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Objective: In this study, we investigated the efficacy of percutaneous poking reduction and Kirschner wire fixation in older children with irreducible supracondylar flexion-type fractures of the humerus. Methods: This retrospective investigation included 27 children, comprising 15 males and 12 females, aged between 10 years and 3 months to 14 years and 11 months, all diagnosed with a flexion-type supracondylar fracture of the humerus within one week of trauma. All patients underwent surgery under general anesthesia. Following unsuccessful manual reduction, percutaneous poking reduction with Kirschner wires was performed under C-arm fluoroscopy to achieve fracture reduction. Following successful reduction, three 2.0 mm Kirschner wires were inserted in a cross pattern to secure the fracture ends. Postoperatively, the elbow joint was immobilized in a functional position with a plaster cast for four weeks. Results: Follow-up in the outpatient department ranged from 9 to 36 months. Clinical functional assessment using Flynn's criteria rated 24 cases as excellent, 2 as good, and 1 as fair, yielding an overall efficacy of 96.3%. No cases of fracture re-displacement, fracture fragment necrosis, or other complications such as nonunion, iatrogenic nerve injury, myositis ossificans, or long-term elbow joint dysfunction were observed during the postoperative follow-up. Conclusion: The percutaneous poking reduction and Kirschner wire fixation technique is a simple and reliable procedure for treating irreducible flexion-type supracondylar fractures of the humerus in older children, with minimal trauma. This technique offers substantial stability for the fracture and results in excellent long-term recovery of joint function. [ABSTRACT FROM AUTHOR]

Purpose: Psoriasis is a common cutaneous disease with multiple characteristics including inflammation and aberrant keratinocyte proliferation. However, the pathogenesis of psoriasis is not completely clear yet. The objective of this study is to perform an in-depth analysis of the association between SPRR and LCE in the pathogenesis of psoriasis. Methods: In this study, we explore the differentially expressed genes (DEGs) in psoriasis by analyzing different gene expression profiles obtained from the Gene Expression Omnibus (GEO) database. The DEGs were examined using gene ontology (GO) functional enrichment analysis and protein–protein interactions (PPI) network. Correlation analysis in R studio software was used to analyze the association between SPRR and LCE genes. Further, potential direct protein–protein interactions between SPRR proteins and LCE3D were verified by co-localization observations and co-immunoprecipitation (CO-IP) assays in 293T cells. Also, the expression levels of SPRR and LCE genes were detected in lesional skin of the IMQ-induced psoriasiform dermatitis mice using RT-PCR. Results: Interestingly, the small proline-rich (SPRR) and late cornified envelope (LCE) genes were identified as a module in the constructed PPI network. And the analysis of the gene expression profile GSE63684 showed that both SPRR family and LCE family genes were significantly upregulated in imiquimod (IMQ) induced psoriasiform dermatitis mice. Also, the correlation analysis in R studio software recognized the association of SPRR and LCE genes, which were further verified by co-localization and co-immunoprecipitation (CO-IP) assays in 293T cells, and the results show that the direct interactions between SPRR2 and LCE3D. Notably, we also found that the expression levels of SPRR and LCE genes were significantly increased in the IMQ-induced psoriasiform dermatitis mice, while specifically decreased under the tazarotene cream treatment, indicating that the SPRR and LCEs were regulated simultaneously in psoriasis. Conclusion: In summary, our study found that interactions between SPRR proteins and LCE proteins may provide new insights into the pathogenesis of psoriasis. [ABSTRACT FROM AUTHOR]

Cation disorder in the phosphor lattice could be one of the effective approaches to modify the luminescence efficiency. In this work, cation substitutions of (Mo6+→ V5+) and (Na+→ Mg2+) were conducted in the self-activated NaMg2V3O10. All the samples of Na1+xMg2−xV3−xMoxO10 (x = 0, 0.01, 0.05, 0.1, 0.2, 0.3) were prepared via solid-state reaction. The morphological properties were measured via SEM and EDS analyses. Structural Rietveld refinement was performed to investigate the microstructure in the lattices. The cation substitution brings about structural disorder in the phosphor, which exerts great modifications in the luminescence properties. NaMg2V3O10 presents an intrinsic indirect transition with a band gap of 3.22 eV. The incorporation of Mo6+ and Na+ in the lattices moves the optical absorption to a longer wavelength bringing about a narrower band gap. The luminescence intensity, thermal stability and corresponding lifetime were modified by the cation disorder in the self-activated phosphor. [ABSTRACT FROM AUTHOR]

