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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Age-related impaired type 1 T cell responses to influenza: reduced activation ex vivo, decreased expansion in CTL culture in vitro, and blunted response to influenza vaccination in vivo in the elderly.
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Age-related impaired type 1 T cell responses to influenza: reduced activation ex vivo, decreased expansion in CTL culture in vitro, and blunted response to influenza vaccination in vivo in the elderly.

机译:年龄相关的1型T细胞对流感的反应减弱:离体激活减少,体外CTL培养物中扩增减少,老年人体内对流感疫苗接种的反应减弱。

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摘要

The objective of this study was to analyze the changes in the type 1 T cell response, including the CD4+ Th1 and CD8+ T cell responses, to influenza in the elderly compared with those in young adults. PBMC activated ex vivo with influenza virus exhibited an age-related decline in type 1 T cell response, shown by the decline in the frequency of IFN-gamma-secreting memory T cells specific for influenza (IFN-gamma+ ISMT) using ELISPOT or intracellular cytokine staining. The reduced frequency of IFN-gamma+ ISMT was accompanied by a reduced level of IFN-gamma secretion per cell in elderly subjects. Tetramer staining, combined with IFN-gamma ELISPOT, indicated that the decline in IFN-gamma+, influenza M1-peptide-specific T cells was not due to attrition of the T cell repertoire, but, rather, to the functional loss of ISMT with age. In addition, the decline in type 1 T cell response was not due to an increase in Th2 response or defects in APCs from the elderly. The expansion of influenza-specific CD8+ T cellsin CTL cultures was reduced in the elderly. Compared with young subjects, frail elderly subjects also exhibited a blunted and somewhat delayed type 1 T cell response to influenza vaccination, which correlated positively with the reduced IgG1 subtype and the total Ab response. Taken together, these data demonstrate that there is a decline in the type 1 T cell response to influenza with age that may help explain the age-related decline in vaccine efficacy and the increases in influenza morbidity and mortality.
机译:这项研究的目的是分析与年轻人相比,老年人对流感的1型T细胞应答(包括CD4 + Th1和CD8 + T细胞应答)的变化。用流感病毒离体激活的PBMC在1型T细胞应答中表现出与年龄相关的下降,这表现为使用ELISPOT或细胞内细胞因子对流感特异的IFN-γ分泌性记忆T细胞(IFN-γ+ ISMT)的频率下降染色。 IFN-γ+ ISMT频率的降低伴随着老年受试者每个细胞中IFN-γ分泌水平的降低。四聚体染色与IFN-γELISPOT结合使用,表明IFN-γ+流感M1肽特异性T细胞的下降不是由于T细胞库的损耗,而是由于ISMT随着年龄的增长而功能丧失。此外,1型T细胞应答的下降并不是由于Th2应答增加或老年人的APC缺陷。老年人中,CTL培养物中流感特异性CD8 + T细胞的扩增减少。与年轻受试者相比,年老体弱的受试者对流感疫苗的接种还表现出钝钝的1型T细胞反应,这与IgG1亚型减少和总Ab反应呈正相关。综上所述,这些数据表明,随着年龄的增长,对流感的1型T细胞反应有所下降,这可能有助于解释与年龄相关的疫苗效力下降以及流感发病率和死亡率的上升。

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