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Antibody nanoparticle conjugate-based targeted immunotherapy for non-small cell lung cancer
被引:8
|作者:
Saha, Tanmoy
[1
,2
]
Fojtu, Michaela
[1
,2
]
Nagar, Astha Vinay
[1
,2
]
Thurakkal, Liya
[1
,2
]
Srinivasan, Balaaji Baanupriya
[1
,2
]
Mukherjee, Meghma
[1
,2
]
Sibiyon, Astralina
[1
,2
]
Aggarwal, Heena
[1
,2
]
Samuel, Akash
[1
,2
]
Dash, Chinmayee
[1
,2
]
Jang, Hae Lin
[2
,3
,4
]
Sengupta, Shiladitya
[1
,2
,5
,6
]
机构:
[1] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Div Engn Med, Boston, MA 02115 USA
[2] Harvard Med Sch, Brigham & Womens Hosp, Ctr Engn Therapeut, Dept Med, Boston, MA 02115 USA
[3] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Div Rheumatol Inflammat & Immun, Boston, MA USA
[4] Harvard Med Sch, Brigham & Womens Hosp, Dept Orthopaed Surg, Boston, MA USA
[5] Harvard MIT Program Hlth Sci & Technol, Cambridge, MA 02139 USA
[6] Dana Farber Canc Inst, Boston, MA 02215 USA
来源:
SCIENCE ADVANCES
|
2024年
/
10卷
/
24期
关键词:
CD47;
RESISTANCE;
PD-L1;
PEMBROLIZUMAB;
CHEMOTHERAPY;
EXPRESSION;
BLOCKADE;
EFFICACY;
PATHWAY;
D O I:
10.1126/sciadv.adi2046
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
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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页数:15
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