← 返回

递送检查点抑制剂调节剂的工程化食源性益生菌

英文原题:Engineered food-borne probiotics delivering checkpoint-inhibitor modulators.

查看英文原题

Engineered food-borne probiotics delivering checkpoint-inhibitor modulators.

PubMed 2025/12/03(内容时间) Ann Med Surg (Lond) Q2 · IF 1.6(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

工程化食源性益生菌是一种新兴的“食品—肿瘤微生物学”策略,融合合成生物学、营养学和癌症免疫治疗。临床前模型显示出强效抗肿瘤作用:分泌可溶性CD80的乳酸乳球菌使肿瘤生长降低64%;产生PD-L1纳米抗体的大肠杆菌Nissle 1917使50%的治疗小鼠肿瘤完全消退,并使CD8⁺ IFN/TNF T细胞浸润增加一倍;递送IL-2的植物乳杆菌使NK细胞活性提高2.5倍、生存延长30%。临床荟萃分析显示,肠道微生物组多样性可使免疫检查点抑制剂缓解率提高40%、中位无进展生存期延长12个月。一项非小细胞肺癌(NSCLC)I期试验显示,益生菌联合治疗使免疫相关结肠炎发生率从14%降至6%,缓解率从21%升至36%。定植和生物安全方面的挑战仍待解决;与此同时,可控基因线路的发展使可食用生物制剂成为一种有前景、低毒性的免疫治疗平台。

展开英文摘要原文

Engineered food-borne probiotics represent an emerging food-oncomicrobiology strategy that unites synthetic biology, nutrition, and cancer immunotherapy. Preclinical models demonstrate potent antitumor effects: Lactococcus lactis secreting soluble CD80-reduced tumor growth by 64%; Escherichia coli Nissle 1917 producing PD-L1 nanobodies achieved complete regression in 50% of treated mice with a two-fold rise in CD8 IFN TNF T-cell infiltration; and Lactobacillus plantarum delivering IL-2 enhanced NK-cell activity 2.

5-fold and extended survival by 30%. Clinical meta-analyses reveal that gut-microbiome diversity increases checkpoint-inhibitor response by 40% and median progression-free survival by 12 months. A phase I trial in Non-Small Cell Lung Cancer (NSCLC) showed reduced immune-related colitis (from 14% to 6%) and higher response rates (36% vs 21%) with probiotic co-therapy. Remaining challenges in colonization and biosafety, together with advances in controllable genetic circuits, make edible biologics a promising, low-toxicity immunotherapeutic platform.

论文信息

作者
Mehmood MS、Masood M、Danaf N
第一作者单位
Faculty of Veterinary Science, Institute of Microbiology, University of Agriculture Faisalabad, Faisalabad, Pakistan.
通讯作者单位
Faculty of Medical Sciences, Lebanese University, Beirut P.O. Box 6573/14, Lebanon.
文献类型
社论
期刊
Annals of medicine and surgery (2012)2026 Jan
原文标识
PubMed 41497008 · DOI 10.1097/MS9.0000000000004399