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.
肿瘤细胞治疗研究
英文原题:Natural killer cell-derived exosomes for cancer immunotherapy: innovative therapeutics art.
Natural killer cell-derived exosomes for cancer immunotherapy: innovative therapeutics art.
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嵌合抗原受体NK 细胞(CAR-NK)推动了用于实体瘤和恶性肿瘤的现货型细胞治疗。然而,CAR-NK的发展因其免疫监视的不确定性和细胞毒性挑战而受到限制。NK 细胞来源的外泌体(NK-Exo)将NK细胞治疗的关键靶向细胞治疗与独特的无毒外泌体相结合,作为自体来源的穿梭载体用于癌症免疫治疗。本综述涵盖了细胞因子、过继性(自体及异体)NK免疫治疗、刺激性和调节性功能,以及来自NK细胞的无细胞衍生物。未来NK-Exo细胞毒性和抗肿瘤活性的路径,需考虑癌症免疫治疗中非caspase依赖/依赖的凋亡以及Fas/FasL通路。最后,详细讨论了NK-Exo治疗通过联合治疗的意义和启示,以及用于纯化和递送NK-Exo至严重免疫和肿瘤细胞及组织的新兴方法的发展。
Chimeric antigen receptor natural killer cells (CAR-NK) promote off-the-shelf cellular therapy for solid tumors and malignancy.
However,, the development of CAR-NK is due to their immune surveillance uncertainty and cytotoxicity challenge was restricted. Natural killer cell-derived exosome (NK-Exo) combine crucial targeted cellular therapies of NK cell therapies with unique non-toxic Exo as a self-origin shuttle against cancer immunotherapy.
This review study covers cytokines, adoptive (autologous and allogenic) NK immunotherapy, stimulatory and regulatory functions, and cell-free derivatives from NK cells. The future path of NK-Exo cytotoxicity and anti-tumor activity with considering non-caspase-independent/dependent apoptosis and Fas/FasL pathway in cancer immunotherapy.
Finally, the significance and implication of NK-Exo therapeutics through combination therapy and the development of emerging approaches for the purification and delivery NK-Exo to severe immune and tumor cells and tissues were discussed in detail.
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