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Optical bound states in continuum (BICs) are the special lossless electromagnetic resonance modes found in optical transmission media. Optical BICs supported by metasurfaces can bring a series of image-based applications, which can be classified into far-field image-based applications and near-field image-based applications according to imaging distance. The far field image-based applications of optical BICs supported by metasurfaces have been proved theoretically and experimentally. However, the near-field image-based applications are still in the stage of theoretical demonstration, and its practical feasibility is still questioned. In this letter, we have experimentally demonstrated the feasibility of near-field image-based applications of optical BICs. An all-silicon terahertz metasurface that supports near-field displaying based on quasi-BIC is designed. Its unit cell is based on the classic asymmetric elliptical strip structure, and one unit cell of the metasurface corresponds to one display pixel. By observing the electric field distribution of the metasurface in the near-field region, the display of the given image is successfully constructed. The near-field image-based application of BICs may be beneficial for the information encryption, the hidden item detection, matter analysis, etc.
RESUMO
Quasi-bound states in the continuum (q-BICs) in optical metasurfaces have been found to carry special radiation polarization properties. Herein, we have studied the relationship between the radiation polarization state of a q-BIC and the polarization state of the output wave, and theoretically proposed a perfect linear polarization wave generator controlled by the q-BIC. The proposed q-BIC has an x-polarized radiation state, and the y co-polarized output wave is completely eliminated by introducing additional resonance at the q-BIC frequency. Finally, a perfect x-polarized transmission wave with very low background scattering is obtained, and the transmission polarization state is not limited by the incident polarization state. The device can be used to efficiently obtain narrowband linearly polarized waves from non-polarized waves, and can also be used for polarization-sensitive high-performance spatial filtering.
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The appearance of all-dielectric micro-nano photonic devices constructed from high refractive index dielectric materials offers a low-loss platform for the manipulation of electromagnetic waves. The manipulation of electromagnetic waves by all-dielectric metasurfaces reveals unprecedented potential, such as focusing electromagnetic waves and generating structured light. Recent advances in dielectric metasurfaces are associated with bound states in the continuum, which can be described as non-radiative eigen modes above the light cone supported by metasurfaces. Here, we propose an all-dielectric metasurface composed of elliptic cross pillars arranged periodically and verify that the displacement distance of a single elliptic pillar can control the strength of the light-matter interaction. Specifically, when the elliptic cross pillar is C4 symmetric, the quality factor of the metasurface at the Γ point is infinite, also called the bound states in the continuum. Once the C4 symmetry is broken by moving a single elliptic pillar, the corresponding metasurface engenders mode leakage; however, the large quality factor still exists, which is called the quasi-bound states in the continuum. Then, it is verified by simulation that the designed metasurface is sensitive to the refractive index change of the surrounding medium, indicating that it can be applied for refractive index sensing. Moreover, combined with the specific frequency and the refractive index variation of the medium around the metasurface, the information encryption transmission can be realized effectively. Therefore, we envisage that the designed all-dielectric elliptic cross metasurface can promote the development of miniaturized photon sensors and information encoders due to its sensitivity.
RESUMO
PURPOSE: Non-melanoma skin cancers of the face are at high-risk for local recurrence and metastatic spread. While surgical interventions such as Mohs microsurgery are considered the standard of care, this modality has the potential for high rates of toxicity in sensitive areas of the face. Catheter flap high-dose-rate (HDR) brachytherapy has shown promising results, with high rates of local control and acceptable cosmetic outcomes. MATERIAL AND METHODS: Patients with non-melanoma skin cancers (NMSC) located on the face were treated with 40 Gy in 8 fractions, given twice weekly via catheter flap HDR brachytherapy. Clinical target volume (CTV) included the visible tumor plus a margin of 5 mm in all directions, with no additional planning target volume (PTV) margin. RESULTS: Fifty patients with 53 lesions on the face were included, with a median follow-up of 15 months. All were considered high-risk based on NCCN guidelines. Median tumor size and thickness were 18 mm and 5 mm, respectively. Median PTV volume and D90 were 1.7 cc and 92%, respectively. Estimated rate of local control at twelve months was 92%. Three patients (5%) experienced acute grade 2 toxicity. Two patients (4%) continued to suffer from chronic grade 1 skin toxicity at 12 months post-radiotherapy (RT), with an additional two patients (4%) experiencing chronic grade 2 skin toxicity. Forty-nine lesions (92%) were found to have a good or excellent cosmetic outcome with complete tumor remission. CONCLUSIONS: CT-based flap applicator brachytherapy is a valid treatment option for patients with NMSC of the face. This modality offers high rates of local control with acceptable cosmetic outcomes and low rates of toxicity.
