RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Impact of the source of hematopoietic stem cells on immune reconstitution after transplantation: A systematic review.
Impact of the source of hematopoietic stem cells on immune reconstitution after transplantation: A systematic review.
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造血干细胞(HSC)移植的成功在于其诱导免疫重建的能力。迄今为止,尚无综述比较三种HSC来源:脐带血(UCB)、骨髓(BM)和外周血(PB)之间的免疫重建。本综述旨在通过聚焦自然杀伤(NK)细胞、B淋巴细胞和T淋巴细胞以及中性粒细胞,分析UCB、PB和BM在HSC移植患者中免疫重建的动力学。通过五个数据库进行了系统综述,检索分析至少两种来源免疫重建动力学的临床试验和随机对照试验(RCT)。所选研究采用Cochrane RoB 2.0进行评估。本综述纳入14项研究,共2539名受试者。PB组中性粒细胞恢复时间最快,而UCB组B细胞计数最高。BM组T细胞计数最低,NK细胞计数在三种HSC来源之间无显著差异。在三种HSC来源中,对于任何免疫重建参数均无更优的HSC来源。必须开展更多研究,以比较特定疾病中所有HSC来源的免疫重建和临床结局。
Hematopoietic stem cell (HSC) transplantation's success lies in its ability to induce immune reconstitution. To date, there is no review published to compare the immune reconstitution among the three sources of HSC: umbilical cord blood (UCB), bone marrow (BM), and peripheral blood (PB). The review aims to analyze the kinetic of immune reconstitution among UCB, PB, and BM in HSC transplant patients by focusing on natural killer (NK) cells, B and T lymphocytes, and neutrophils. A systematic review was conducted through five databases, searching for clinical trials and randomized control trials (RCTs) which analyze the kinetics of immune reconstitution in at least two sources.
Selected studies were assessed with Cochrane RoB 2. 0. This review included 14 studies, with a total of 2539 subjects. The PB group achieved the fastest time to neutrophil recovery, while the B-cell count was the highest in the UCB group.
The T-cell count is the lowest in the BM group, and the NK-cell count does not differ significantly among the three HSC sources. Among the three sources of HSC, there is no superior HSC source for any immune reconstitution parameter. More studies must be conducted to compare the immune reconstitution and clinical outcomes of all HSC sources in specific diseases.
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