Fetal-derived activated CD83+ γδ T cells expand in preterm infants with sepsis.
收藏NIAID Data Ecosystem2026-05-02 收录
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE245131
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Here, we investigated γδ T cells in a longitudinal cohort of preterm neonates during the first year of life. Our data reveal dynamic postnatal maturation patterns of γδ T cell subsets, which are largely age-dependent. We report on the expansion of fetal-derived γδ T cells in preterm neonates with sepsis. Single cell transcriptome analyses identified HLA-DRhigh and CD83+ γδ T cells in neonatal sepsis. Combined single-cell transcriptome (scRNA-seq) and single-cell γδTCR-seq (scTCR-seq) analysis was conducted from peripheral blood.
本研究针对出生后第一年的早产新生儿纵向队列,对γδ T细胞(γδ T cell)展开了系统性探究。研究数据揭示了γδ T细胞亚群呈现出动态的出生后成熟模式,该模式在很大程度上依赖于年龄。本研究还报道了合并脓毒症的早产新生儿体内,胎儿源性γδ T细胞发生扩增的现象。单细胞转录组分析在新生儿脓毒症样本中,鉴定出了HLA-DR高表达(HLA-DRhigh)与CD83阳性(CD83+)的γδ T细胞亚群。研究同时对外周血样本开展了单细胞转录组测序(scRNA-seq)与单细胞γδ T细胞受体测序(scTCR-seq)的联合分析。
创建时间:
2024-10-16



