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:Effects of perioperative low-dose naloxone on the immune system in patients undergoing laparoscopic-assisted total gastrectomy: a randomized controlled trial.
Effects of perioperative low-dose naloxone on the immune system in patients undergoing laparoscopic-assisted total gastrectomy: a randomized controlled trial.
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腹腔镜全胃切除术患者可能从 0.05 μg/kg·h⁻¹纳洛酮中获益,从而降低其感染风险。LDN 可能改变淋巴细胞亚群中的细胞数量,如 NK 细胞、CD3+ T 细胞和 CD4+ T 细胞,以及 CD4+/CD8+ T 细胞比值,或改变免疫细胞中 TLR4 受体的表达,从而改变免疫细胞活性。
腹腔镜全胃切除术后免疫功能低下使患者面临感染相关并发症的风险。低剂量纳洛酮(LDN)可改善慢性炎症性疾病或自身免疫性疾病患者的预后。围手术期使用LDN可能减少围手术期并发症。本研究的目的是通过随机对照试验探讨LDN对胃癌患者内源性免疫功能的影响及其具体机制。
55例接受腹腔镜辅助全胃切除术的患者被随机分配到纳洛酮组(n=23)或非纳洛酮组(n=22)。纳洛酮组患者从术前3天到术后5天通过患者自控静脉注射(PCIA)泵接受0.05 g/kg-1.h-1纳洛酮,非纳洛酮组患者未接受特殊治疗。主要结局是术后并发症发生率和免疫功能,通过NK细胞、CD3+T细胞、CD4+T细胞、CD8+T细胞、WBC计数、中性粒细胞百分比以及IL-6和降钙素水平评估。次要结局是胃癌组织中TLR4(Toll样受体)、IL-6和TNF-的表达水平。
与未使用纳洛酮组相比,纳洛酮组感染(切口、腹腔和肺部)发生率较低(P < 0.05)。术后24 h(P < 0.05)和术后96 h(P < 0.05),纳洛酮组NK细胞和CD8 + T细胞数量显著多于未使用纳洛酮组。与未使用纳洛酮组相比,术后24 h纳洛酮组CD3 + T细胞(P < 0.05)和CD4 + T细胞(P < 0.01)计数显著较低。术后24 h和96 h,未使用纳洛酮组WBC计数(P < 0.05)和中性粒细胞百分比(P < 0.05)显著较高。术后24 h,未使用纳洛酮组IL-6(P < 0.05)和降钙素水平显著较高。术后24 h,未使用纳洛酮组IL-6(P < 0.05)和降钙素水平显著高于纳洛酮组。与纳洛酮组相比,纳洛酮组胃癌组织中TLR4(P < 0.05)表达水平较高;然而,纳洛酮组IL-6(P < 0.01)和TNF-(P < 0.01)表达水平高于未使用纳洛酮组。
Low immune function after laparoscopic total gastrectomy puts patients at risk of infection-related complications. Low-dose naloxone (LDN) can improve the prognosis of patients suffering from chronic inflammatory diseases or autoimmune diseases. The use of LDN during perioperative procedures may reduce perioperative complications. The purpose of this study was to examine the effects of LDN on endogenous immune function in gastric cancer patients and its specific mechanisms through a randomized controlled trial.
Fifty-five patients who underwent laparoscopic-assisted total gastrectomy were randomly assigned to either a naloxone group (n = 23) or a nonnaloxone group (n = 22). Patients in the naloxone group received 0.05 g/kg-1.h - 1 naloxone from 3 days before surgery to 5 days after surgery via a patient-controlled intravenous injection (PCIA) pump, and patients in the nonnaloxone group did not receive special treatment. The primary outcomes were the rates of postoperative complications and immune function assessed by NK cell, CD3 + T cell, CD4 + T cell, CD8 + T cell, WBC count, neutrophil percentage, and IL-6 and calcitonin levels. The secondary outcomes were the expression levels of TLR4 (Toll-like receptor), IL-6 and TNF- in gastric cancer tissue.
Compared with the nonnaloxone group, the naloxone group exhibited a lower incidence of infection (in the incision, abdomen, and lungs) (P < 0.05). The numbers of NK cells and CD8 + T cells in the naloxone group were significantly greater than those in the nonnaloxone group at 24 h after surgery (P < 0.05) and at 96 h after surgery (P < 0.05). Compared with those in the nonnaloxone group, the CD3 + T-cell (P < 0.05) and CD4 + T-cell (P < 0.01) counts were significantly lower in the naloxone group 24 h after surgery. At 24 h and 96 h after surgery, the WBC count (P < 0.05) and neutrophil percentage (P < 0.05) were significantly greater in the nonnaloxone group. The levels of IL-6 (P < 0.05) and calcitonin in the nonnaloxone group were significantly greater at 24 h after surgery. At 24 h following surgery, the nonnaloxone group had significantly greater levels of IL-6 (P < 0.05) and calcitonin than did the naloxone group. Compared with those in the naloxone group, the expression levels of TLR4 (P < 0.05) in gastric cancer tissue in the naloxone group were greater; however, the expression levels of IL-6 (P < 0.01) and TNF- (P < 0.01) in the naloxone group were greater than those in the nonnaloxone group.
Laparoscopic total gastrectomy patients can benefit from 0.05 ug/kg - 1 . h - 1 naloxone by reducing their risk of infection. It is possible that LDN alters the number of cells in lymphocyte subpopulations, such as NK cells, CD3 + T cells, and CD4 + T cells, and the CD4 + /CD8 + T-cell ratio or alters TLR4 receptor expression in immune cells, thereby altering immune cell activity. TRIAL REGISTRATION: The trial was registered at the Chinese Clinical Trial Registry on 24/11/2023 (ChiCTR2300077948).
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