免疫疗法
癌症研究
癌症免疫疗法
抗体
癌症
肺癌
免疫系统
免疫检查点
癌细胞
PI3K/AKT/mTOR通路
靶向治疗
单克隆抗体
抗体-药物偶联物
医学
免疫学
生物
信号转导
细胞生物学
肿瘤科
内科学
作者
Tanmoy Saha,Michaela Fojtů,Astha Vinay Nagar,Liya Thurakkal,Balaaji Baanupriya Srinivasan,M. Mukherjee,Astralina Sibiyon,Heena Aggarwal,Akash Samuel,Chinmayee Dash,Hae Lin Jang,Shiladitya Sengupta
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2024-06-14
卷期号:10 (24)
被引量:15
标识
DOI:10.1126/sciadv.adi2046
摘要
The use of immune checkpoint inhibitors, which activate T cells, is a paradigm shift in the treatment of non–small cell lung cancer. However, the overall response remains low. To address this limitation, here we describe a novel platform, termed antibody-conjugated drug-loaded nanotherapeutics (ADN), which combines immunotherapy and molecularly targeted therapy. An ADN was designed with an anti-CD47 and anti–programmed death ligand 1 (PDL1) antibody pair on the surface of the nanoparticle and a molecularly targeted inhibitor of the PI3K (phosphatidylinositol 3-kinase)/AKT/mTOR (mammalian target of rapamycin) pathway, PI103, entrapped in the nanoparticle. The anti–CD47-PDL1-ADN exhibited greater antitumor efficacy than current treatment options with a PDL1 inhibitor in vivo in an aggressive lung cancer immunocompetent mouse model. Dual antibody-drug–loaded nanotherapeutics can emerge as an attractive platform to improve outcomes with cancer immunotherapy.
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