Strong light-matter interactions of exciton in bulk WS2 and a toroidal dipole resonance.

Exciton-polaritonic states are generated by strong interactions between photons and excitons in nanocavities. Bulk transition metal dichalcogenides (TMDCs) host excitons with a large binding energy at room temperature, and thus are regarded as an ideal platform for realizing exciton-polaritons. In this work, we investigate the strong coupling properties between high-Q toroidal dipole (TD) resonance and bulk WS2 excitons in a hybrid metasurface, consisting of Si3N4 nanodisk arrays with embedded WS2. Multipole decomposition and near-field distribution confirm that Si3N4 nanodisk arrays support strong TD resonance. The TD resonance wavelength is easily tuned to overlap with the bulk WS2 exciton wavelength, and strong coupling is observed when the bulk WS2 is integrated with the hollow nanodisk and the oscillator strength of the WS2 material is adjusted to be greater than 0.6. The Rabi splitting of the hybrid device is up to 65 meV. In addition, strong coupling is confirmed by the anticrossing of fluorescence enhancement in the hybrid Si3N4-WS2 metastructure. Our findings are expected to be of importance for both fundamental research in TMDC-based light-matter interactions and practical applications in the design of high-performance exciton-polariton devices.

Active optical modulation of quasi-BICs in Si-VO2 hybrid metasurfaces.

Active optical modulation breaks the limitation of a passive device, providing a new, to the best of our knowledge, alternative to achieve high-performance optical devices. The phase-change material vanadium dioxide (VO2) plays an important role in the active device due to its unique reversible phase transition. In this work, we numerically investigate the optical modulation in resonant Si-VO2 hybrid metasurfaces. The optical bound states in the continuum (BICs) in an Si dimer nanobar metasurface are studied. The quasi-BICs resonator with high quality factor (Q-factor) can be excited by rotating one of the dimer nanobars. The multipole response and near-field distribution confirm that magnetic dipoles dominate this resonance. Moreover, a dynamically tunable optical resonance is achieved by integrating a VO2 thin film to this quasi-BICs Si nanostructure. With the increase of temperature, VO2 gradually changes from the dielectric state to metal state, and the optical response exhibits a significant change. Then, the modulation of the transmission spectrum is calculated. Situations where VO2 is located in different positions are also discussed. A relative transmission modulation of 180% is achieved. These results fully confirm that the VO2 film shows an excellent ability to modulate the quasi-BICs resonator. Our work provides a route for the active modulation of resonant optical devices.

Tunable light trapping in the graphene metasurface.

Graphene metasurfaces based on surface plasmon resonance can greatly enhance the interaction between light and matter at the nanoscale. At present, the resonance of graphene metasurfaces is widely used to enhance the absorption of atomic layer graphene, but little work has focused on the light field trapping capabilities it brings. In this paper, we numerically study the light trapping and manipulation of an asymmetric graphene metasurface. The designed device supports two resonant modes, and the multipole decomposition confirms that the electric dipole response dominates them. The calculated average electric field enhancement factor (EF) can reach 1206 and 1779, respectively. The near-field distribution indicates that the electric field is mainly localized in the graphene nanodisks. When the Fermi energy changes, the intensity and peak position of EF can be effectively regulated. In addition, when the polarization of the incident light is adjusted, the light field capture of the two modes is independently regulated. These results reveal that the graphene metasurface has significant light field capture and regulation ability, which provides a new idea for the realization of active regulation of high-performance low-dimensional optical devices.

Active magnetic dipole emission by the Ge2Sb2Te5 nanodisk.

Active light manipulation plays a critical role in nanophotonics. In this Letter, we investigate the modulation properties of magnetic dipole (MD) emission based on the phase change material Ge2Sb2Te5 hollow nanodisk (GST-HND). The results show that the amorphous GST-HND supports a strong MD response with a radiative decay enhancement of 282 times and quantum efficiency of 100%. More importantly, by tuning the crystallization rate of GST, the active manipulation of MD radiation is achieved with a quantum efficiency modulation depth of up to 95% at a specific wavelength. Our work may provide significant instruction for the active tuning of optical nanodevices.

CD4+ CD8αα+ T cells in the gastric epithelium mediate chronic inflammation induced by Helicobacter felis.

CD4+ CD8αα+ double-positive intraepithelial T lymphocytes (DP T cells), a newly characterized subset of intraepithelial T cells, are reported to contribute to local immunosuppression. However, the presence of DP T cells in Helicobacter. pylori -induced gastritis and their relationship with disease prognosis has yet to be elucidated. In this study, a chronic gastritis model was established by infecting mice with Helicobacter felis. Gastric-infiltrating lymphocytes were isolated from these mice and analyzed by flow cytometry. The frequency of DP T cells in H. felis-induced gastritis mice was higher than that in uninfected mice. The gastric DP T cells were derived from lamina propria cells but were predominantly distributed in the gastric epithelial layer. These gastric DP T cells also exhibited anti-inflammatory functions, and they inhibited the maturation of dendritic cells and proliferation of CD4+ T lymphocytes in vitro. Elimination of DP T cells simultaneously resulted in severe gastritis and a reduction of H. felis load in vivo. Finally, vaccine mixed with different adjuvants was used to explore the relationship between vaccine efficacy and DP cells. Silk fibroin as the vaccine delivery system enhanced vaccine efficacy by reducing the number of DP T cells. This study demonstrated that DP T cells perform an immunosuppressive role in Helicobacter felis-induced gastritis, and consequently, DP T cells may affect disease prognosis and vaccine efficacy.

