Double-camouflaged tellurium nanoparticles for enhanced photothermal immunotherapy of tumor

The photothermal conversion properties of tellurium (Te) nanoparticles have been extensively investigated, rendering them a promising candidate for tumor photothermal therapy. However, there is still room for improvement in the development of efficient Te-based drug delivery systems. Here, Te nanoparticles are mineralized with bioactive molecules within attenuated Salmonella (S-Te), which are subsequently taken up by macrophages (RAW264.7) to construct a double-camouflaged delivery platform (RS-Te). Remarkably, RS-Te retains superior photothermal properties under near-infrared irradiation. The mineralization process eliminates bacterial proliferation potential, thereby mitigating the risk of excessive bacterial growth in vivo. Furthermore, the uptake of bacteria by macrophages not only polarizes them into M1 macrophages to induce an anti-tumor immune response but also circumvents any adverse effects caused by complex antigens on the bacterial surface. The results show that RS-Te can effectively accumulate and retain in tumors. RS-Te-mediated photothermal immunotherapy largely promotes the maturation of dendritic cells and priming of cytotoxic T cells induced by near-infrared laser irradiation. Moreover, RS-Te can switch the activation of macrophages from an immunosuppressive M2 phenotype to a more inflammatory M1 state. The double-camouflaged delivery system may offer highly efficient and safe cancer treatment.

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Publication Details

Journal
Journal of Nanobiotechnology
Published
2024-10-08
DOI
https://doi.org/10.1186/s12951-024-02853-2
Citations
6
Primary Topic
Nanoplatforms for cancer theranostics
Type
article
Field-Weighted Citation Impact
1.11

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article

Double-camouflaged tellurium nanoparticles for enhanced photothermal immunotherapy of tumor

Wei Ni, Bingjie Cai, Chaoqing Li, Jiahao Li et al.
6 citations
Journal of Nanobiotechnology
Nanoplatforms for cancer theranostics
1.11
article

Double-camouflaged tellurium nanoparticles for enhanced photothermal immunotherapy of tumor

Wei Ni, Bingjie Cai, Chaoqing Li, Jiahao Li, Guo‐Jun Zhang, Bin Zhang, Luyao Yang
article en
6 citations

Abstract

The photothermal conversion properties of tellurium (Te) nanoparticles have been extensively investigated, rendering them a promising candidate for tumor photothermal therapy. However, there is still room for improvement in the development of efficient Te-based drug delivery systems. Here, Te nanoparticles are mineralized with bioactive molecules within attenuated Salmonella (S-Te), which are subsequently taken up by macrophages (RAW264.7) to construct a double-camouflaged delivery platform (RS-Te). Remarkably, RS-Te retains superior photothermal properties under near-infrared irradiation. The mineralization process eliminates bacterial proliferation potential, thereby mitigating the risk of excessive bacterial growth in vivo. Furthermore, the uptake of bacteria by macrophages not only polarizes them into M1 macrophages to induce an anti-tumor immune response but also circumvents any adverse effects caused by complex antigens on the bacterial surface. The results show that RS-Te can effectively accumulate and retain in tumors. RS-Te-mediated photothermal immunotherapy largely promotes the maturation of dendritic cells and priming of cytotoxic T cells induced by near-infrared laser irradiation. Moreover, RS-Te can switch the activation of macrophages from an immunosuppressive M2 phenotype to a more inflammatory M1 state. The double-camouflaged delivery system may offer highly efficient and safe cancer treatment.

Journal of NanobiotechnologyVol. 22(1)
Hubei University of Chinese Medicine (CN), Wuhan University (CN), Hubei Provincial Hospital of Traditional Chinese Medicine (CN), Shanghai Zhangjiang Laboratory (CN), Wuhan National Laboratory for Optoelectronics (CN), Renmin Hospital of Wuhan University (CN), Huazhong University of Science and Technology (CN)
China Postdoctoral Science Foundation
Openalex Percentile: Top 24%
Nanoplatforms for cancer theranostics
1.11
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