工程化益生菌用于肿瘤靶向联合化学免疫治疗
Engineered probiotics for tumor-targeted combination chemoimmunotherapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:CAR-macrophages in solid tumors: promise, progress, and prospects.
CAR-macrophages in solid tumors: promise, progress, and prospects.
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嵌合抗原受体巨噬细胞(CAR-Ms)代表了免疫治疗中一个前景广阔的前沿领域,利用先天性和工程化能力来对抗实体瘤。CAR-Ms能够主动重塑肿瘤微环境,同时通过CAR信号直接靶向肿瘤细胞,使其成为现有基于细胞的疗法的潜在替代方案。临床前和临床证据表明,CAR-M疗法在治疗实体瘤方面具有重大前景。然而,由于细胞扩增受限、基因工程复杂性以及产品质量的变异性,其临床转化仍面临挑战。本文综述了CAR-M领域的最新进展,讨论了该方法背后的生物学原理、关键临床前发现,以及为促进其作为针对难以治疗的实体恶性肿瘤的通用、即用型免疫疗法取得临床成功所必需的技术创新。
Chimeric antigen receptor macrophages (CAR-Ms) represent a promising frontier in immunotherapy, leveraging both innate and engineered capabilities to combat solid tumors. CAR-Ms can actively remodel the tumor microenvironment while directly targeting tumor cells through CAR signaling, making them a potential alternative to existing cell-based therapies. Pre-clinical and clinical evidence suggests that CAR-M therapy holds significant promise for treating solid tumors.
However, its clinical translation remains challenging due to restricted cell expansion, genetic engineering complexities, and variability in product quality. This article reviews recent advances in the CAR-M field, discussing the biological rationale behind this approach, key preclinical findings, and technological innovations necessary to facilitate clinical success as a versatile, off the shelf immunotherapy for hard-to-treat solid malignancies.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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