Helicobacter pylori induces gastric cancer via down-regulating miR-375 to inhibit dendritic cell maturation.

BACKGROUND: Recent studies and clinical samples have demonstrated that Helicobacter pylori could induce the downregulation of miR-375 in the stomach and promote gastric carcinogenesis. However, whether the immune cells are affected by Helicobacter pylori due to the downregulation of miR-375 is unclear. MATERIALS AND METHODS: In this study, we constructed an overexpression and knockdown of miR-375 and Helicobacter pylori infection cell models in vitro. In addition, the maturity of dendritic cells (DCs) and the expression of IL-6, IL-10, and VEGF at the transcriptional and translational levels were analyzed. Changes in the JAK2-STAT3 signaling pathway were detected. In vivo, the number changes in CD4+ T and CD8+ T cells and the size changes of tumors via models of transplantable subcutaneous tumors were also analyzed. RESULTS: A cell model of Helicobacter pylori and gastric cancer was used to identify the expression of miR-375 and the maturity of dendritic cells. This study found that Helicobacter pylori could downregulate miR-375, which regulates the expression of cytokines IL-6, IL-10, and VEGF in the stomach. MiR-375 regulated the expression of cytokines IL-6, IL-10, and VEGF through the JAK2-STAT3 signaling pathway in vitro. In addition, we found that Helicobacter pylori regulates the maturation of dendritic cells through miR-375. These results were further verified in vivo, and miR-375 diminishes tumor size was also demonstrated. This study showed that immature DCs caused a decrease in the number of CD4+ and CD8+ T cells. CONCLUSIONS: This study demonstrated that Helicobacter pylori can inhibit miRNA-375 expression in the stomach. Downregulated miR-375 activates the JAK2-STAT3 pathway. Activating the JAK2-STAT3 signaling pathway promotes the secretion of IL-6, IL-10, and VEGF, leading to immature differentiation of DCs and induction of gastric cancer.

Manipulating Optical Scattering of Quasi-BIC in Dielectric Metasurface with Off-Center Hole.

Bound states in the continuum (BICs) correspond to a particular leaky mode with an infinitely large quality-factor (Q-factor) located within the continuum spectrum. To date, most of the research work reported focuses on the BIC-enhanced light matter interaction due to its extreme near-field confinement. Little attention has been paid to the scattering properties of the BIC mode. In this work, we numerically study the far-field radiation manipulation of BICs by exploring multipole interference. By simply breaking the symmetry of the silicon metasurface, an ideal BIC is converted to a quasi-BIC with a finite Q-factor, which is manifested by the Fano resonance in the transmission spectrum. We found that both the intensity and directionality of the far-field radiation pattern can not only be tuned by the asymmetric parameters but can also experience huge changes around the resonance. Even for the same structure, two quasi-BICs show a different radiation pattern evolution when the asymmetric structure parameter d increases. It can be found that far-field radiation from one BIC evolves from electric-quadrupole-dominant radiation to toroidal-dipole-dominant radiation, whereas the other one shows electric-dipole-like radiation due to the interference of the magnetic dipole and electric quadrupole with the increasing asymmetric parameters. The result may find applications in high-directionality nonlinear optical devices and semiconductor lasers by using a quasi-BIC-based metasurface.

Silk fibroin hydrogel as mucosal vaccine carrier: induction of gastric CD4+TRM cells mediated by inflammatory response induces optimal immune protection against Helicobacter felis.

Tissue-resident memory T (TRM) cells, located in the epithelium of most peripheral tissues, constitute the first-line defense against pathogen infections. Our previous study reported that gastric subserous layer (GSL) vaccination induced a "pool" of protective tissue-resident memory CD4+T (CD4+TRM) cells in the gastric epithelium. However, the mechanistic details how CD4+TRM cells form in the gastric epithelium are unknown. Here, our results suggested that the vaccine containing CCF in combination with Silk fibroin hydrogel (SF) broadened the distribution of gastric intraepithelial CD4+TRM cells. It was revealed that the gastric intraepithelial TRM cells were even more important than circulating memory T cells against infection by Helicobacter felis. It was also shown that gastric-infiltrating neutrophils were involved as indispensable mediators which secreted CXCL10 to chemoattract CXCR3+CD4+T cells into the gastric epithelium. Blocking of CXCR3 or neutrophils significantly decreased the number of gastric intraepithelial CD4+TRM cells due to reduced recruitment of CD4+T cells. This study demonstrated the protective efficacy of gastric CD4+TRM cells against H. felis infection, and highlighted the influence of neutrophils on gastric intraepithelial CD4+TRM cells formation.

