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针对多形性胶质母细胞瘤的自然杀伤细胞免疫治疗的潜在分子靶点。

Prospective Molecular Targets for Natural Killer Cell Immunotherapy against Glioblastoma Multiforme.

机构信息

Texas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.

Department of Microbiology, Immunology and Genetics, School of Biomedical Sciences, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.

出版信息

Cells. 2024 Sep 17;13(18):1567. doi: 10.3390/cells13181567.

Abstract

Glioblastoma multiforme (GBM) is the most common type of primary malignant brain tumor and has a dismal overall survival rate. To date, no GBM therapy has yielded successful results in survival for patients beyond baseline surgical resection, radiation, and chemotherapy. Immunotherapy has taken the oncology world by storm in recent years and there has been movement from researchers to implement the immunotherapy revolution into GBM treatment. Natural killer (NK) cell-based immunotherapies are a rising candidate to treat GBM from multiple therapeutic vantage points: monoclonal antibody therapy targeting tumor-associated antigens (TAAs), immune checkpoint inhibitors, CAR-NK cell therapy, Bi-specific killer cell engagers (BiKEs), and more. NK therapies often focus on tumor antigens for targeting. Here, we reviewed some common targets analyzed in the fight for GBM immunotherapy relevant to NK cells: EGFR, HER2, CD155, and IL-13Rα2. We further propose investigating the Lectin-like Transcript 1 (LLT1) and cell surface proliferating cell nuclear antigen (csPCNA) as targets for NK cell-based immunotherapy.

摘要

多形性胶质母细胞瘤(GBM)是最常见的原发性恶性脑肿瘤,总生存率极差。迄今为止,除了基线手术切除、放疗和化疗之外,没有任何 GBM 治疗方法能在患者的生存时间上取得成功。近年来,免疫疗法在肿瘤学领域掀起了一场风暴,研究人员也开始将免疫疗法革命引入 GBM 治疗。自然杀伤 (NK) 细胞为基础的免疫疗法是从多个治疗角度治疗 GBM 的新兴候选方法:针对肿瘤相关抗原 (TAA) 的单克隆抗体疗法、免疫检查点抑制剂、CAR-NK 细胞疗法、双特异性杀伤细胞衔接器 (BiKEs) 等。NK 疗法通常专注于肿瘤抗原进行靶向治疗。在这里,我们回顾了一些在 GBM 免疫治疗中与 NK 细胞相关的常见靶点:EGFR、HER2、CD155 和 IL-13Rα2。我们进一步提出将 Lectin-like Transcript 1 (LLT1) 和细胞表面增殖细胞核抗原 (csPCNA) 作为 NK 细胞为基础的免疫疗法的靶点进行研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3446/11429815/db35cd8cbbe2/cells-13-01567-g001.jpg

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