The Patrick G Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, UK, BT9 7AE.
Cancer Research UK Manchester Institute, Alderley Park, Congleton Rd, Alderley Edge, Macclesfield, UK, SK10 4TG.
Nanoscale. 2021 Sep 17;13(35):15010-15020. doi: 10.1039/d1nr04001d.
For effective targeted therapy of cancer with chemotherapy-loaded nanoparticles (NPs), antigens that are selective for cancer cells should be targeted to minimise off-tumour toxicity. Human leukocyte antigens (HLAs) are attractive cancer targets as they can present peptides from tumour-selective proteins on the cell surface, which can be recognised by T cells T cell receptors (TCRs). In this study, docetaxel-loaded polymeric NPs were conjugated to recombinant affinity-enhanced TCRs to target breast cancer cells presenting a tumour-selective peptide-HLA complex. The TCR-conjugated nanoparticles enabled enhanced delivery of docetaxel and induced cell death through tumour-specific peptide-HLA targeting. These data demonstrate the potential of targeting tumour-restricted peptide-HLA epitopes using high affinity TCR-conjugated nanoparticles, representing a novel treatment strategy to deliver therapeutic drugs specifically to cancer cells.
为了通过载化疗药物的纳米颗粒(NPs)进行有效的癌症靶向治疗,应将针对肿瘤细胞的抗原靶向,以最大程度减少肿瘤外毒性。人类白细胞抗原(HLAs)是有吸引力的癌症靶点,因为它们可以在细胞表面呈现来自肿瘤选择性蛋白的肽,这些肽可以被 T 细胞 T 细胞受体(TCRs)识别。在这项研究中,多西紫杉醇负载的聚合物 NPs 与重组亲和力增强的 TCR 连接,以靶向呈递肿瘤选择性肽-HLA 复合物的乳腺癌细胞。TCR 偶联的纳米颗粒能够增强多西紫杉醇的递送,并通过肿瘤特异性肽-HLA 靶向诱导细胞死亡。这些数据表明,使用高亲和力 TCR 偶联的纳米颗粒靶向肿瘤限制性肽-HLA 表位具有潜力,为将治疗药物特异性递送至癌细胞提供了一种新的治疗策略。