Biomaterials, Journal Year: 2024, Volume and Issue: 316, P. 122998 - 122998
Published: Dec. 9, 2024
Language: Английский
Biomaterials, Journal Year: 2024, Volume and Issue: 316, P. 122998 - 122998
Published: Dec. 9, 2024
Language: Английский
Chemical Society Reviews, Journal Year: 2024, Volume and Issue: 53(12), P. 6399 - 6444
Published: Jan. 1, 2024
This review highlights recent advances in immunological nanomaterials against metastasis and summarizes various nanomaterial-mediated immunotherapy strategies.
Language: Английский
Citations
20Bioengineering & Translational Medicine, Journal Year: 2023, Volume and Issue: 9(1)
Published: Oct. 27, 2023
Abstract Vaccines are an important tool in the rapidly evolving repertoire of immunotherapies oncology. Although cancer vaccines have been investigated for over 30 years, very few achieved meaningful clinical success. However, recent advances areas such antigen identification, formulation development and manufacturing, combination therapy regimens, indication patient selection hold promise to reinvigorate field. Here, we provide a timely update on status vaccines. We identify critically analyze 360 active trials according delivery vehicle, type, indication, other metrics, as well highlight eight globally approved products. Finally, discuss current limitations future applications translation
Language: Английский
Citations
33Advanced Science, Journal Year: 2024, Volume and Issue: 11(15)
Published: Jan. 17, 2024
As an essential intracellular immune activation pathway, the cGAS-STING pathway has attracted broad attention in cancer treatment. However, low bioavailability, nonspecificity, and adverse effects of small molecule STING agonists severely limit their therapeutic efficacy vivo application. In this study, a peptide-based agonist is first proposed, KLA screened out to activate by promoting mitochondrial DNA (mtDNA) leakage. To precisely block PD-1/PD-L1 multi-stimuli activatable peptide nanodrug (MAPN) developed for effective delivery PD-L1 antagonist (CVR). With rational design, MAPN achieved site-specific release CVR response multiple endogenous stimuli, simultaneously activating blocking ultimately initiating robust durable T cell anti-tumor immunity with tumor growth inhibition rate 78% extending median survival time B16F10 tumor-bearing mice 40 days. Overall, antimicrobial peptides, which can promote mtDNA leakage through damaging membranes, may be potential alternatives giving new insight design novel agonists. Furthermore, presents universal platform synergy peptides.
Language: Английский
Citations
13Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: unknown
Published: Oct. 30, 2024
High-entropy nanomaterials (HEMs) are a hot topic in the fields of energy and catalysis. However, terms promising biomedical applications, potential therapeutic studies involving HEMs unprecedented. Herein, we demonstrated high entropy two-dimensional layered double hydroxide (
Language: Английский
Citations
12Cancer Letters, Journal Year: 2025, Volume and Issue: 612, P. 217410 - 217410
Published: Jan. 16, 2025
Language: Английский
Citations
1Advanced Functional Materials, Journal Year: 2024, Volume and Issue: 34(26)
Published: Jan. 9, 2024
Abstract In situ tumor vaccines (ISTVs) hold great potential in immunotherapy, however, three major obstacles, including inadequate endogenous antigen uptake by dendritic cells (DCs), weak T‐cell immune responses, and stubborn immunosuppressive microenvironment (TME), still need to be fully addressed. Herein, a trifecta nanovaccine (TriNV) with TME‐responsive transformable ability is developed tri‐boost antitumor immunity. First, sufficient tumor‐associated antigens (TAAs) are liberated after immunogenic cell death induced via TriNV‐based photoimmunotherapy. the TME, soft‐transformed TriNV improves of TAAs DCs enhance acquired Second, self‐adjuvating released Mn 2+ synergistically promote DC maturation macrophage M1 polarization augmenting stimulator interferon genes activation further amplify responses. Moreover, decomposition MnO 2 within core exhausts glutathione facilitates O release alleviate hypoxia thereby overcoming chemical obstacles TME mitigate immunosuppression. Thus, remarkably eradicates primary tumors inhibits distant metastasis, thus demonstrating as feasible effective ISTV nanoplatform for combating poorly solid tumors.
Language: Английский
Citations
6Bioactive Materials, Journal Year: 2024, Volume and Issue: 42, P. 345 - 365
Published: Sept. 6, 2024
Language: Английский
Citations
5Pharmaceutics, Journal Year: 2023, Volume and Issue: 15(5), P. 1346 - 1346
Published: April 27, 2023
Immunotherapy is among the most effective approaches for treating cancer. One of key aspects successful immunotherapy to achieve a strong and stable antitumor immune response. Modern checkpoint therapy demonstrates that cancer can be defeated. However, it also points out weaknesses immunotherapy, as not all tumors respond co-administration different immunomodulators may severely limited due their systemic toxicity. Nevertheless, there an established way through which increase immunogenicity immunotherapy-by use adjuvants. These enhance response without inducing such severe adverse effects. well-known studied adjuvant strategies improve efficacy metal-based compounds, in more modern implementation-metal-based nanoparticles (MNPs), are exogenous agents act danger signals. Adding innate activation main action immunomodulator makes capable eliciting robust anti-cancer The has peculiarity local administration drug, positively affects its safety. In this review, we will consider MNPs low-toxicity adjuvants could provide abscopal effect when administered locally.
Language: Английский
Citations
11Nano Research, Journal Year: 2024, Volume and Issue: 17(8), P. 7315 - 7336
Published: June 15, 2024
Language: Английский
Citations
4Advanced Materials, Journal Year: 2024, Volume and Issue: unknown
Published: Aug. 28, 2024
Personalized cancer vaccines based on tumor cell lysates offer promise for immunotherapy yet fail to elicit a robust therapeutic effect due the weak immunogenicity of antigens. Autophagosomes, obtained from pleural effusions and ascites patients, have been identified as abundant reservoirs neoantigens that exhibit heightened immunogenicity. However, their potential personalized constrained by suboptimal lymphatic-targeting performances challenges in antigen-presenting endocytosis. Here,a reinforced biomimetic autophagosome-based (BAPs) nanovaccine generated precisely amalgamating autophagosome-derived two types adjuvants capable targeting lymph nodes is developed potently antitumor immunity. The redox-responsive BAPs facilitate cytosolic vaccine opening within cells, thereby exposing antigens stimulate strong immune response. evoke broad-spectrum T-cell responses, culminating effective eradication 71.4% established tumors. Notably, vaccination triggers enduring responses confer protection, with 100% mice shielded against rechallenge significant reduction incidence 87.5%. Furthermore, synergize checkpoint blockade therapy inhibit growth poorly immunogenic breast model. approach presents powerful formula high versatility immunotherapy.
Language: Английский
Citations
4