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The generation of tumour-specific T cells is critically important for cancer immunotherapy. A major challenge in achieving a robust T-cell response is the spatiotemporal orchestration of antigen cross-presentation in antigen-presenting cells with innate stimulation. Here, we report a minimalist nanovaccine, comprising a simple physical mixture of an antigen and a synthetic polymeric nanoparticle, PC7A NP, which generates a strong cytotoxic T-cell response with low systemic cytokine expression. Mechanistically, the PC7A NP achieves efficient cytosolic delivery of tumour antigens to antigen-presenting cells in draining lymph nodes, leading to increased surface presentation while simultaneously activating type I interferon-stimulated genes. This effect is dependent on stimulator of interferon genes (STING), but not the Toll-like receptor or the mitochondrial antiviral-signalling protein (MAVS) pathway. The nanovaccine led to potent tumour growth inhibition in melanoma, colon cancer and human papilloma virus-E6/E7 tumour models. The combination of the PC7A nanovaccine and an anti-PD-1 antibody showed great synergy, with 100% survival over 60 days in a TC-1 tumour model. Rechallenging of these tumour-free animals with TC-1 cells led to complete inhibition of tumour growth, suggesting the generation of long-term antitumour memory. The STING-activating nanovaccine offers a simple, safe and robust strategy in boosting anti-tumour immunity for cancer immunotherapy.
Assuntos
Linfócitos T CD8-Positivos/imunologia , Vacinas Anticâncer , Imunidade Celular/efeitos dos fármacos , Proteínas de Membrana , Nanopartículas , Neoplasias Experimentais/terapia , Proteínas Adaptadoras de Transdução de Sinal/imunologia , Animais , Linfócitos T CD8-Positivos/patologia , Vacinas Anticâncer/química , Vacinas Anticâncer/imunologia , Vacinas Anticâncer/farmacologia , Humanos , Imunoterapia , Proteínas de Membrana/química , Proteínas de Membrana/imunologia , Proteínas de Membrana/farmacologia , Camundongos , Camundongos Knockout , Nanopartículas/química , Nanopartículas/uso terapêutico , Proteínas de Neoplasias/imunologia , Neoplasias Experimentais/imunologia , Neoplasias Experimentais/patologia , Células THP-1RESUMO
Activation of the DNA-dependent cytosolic surveillance pathway in response to Mycobacterium tuberculosis infection stimulates ubiquitin-dependent autophagy and inflammatory cytokine production, and plays an important role in host defense against M. tuberculosis. However, the identity of the host sensor for M. tuberculosis DNA is unknown. Here we show that M. tuberculosis activated cyclic guanosine monophosphate-adenosine monophosphate (cGAMP) synthase (cGAS) in macrophages to produce cGAMP, a second messenger that activates the adaptor protein stimulator of interferon genes (STING) to induce type I interferons and other cytokines. cGAS localized with M. tuberculosis in mouse and human cells and in human tuberculosis lesions. Knockdown or knockout of cGAS in human or mouse macrophages blocked cytokine production and induction of autophagy. Mice deficient in cGAS were more susceptible to lethality caused by infection with M. tuberculosis. These results demonstrate that cGAS is a vital innate immune sensor of M. tuberculosis infection.