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Phenotypic and functional analyses of NK and NKT-like populations during the early stages of chikungunya infection

机译:基孔肯雅热感染初期NK和NKT样人群的表型和功能分析

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The aim of this study was to characterize NK (CD56~(+)CD3~(?)) and NKT-like cell (CD56~(+)CD3~(+)) responses early after chikungunya infection. Expression profiling and functional analysis of T/NK/NKT-like cells were performed on samples from 56 acute and 31 convalescent chikungunya patients and 56 control individuals. The percentages of NK cells were high in both patient groups, whereas NKT-like cell percentages were high only in the convalescent group. The percentages of NKp30~(+)CD3~(?)CD56~(+), NKp30~(+)CD3~(+)CD56~(+), CD244~(+)CD3~(?)CD56~(+), and CD244~(+)CD3~(+)CD56~(+)cells were high, whereas the percentages of NKG2D~(+)CD3~(?)CD56~(+)and NKG2D~(+)CD3~(+)CD56~(+)cells were low in both patient groups. The percentages of NKp44~(+)CD3~(?)CD56~(+)cells were high in both patient groups, whereas the percentages of NKp44~(+)CD3~(+)CD56~(+)cells were higher in the acute group than in convalescent and control groups. The percentages of NKp46~(+)CD3~(?)CD56~(+)cells were high in both patient groups. Higher percentages of perforin~(+)CD3~(?)CD56~(+)and perforin~(+)CD3~(+)CD56~(+)cells were observed in acute and convalescent patients, respectively. Higher cytotoxic activity was observed in acute patients than in controls. IFN-γ expression on NK cells of convalescent patients and on NKT-like cells of both patient groups was indicative of the regulatory role of NK and NKT-like cells. Collectively, these data showed that higher expression of activating receptors on NK/NKT-like cells and perforin~(+)NK cells in acute patients could be responsible for increased cytotoxicity. The observed expression of perforin~(+)NK cells in the acute phase and IFN-γ~(+)NKT-like cells in the subsequent convalescent stage showed that NK/NKT-like cells mount an early and efficient response to chikungunya virus. Further study of the molecular mechanisms that limit viral dissemination/establishment of chronic disease will aid in understanding how NK/NKT-like cells control chikungunya infection.
机译:本研究的目的是在基孔肯雅病感染后早期表征NK(CD56〜(+)CD3〜(+))和NKT样细胞(CD56〜(+)CD3〜(+))的反应。 T / NK / NKT样细胞的表达谱分析和功能分析来自56例急性和31例恢复期基孔肯雅热患者和56例对照个体。在两个患者组中,NK细胞的百分比均较高,而仅在恢复期组中,NKT样细胞的百分比较高。 NKp30〜(+)CD3〜(?)CD56〜(+),NKp30〜(+)CD3〜(+)CD56〜(+),CD244〜(+)CD3〜(?)CD56〜(+)的百分比,CD244〜(+)CD3〜(+)CD56〜(+)细胞较高,而NKG2D〜(+)CD3〜(?)CD56〜(+)和NKG2D〜(+)CD3〜(+两组患者CD56〜(+)细胞均较低。两组患者中NKp44〜(+)CD3〜(?)CD56〜(+)细胞的百分比均较高,而NKp44〜(+)CD3〜(+)CD56〜(+)细胞的百分比较高。急性期较康复期和对照组多。两组患者中NKp46〜(+)CD3〜(?)CD56〜(+)细胞的百分比均较高。在急性和恢复期患者中,perforin〜(+)CD3〜(α)CD56〜(+)和perforin〜(+)CD3〜(+)CD56〜(+)细胞的百分比更高。在急性患者中观察到的细胞毒性活性高于对照组。恢复期患者的NK细胞和两个患者组的NKT样细胞上的IFN-γ表达指示NK和NKT样细胞的调节作用。总体而言,这些数据表明,急性患者中NK / NKT样细胞和perforin〜(+)NK细胞上活化受体的较高表达可能是细胞毒性增加的原因。观察到急性期穿孔素〜(+)NK细胞和随后恢复期的IFN-γ〜(+)NKT样细胞的表达表明,NK / NKT样细胞对基孔肯雅病毒具有早期和有效的反应。限制病毒传播/建立慢性疾病的分子机制的进一步研究将有助于理解NK / NKT样细胞如何控制基孔肯雅热感染。

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