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:KIR3DL3-HHLA2 and TMIGD2-HHLA2 pathways: The dual role of HHLA2 in immune responses and its potential therapeutic approach for cancer immunotherapy.
KIR3DL3-HHLA2 and TMIGD2-HHLA2 pathways: The dual role of HHLA2 in immune responses and its potential therapeutic approach for cancer immunotherapy.
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T细胞和自然杀伤(NK)细胞是免疫系统的重要组成部分,受共抑制和共刺激分子调控,其中B7家族和CD28家族发挥重要作用。既往针对B7/CD28家族成员(如PD-1)的免疫检查点研究已在肿瘤免疫治疗中取得显著成功。然而,仍需要寻找新的免疫检查点分子。近期研究表明,HHLA2通过在不同位点结合不同受体,对免疫系统发挥抑制和刺激功能。然而,HHLA2与其两个受体在T细胞和NK细胞之间的通路仍存在争议。
在此,我们综述了近期关于HHLA2配体与KIR3DL3和TMIGD2相互作用的研究。我们重点阐述了KIR3DL3/TMIGD2与HHLA2之间的通路及其在肿瘤进展中的功能。我们还探讨了HHLA2表达与癌症患者临床预后之间的关系。综述的关键科学概念:KIR3DL3/TMIGD2-HHLA2可能代表肿瘤微环境中的新通路,并作为开发针对人类癌症的新型治疗药物的重要免疫检查点。
BACKGROUND: T cells and natural killer (NK) cells are essential components of the immune system and are regulated by coinhibitory and costimulatory molecules in which the B7 family and CD28 family play significant roles. Previous immune checkpoint studies on B7/CD28 family members, such as PD-1, have led to remarkable success in cancer immunotherapy. However, there is still a need to find new immune checkpoint molecules. Recent studies have demonstrated that HHLA2 exerts inhibitory and stimulatory functions on the immune system by binding to different receptors on different sites. However, the pathways between HHLA2 and its two receptors on T cells and NK cells remain controversial. AIM OF REVIEW: Here, we reviewed recent studies about HHLA2 ligand interactions with KIR3DL3 and TMIGD2. We focused on elucidating the pathways between KIR3DL3/TMIGD2 and HHLA2 as well as their function in tumour progression. We also addressed the relationship between HHLA2 expression and the clinical prognosis of cancer patients. KEY SCIENTIFIC CONCEPTS OF REVIEW: KIR3DL3/TMIGD2-HHLA2 may represent novel pathways within the tumour microenvironment and serve as crucial immune checkpoints for developing novel therapeutic drugs against human cancer.
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