28–TcellsintheBM.Yet,theseage‐relatedchangesdonotimpairthemaintenanceofahighnumberofpolyfunctionalmemoryCD4+andCD8+TcellsintheBMofelderlypersons.Insummary,agingleadstotheaccumulationofahighlyactivatedCD8+CD28–TcellpopulationintheBM,whichisdrivenbytheage‐relatedincreaseofIL‐6andIL‐15.Despitethesechanges,theagedBMisarichsourceofpolyfunctionalmemoryTcellsandmaythusrepresentanimportantlineofdefensetofightrecurrentinfectionsinoldage...
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