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Laser Immunotherapy in Combination with Perdurable PD‑1 Blocking for the Treatment of Metastatic Tumors

A convenient and feasible therapeutic strategy for malignant and metastatic tumors was constructed here by combining photothermal ablation (PTA)-based laser immunotherapy with perdurable PD-1 blockade immunotherapy. Hollow gold nanoshells (HAuNS, a photothermal agent) and AUNP12 (an anti PD-1 peptid...

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Published in:ACS nano 2018-08, Vol.12 (8), p.7647-7662
Main Authors: Luo, Lihua, Zhu, Chunqi, Yin, Hang, Jiang, Mengshi, Zhang, Junlei, Qin, Bing, Luo, Zhenyu, Yuan, Xiaoling, Yang, Jie, Li, Wei, Du, Yongzhong, You, Jian
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cited_by cdi_FETCH-LOGICAL-a333t-d0c56f23c6cc32286a3f989a7ae69f8ebd32990332d52d813e0a83f2a77cd57a3
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container_issue 8
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container_title ACS nano
container_volume 12
creator Luo, Lihua
Zhu, Chunqi
Yin, Hang
Jiang, Mengshi
Zhang, Junlei
Qin, Bing
Luo, Zhenyu
Yuan, Xiaoling
Yang, Jie
Li, Wei
Du, Yongzhong
You, Jian
description A convenient and feasible therapeutic strategy for malignant and metastatic tumors was constructed here by combining photothermal ablation (PTA)-based laser immunotherapy with perdurable PD-1 blockade immunotherapy. Hollow gold nanoshells (HAuNS, a photothermal agent) and AUNP12 (an anti PD-1 peptide, APP) were co-encapsulated into poly­(lactic-co-glycolic) acid (PLGA) nanoparticles. Unlike monoclonal PD-1/PD-L1 antibodies, PD-1 peptide inhibitor shows lower cost and immunotoxicity but needs frequent administration due to its rapid clearance in vivo. Our data here showed that the formed HAuNS- and APP-loaded PLGA nanoparticles (AA@PN) could maintain release periods of up to 40 days for the peptide, and a single intratumoral injection of AA@PN could replace the frequent administration of free APP. After the administration of AA@PN and irradiation with a near-infrared laser at the tumor site, an excellent killing effect on the primary tumor cells was achieved by the PTA. The nanoparticles also played a vaccine-like role under the adjuvant of cytosine-phospho-guanine (CpG) oligodeoxynucleotide and generated a localized antitumor-immune response. Furthermore, sustained APP release with laser-dependent transient triggering could induce the blockage of PD-1/PD-L1 pathway to activate T cells, thus subsequently generating a systemic immune response. Our data demonstrated that the PTA combined with perdurable PD-1 blocking could efficiently eradicate the primary tumors and inhibit the growth of metastatic tumors as well as their formation. The present study provides a promising therapeutic strategy for the treatment of advanced cancer with metastasis and presents a valuable reference for obtaining better outcomes in clinical cancer immunotherapy.
doi_str_mv 10.1021/acsnano.8b00204
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title Laser Immunotherapy in Combination with Perdurable PD‑1 Blocking for the Treatment of Metastatic Tumors
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