Janus Nanobullets Combine Photodynamic Therapy and Magnetic Hyperthermia to Potentiate Synergetic Anti-Metastatic Immunotherapy.
Zheng WangFan ZhangDan ShaoZhimin ChangLei WangHanze HuXiao ZhengXuezhao LiFangman ChenZhaoxu TuMingqiang LiWen SunLi ChenWen-Fei DongPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2019)
Photodynamic therapy (PDT) is clinically promising in destructing primary tumors but ineffective against distant metastases. This study reports the use of immunogenic nanoparticles mediated combination of PDT and magnetic hyperthermia to synergistically augment the anti-metastatic efficacy of immunotherapy. Janus nanobullets integrating chlorine e6 (Ce6) loaded, disulfide-bridged mesoporous organosilica bodies with magnetic heads (M-MONs@Ce6) are tailored for redox/pH-triggered photosensitizer release accompanying their matrix degradation. Cancer cell membrane cloaking enables favorable tumor-targeted accumulation and prolonged blood circulation time of M-MONs@Ce6. The combination of PDT and magnetic hyperthermia has a strong synergy anticancer activity and simultaneously elicits a sequence of immunogenic cell death, resulting in synergistically tumor-specific immune responses. When combined with anti-CTLA-4 antibody, the biomimetic and biodegradable nanoparticle enables the notable eradication of primary and deeply metastatic tumors with low systematic toxicity, thus potentially advancing the development of combined hyperthermia, PDT, and checkpoint blockade immunotherapy to combat cancer metastasis.
Keyphrases
- photodynamic therapy
- molecularly imprinted
- squamous cell carcinoma
- fluorescence imaging
- papillary thyroid
- cell death
- small cell lung cancer
- immune response
- drug delivery
- squamous cell
- dna damage
- energy transfer
- cell cycle
- oxidative stress
- emergency department
- drinking water
- dendritic cells
- cell proliferation
- young adults
- wound healing
- signaling pathway
- metal organic framework
- pi k akt
- quantum dots