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 natural killer cells on outcomes after allogeneic hematopoietic stem cell transplantation: A systematic review and meta-analysis.
Impact of natural killer cells on outcomes after allogeneic hematopoietic stem cell transplantation: A systematic review and meta-analysis.
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NK 细胞对 HSCT 后的结局有有利影响。HSCT 后 NK 细胞输注的最佳使用方式可能是抢先式,以预防疾病复发。
自然杀伤(NK)细胞在同种异体造血干细胞移植(HSCT)后的早期免疫重建中发挥重要作用。
通过PubMed、Cochrane和ClinicalTrials.gov进行了截至2022年4月20日的文献检索。我们纳入了21项报告NK细胞对HSCT后结局影响数据的研究。数据提取遵循PRISMA指南。使用meta-package(Schwarzer等)进行汇总分析。计算了比例及95%置信区间(CI)。
我们纳入了来自21项研究的1785例患者,这些研究探讨了HSCT后NK细胞重建(8项研究/1455例患者)、干细胞移植物NK细胞含量(4项研究/185例患者)、HSCT后治疗性NK细胞输注(5项研究/74例患者)以及HSCT后抢先/预防性NK细胞输注(4项研究/77例患者)的影响。较高的NK细胞重建与更好的2年总生存期(OS)相关(高:77%,95%CI 0.73-0.82 vs 低:55%,95%CI 0.37-0.72;n=899),然而,由于数据不足,无法对复发率(RR)或移植物抗宿主病(GVHD)进行汇总分析。较高的移植物NK细胞含量显示出更好的汇总OS趋势(高:65.2%,95%CI 0.47-0.81 vs 低:46.5%,95%CI 0.24-0.70;n=157)、更低的RR(高:16.9%,95%CI 0.10-0.25 vs 低:33%,95%CI 0.04-0.72;n=157)以及更低的急性GVHD发生率(高:27.6%,95%CI 0.20-0.36 vs 低:49.7%,95%CI 0.26-0.74;n=157)。针对HSCT后血液学复发的治疗性NK或细胞因子诱导的杀伤(CIK)细胞输注报告,CIK细胞输注的总体缓解率(ORR)和完全缓解(CR)分别为48.9%和11%,NK细胞输注分别为82.8%和44.8%。在CIK和NK细胞输注患者中,分别观察到RR为55.6%和51.7%,急性GVHD为34.5%和20%,慢性GVHD为20.7%和11.1%。抢先性供者来源NK细胞输注以预防HSCT后复发具有良好结局,1年OS为69%,CR率为42%,ORR为77%,RR为28%,急性和慢性GVHD发生率分别为24.9%和3.7%。
Natural killer (NK) cells play a vital role in early immune reconstitution following allogeneic hematopoietic stem cell transplantation (HSCT).
A literature search was performed on PubMed, Cochrane, and Clinical trials.gov through April 20, 2022. We included 21 studies reporting data on the impact of NK cells on outcomes after HSCT. Data was extracted following the PRISMA guidelines. Pooled analysis was done using the meta-package (Schwarzer et al.). Proportions with 95% confidence intervals (CI) were computed.
We included 1785 patients from 21 studies investigating the impact of NK cell reconstitution post-HSCT (8 studies/1455 patients), stem cell graft NK cell content (4 studies/185 patients), therapeutic NK cell infusions post-HSCT (5 studies/74 patients), and pre-emptive/prophylactic NK cell infusions post-HSCT (4 studies/77 patients). Higher NK cell reconstitution was associated with a better 2-year overall survival (OS) (high: 77%, 95%CI 0.73-0.82 vs low: 55%, 95%CI 0.37-0.72; n=899), however, pooled analysis for relapse rate (RR) or graft versus host disease (GVHD) could not be performed due to insufficient data. Higher graft NK cell content demonstrated a trend towards a better pooled OS (high: 65.2%, 95%CI 0.47-0.81 vs low: 46.5%, 95%CI 0.24-0.70; n=157), lower RR (high: 16.9%, 95%CI 0.10-0.25 vs low: 33%, 95%CI 0.04-0.72; n=157), and lower acute GVHD incidence (high: 27.6%, 95%CI 0.20-0.36 vs low: 49.7%, 95%CI 0.26-0.74; n=157). Therapeutic NK or cytokine-induced killer (CIK) cell infusions for hematologic relapse post-HSCT reported an overall response rate (ORR) and complete response (CR) of 48.9% and 11% with CIK cell infusions and 82.8% and 44.8% with NK cell infusions, respectively. RR, acute GVHD, and chronic GVHD were observed in 55.6% and 51.7%, 34.5% and 20%, and 20.7% and 11.1% of patients with CIK and NK cell infusions, respectively. Pre-emptive donor-derived NK cell infusions to prevent relapse post-HSCT had promising outcomes with 1-year OS of 69%, CR rate of 42%, ORR of 77%, RR of 28%, and acute and chronic GVHD rates of 24.9% and 3.7%, respectively.
NK cells have a favorable impact on outcomes after HSCT. The optimal use of NK cell infusions post-HSCT may be in a pre-emptive fashion to prevent disease relapse.
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