Purpose: Leukaemia remains a major contributor to global mortality, representing a significant health risk for a substantial number of cancer patients. Despite notable advancements in the field, existing treatments frequently exhibit limited efficacy or recurrence. Here, we explored the potential of abolishing HVEM (herpes virus entry mediator, TNFRSF14) expression in tumours as an effective approach to treat acute lymphoblastic leukaemia (ALL) and prevent its recurrence. Methods: The clinical correlations between HVEM and leukaemia were revealed by public data analysis. HVEM knockout (KO) murine T cell lymphoblastic leukaemia cell line EL4 were generated using CRISPR-Cas9 technology, and syngeneic subcutaneous tumour models were established to investigate the in vivo function of HVEM. Immunohistochemistry (IHC), RNA-seq and flow cytometry were used to analyse the tumour immune microenvironment (TIME) and tumour draining lymph nodes (dLNs). Immune functions were investigated by depletion of immune subsets in vivo and T cell functional assays in vitro. The HVEM mutant EL4 cell lines were constructed to investigate the functional domain responsible for immune escape. Results: According to public databases, HVEM is highly expressed in patients with ALL and acute myeloid leukemia (AML) and is negatively correlated with patient prognosis. Genetic deletion of HVEM in EL4 cells markedly inhibited tumour progression and prolonged the survival of tumour-bearing mice. Our experiments proved that HVEM exerted its immunosuppressive effect by inhibiting antitumour function of CD8+ T cell through CRD1 domain both in vivo and in vitro. Additionally, we identified a combination therapy capable of completely eradicating ALL tumours, which induces immune memory toward tumour protection. Conclusions: Our study reveals the potential mechanisms by which HVEM facilitates ALL progression, and highlights HVEM as a promising target for clinical applications in relapsed ALL therapy. [ABSTRACT FROM AUTHOR]

Aurivillius phase layered perovskites Bi6Ti3WO18 was prepared by the sol-gel citrate-complexation synthesis. The sample developed into the plate-like nanoparticles with the exposed (001) facets. The phase formation and structure have been verified via X-ray polycrystalline powder diffraction (XRD) Rietveld refinements. The nanoparticles were investigated via the measurements such as FE-SEM, TEM, EDS, and the surface analyses. UV–Vis absorption data revealed that the Aurivillius compound has a direct band characteristic with the band energy of 2.214 eV. The band structure of Bi6Ti3WO18 nanoparticles was discussed on the base of the experiments and theoretical calculation. Bi3+-containing Aurivillius Bi6Ti3WO18 shows efficient photocatalytic degradation for rhodamine B dye (RhB) with the visible light irradiation (λ > 420 nm). Dynamic characteristic of the light-created excitons was measured by the luminescence and decay lifetime. The multivalent properties of W and Ti ions in the Aurivillius-like lattices of Bi6Ti3WO18 photocatalyst were discussed. [ABSTRACT FROM AUTHOR]

Cation disorder in the phosphor lattice could be one of the effective approaches to modify the luminescence efficiency. In this work, cation substitutions of (Mo6+→ V5+) and (Na+→ Mg2+) were conducted in the self-activated NaMg2V3O10. All the samples of Na1+xMg2−xV3−xMoxO10 (x = 0, 0.01, 0.05, 0.1, 0.2, 0.3) were prepared via solid-state reaction. The morphological properties were measured via SEM and EDS analyses. Structural Rietveld refinement was performed to investigate the microstructure in the lattices. The cation substitution brings about structural disorder in the phosphor, which exerts great modifications in the luminescence properties. NaMg2V3O10 presents an intrinsic indirect transition with a band gap of 3.22 eV. The incorporation of Mo6+ and Na+ in the lattices moves the optical absorption to a longer wavelength bringing about a narrower band gap. The luminescence intensity, thermal stability and corresponding lifetime were modified by the cation disorder in the self-activated phosphor. [ABSTRACT FROM AUTHOR]