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:Tumour-associated macrophages as a potential target to improve natural killer cell-based immunotherapies.
Tumour-associated macrophages as a potential target to improve natural killer cell-based immunotherapies.
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过继转移自然杀伤(NK)细胞已被提出作为一种新型免疫疗法,用于治疗对当前治疗方式耐药的恶性肿瘤。多项临床研究表明,NK 细胞输注耐受性良好,无严重副作用,并在血液系统恶性肿瘤中显示出有希望的结果。
然而,恶性实体瘤患者对这种疗法未显示出显著应答。这种令人失望的结果在很大程度上源于输注的 NK 细胞递送效率低下及其在肿瘤微环境(TME)中功能受损。肿瘤相关巨噬细胞(TAM)是大多数实体瘤 TME 中最丰富的基质细胞,高 TAM 密度与癌症患者预后不良相关。尽管我们对 TAM 与 NK 细胞之间相互作用的认识有限,但许多研究表明 TAM 抑制 NK 细胞对癌细胞的细胞毒性。
因此,阻断 TAM 功能可能是改善基于 NK 细胞的免疫疗法的一个有吸引力的策略。另一方面,据报道巨噬细胞在某些情况下可激活 NK 细胞。本文介绍了我们目前关于巨噬细胞调节 NK 细胞功能机制的认识,并讨论了阻断巨噬细胞介导的 NK 细胞抑制的可能治疗途径。
Adoptive transfer of natural killer (NK) cells has been proposed as a novel immunotherapy for malignant tumours resistant to current therapeutic modalities. Several clinical studies have demonstrated that the NK cell-infusion is well tolerated without severe side effects and shows promising results in haematological malignancies.
However, patients with malignant solid tumours do not show significant responses to this therapy. Such disappointing results largely arise from the inefficient delivery of infused NK cells and the impairment of their functions in the tumour microenvironment (TME).
Tumour-associated macrophages (TAMs) are the most abundant stromal cells in the TME of most solid tumours, and a high TAM density correlates with poor prognosis of cancer patients. Although our knowledge of the interactions between TAMs and NK cells is limited, many studies have indicated that TAMs suppress NK cell cytotoxicity against cancer cells.
Therefore, blockade of TAM functions can be an attractive strategy to improve NK cell-based immunotherapies. On the other hand, macrophages are reported to activate NK cells under certain circumstances. This essay presents our current knowledge about mechanisms by which macrophages regulate NK cell functions and discusses possible therapeutic approaches to block macrophage-mediated NK cell suppression.
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