Perivascular Lymphocyte Clusters Induced by Gastric Subserous Layer Vaccination Mediate Optimal Immunity against Helicobacter through Facilitating Immune Cell Infiltration and Local Antibody Response.

BACKGROUND: In situ vaccination-induced local inflammatory response resulted in the establishment of a pool of tissue-resident memory T (TRM) cells and new vessels after the resolution of inflammation. TRM cells have received increasing attention; however, the role of new vessels in protective response is still unknown. MATERIALS AND METHODS: We performed the laparotomy to access the stomach and injected alum-based vaccine into the gastric subserous layer (GSL). At 28 days post vaccination, a parabiosis mouse model along with depletion of anti-CD90.2 antibody was employed to explore the function of perivascular lymphocyte clusters in recall responses. The composition of the gastric lymphocyte clusters was analyzed by immunofluorescence staining. Antibody responses were detected using ELISA. Gastric lymphocytes were analyzed using flow cytometry. RESULTS: GSL vaccination induced the formation of new vessels in the inflamed region. These new vessels were different from native vessels in that they were generally accompanied by perivascular lymphocyte clusters that mainly consisted of CD90-expressing cells. Additionally, histological analysis revealed the presence of CD4+ and CD8+ T cells in the perivascular lymphocyte clusters. Administration of a dose of an anti-CD90.2 antibody to GSL-vaccinated mice resolved these clusters. The efficacy of protection was compared in the parabiosis mice. Upon challenge, the presence of perivascular lymphocyte clusters was responsible for the fast recall response, as depletion of these clusters by CD90.2 antibody administration resulted in decreased expressions of VCAM-1, Madcam-1, and TNF-α, as well as lower recruitment of proinflammatory immune cells, decreased antibody levels, and poor protection. CONCLUSIONS: Our research demonstrates that in situ vaccination-induced regional inflammatory response contributes to optimal recall response not only by establishing a CD4+ TRM pool but also by creating an "expressway," i.e., perivascular lymphocyte cluster.

Optical radiation manipulation of Si-Ge2Sb2Te5 hybrid metasurfaces.

Active optical metadevices have attracted growing interest for the use in nanophotonics owing to their flexible control of optics. In this work, by introducing the phase-changing material Ge2Sb2Te5 (GST), which exhibits remarkably different optical properties in different crystalline states, we investigate the active optical radiation manipulation of a resonant silicon metasurface. A designed double-nanodisk array supports a strong toroidal dipole excitation and an obvious electric dipole response. When GST is added, the toroidal response is suppressed, and the toroidal and electric dipoles exhibit pronounced destructive interference owing to the similarity of their far-field radiation patterns. When the crystallization ratio of GST is varied, the optical radiation strength and spectral position of the scattering minimum can be dynamically controlled. Our work provides a route to flexible optical radiation modulation using metasurfaces.

Vaccine-induced gastric CD4+ tissue-resident memory T cells proliferate in situ to amplify immune response against Helicobacter pylori insult.

BACKGROUND: Tissue-resident memory T cells accelerate the clearance of pathogens during recall response. However, whether CD4+ TRM cells themselves can provide gastric immunity is unclear. MATERIALS AND METHODS: We established a parabiosis model between the enhanced green fluorescent protein and wild-type mice that the circulation system was shared, and the wild-type partner was vaccinated with H pylori vaccine composed of CCF and silk fibroin in gastric subserous layer to induce gastric EGFP+ CD4+ TRM cells. Antigen-specific EGFP+ CD4+ T cells and proliferous TRM cells were analyzed by flow cytometry. The colonization of H pylori was detected by quantitative real-time PCR. EGFP+ CD4+ TRM cells and the inflammation of the stomach were observed by histology. RESULTS: A parabiosis animal model was employed to identify the cells that introduced by vaccination in GSL. Antigen-specific EGFP+ CD4+ T cells could be detected at day 7 post-vaccination. Thirty days later, EGFP+ CD4+ TRM cells were established with a phenotype of CD69+ CD103- . Of note, we found that when circulating lymphocytes were depleted by FTY720 administration, these TRM cells could proliferate in situ and differentiate into effector Th1 cells after H pylori challenge. A decrease in H pylori colonization was observed in the vaccinated mice but not unvaccinated mice. Further, we found that although FTY720 was administrated, mounted pro-inflammatory myeloid cells still emerged in the stomach of the vaccinated mice, which might contribute to the reduction of H pylori colonization. CONCLUSIONS: Our study reveals that H pylori vaccine-induced CD4+ TRM cells can proliferate and differentiate in situ to enhance gastric local immunity during recall response.