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:Expanded clinical-grade NK cells exhibit stronger effects than primary NK cells against HCMV infection.
Expanded clinical-grade NK cells exhibit stronger effects than primary NK cells against HCMV infection.
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巨细胞病毒(CMV)再激活仍然是接受异基因造血干细胞移植(allo-HSCT)患者的常见并发症,并导致高死亡率。早期自然杀伤(NK)细胞重建可能有助于预防HSCT后发生人CMV(HCMV)感染。
我们之前的数据显示,经体外mbIL21/4-1BBL扩增的NK细胞对白血病细胞表现出高细胞毒性。然而,扩增NK细胞是否具有更强的抗HCMV功能尚不清楚。
在此,我们比较了体外扩增NK细胞与原代NK细胞的抗HCMV功能。与原代NK细胞相比,扩增NK细胞表现出更高的激活性受体、趋化因子受体和黏附分子表达;对HCMV感染成纤维细胞更强的细胞毒性;以及在体外对HCMV增殖更好的抑制作用。在HCMV感染的人源化小鼠中,输注扩增NK细胞比输注原代NK细胞带来更高的NK细胞持久性,并更有效地清除组织中的HCMV。在一个由20例接受过过继性NK细胞输注的HSCT后患者组成的临床队列中,与对照组相比,HCMV感染(HR = 0.54,95% CI = 0.32-0.93,p = 0.042)和难治性HCMV感染(HR = 0.34,95% CI = 0.18-0.65,p = 0.009)的累积发生率显著更低,并且在NK细胞输注后第30天具有更好的NK细胞重建。
总之,扩增NK细胞在体内和体外均比原代NK细胞表现出更强的抗HCMV感染作用。
Cytomegalovirus (CMV) reactivation remains a common complication and leads to high mortality in patients who undergo allogeneic hematopoietic stem cell transplantation (allo-HSCT). Early natural killer (NK) cell reconstitution may protect against the development of human CMV (HCMV) infection post-HSCT.
Our previous data showed that ex vivo mbIL21/4-1BBL-expanded NK cells exhibited high cytotoxicity against leukemia cells. Nevertheless, whether expanded NK cells have stronger anti-HCMV function is unknown.
Herein, we compared the anti-HCMV functions of ex vivo expanded NK cells and primary NK cells. Expanded NK cells showed higher expression of activating receptors, chemokine receptors and adhesion molecules; stronger cytotoxicity against HCMV-infected fibroblasts; and better inhibition of HCMV propagation in vitro than primary NK cells. In HCMV-infected humanized mice, expanded NK cell infusion resulted in higher NK cell persistence and more effective tissue HCMV elimination than primary NK cell infusion.
A clinical cohort of 20 post-HSCT patients who underwent adoptive NK cell infusion had a significantly lower cumulative incidence of HCMV infection (HR = 0. 54, 95% CI = 0. 32-0. 93, p = 0. 042) and refractory HCMV infection (HR = 0. 34, 95% CI = 0. 18-0. 65, p = 0. 009) than controls and better NK cell reconstitution on day 30 post NK cell infusion.
In conclusion, expanded NK cells exhibit stronger effects than primary NK cells against HCMV infection both in vivo and in vitro.
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