2020
DOI: 10.1016/j.biomaterials.2019.119629
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Modulation of tumor microenvironment using a TLR-7/8 agonist-loaded nanoparticle system that exerts low-temperature hyperthermia and immunotherapy for in situ cancer vaccination

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Cited by 102 publications
(62 citation statements)
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“…At day 14 post-treatment, the representative photographs of excised tumors demonstrated a prominent tumor inhibition effect for C6TI/Apo-Tat NPs upon NIR laser irradiation (Figure 3 c and Figure S24). Nevertheless, this therapeutic efficacy by low-temperature PTT is higher than the reported results, [16] owing to the fact that Apo can efficiently prevent the cytoprotective pathway of the dominant HSP factor, HSP70. [12] Figure 2. a) Normalized UV/Vis/NIR absorption spectra of C6TI in THF and C6TI NPs in PBS.…”
Section: Angewandte Chemiementioning
confidence: 66%
“…At day 14 post-treatment, the representative photographs of excised tumors demonstrated a prominent tumor inhibition effect for C6TI/Apo-Tat NPs upon NIR laser irradiation (Figure 3 c and Figure S24). Nevertheless, this therapeutic efficacy by low-temperature PTT is higher than the reported results, [16] owing to the fact that Apo can efficiently prevent the cytoprotective pathway of the dominant HSP factor, HSP70. [12] Figure 2. a) Normalized UV/Vis/NIR absorption spectra of C6TI in THF and C6TI NPs in PBS.…”
Section: Angewandte Chemiementioning
confidence: 66%
“…[48] These immunoadjuvants can activate TLRrelated signaling pathways,s ubsequently promoting the maturation of DCs,s ecretion of proinflammatory cytokines and chemokines,a nd activation of immune responses.S ung and Chiasg roups reported the use of aR 848-loaded NP (R848@NP) for combinational mild PTT and immunotherapy. [49] TheR848@NP was formed through self-assembly of an amphiphilic polyaniline-glycol-chitosan (PANI-GCS) copolymer synthesized using an oxidative polymerization method, followed by loading of R848 into the hydrophobic core.Inthe tumors after local injection of R848@NP,the temperature was mildly increased via PA NI-mediated PTT upon NIR laser irradiation at 808 nm, resulting in sectional tumor cell death and TAAg eneration. Thes ynergistic action of PTT-induced TAAs and R848 modulated the immunosuppressive tumor microenvironment and induced as trong antitumor immune response.T hus,R 848@NP-mediated combinational PTT and immunotherapy led to complete regression of subcutaneous CT26 tumors and effective suppression of tumor recurrence and metastasis.…”
Section: Combination Of Ptt With Adjuvant Immunotherapymentioning
confidence: 99%
“…Apart from this, PANI was also combined with immunotherapeutic drugs [ 61 ] through hydrophobic interactions to achieve PTT mediated immunotherapy. Overall, the results from these studies reveal that the therapeutic outcome can be enhanced using combinational therapy and necessitating further development of such strategies using PANI.…”
Section: Pani-based Biomaterials For Tumor Ablationmentioning
confidence: 99%