Publications by authors named "Hanqi Zheng"

Multimode responsive optical materials are garnering ever-increasing attention due to their diverse applications. This work showcases a film assembled with rare-earth-doped CaF hollow nanospheres that exhibit water-vapor-triggered dual-mode optical responses. Upon exposure to flowing water vapor, the film rapidly (less than 1.

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  • RNAs are crucial for various biological processes and can interact with other molecules, but current computational methods for identifying these interactions are limited.
  • The study presents a new encoding algorithm designed specifically for RNAs and their interactions, which includes many innovative features and allows for better integration of interacting partners.
  • This algorithm outperforms existing methods in testing and is available for public use on the provided websites.
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Immunogenic cell death (ICD), a dying state of the cells, encompasses the changes in the conformations of cell surface and the release of damage-associated molecular patterns, which could initiate an adaptive immune response by stimulating the dendritic cells to present antigens to T cells. Advancements in biomaterials, nanomedicine, and micro- and nano-technologies have facilitated the development of effective ICD inducers, but the potential toxicity of these vesicles encountered in drug delivery via intravenous administration hampers their further application. As alternatives, the local drug delivery systems have gained emerging attention due to their ability to prolong the retention of high payloads at the lesions, sequester drugs from harsh environments, overcome biological barriers to exert optimal efficacy, and minimize potential side effects to guarantee bio-safety.

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Regulatory T (T) cells underlie multiple autoimmune disorders and potentialize an anti-inflammation treatment with adoptive cell therapy. However, systemic delivery of cellular therapeutics often lacks tissue targeting and accumulation for localized autoimmune diseases. Besides, the instability and plasticity of T cells also induce phenotype transition and functional loss, impeding clinical translation.

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Despite the superior tumor lytic efficacy of oncolytic viruses (OVs), their systemic delivery still faces the challenges of limited circulating periods, poor tumor tropism, and spontaneous antiviral immune responses. Herein, a virus-concealed tumor-targeting strategy enabling OVs' delivery toward lung metastasis via systemic administration is described. The OVs can actively infect, be internalized, and cloak into tumor cells.

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Due to its promising capacity in improving drug efficacy, polypharmacology has emerged to be a new theme in the drug discovery of complex disease. In the process of novel multi-target drugs (MTDs) discovery, in silico strategies come to be quite essential for the advantage of high throughput and low cost. However, current researchers mostly aim at typical closely related target pairs.

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  • Microneedles are being developed for next-gen biosensors due to their minimal invasiveness, high integration, and good biocompatibility, making them ideal for personalized and digital healthcare.
  • The text reviews various designs of microneedle devices, detailing their extraction mechanisms, geometries, and materials, as well as the types of detections they target and their performance.
  • It highlights the shift towards highly integrated sensing systems that use colorimetric, fluorometric, and electronic principles, while also discussing current challenges and future development opportunities in this field.
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  • Tumor vaccination has gained significant attention for its ability to trigger strong immune responses against cancer without the need for identifying specific tumor antigens.
  • Recent innovations involve using bacteria as both targeted delivery systems for vaccines and as effective adjuvants that enhance the immune response.
  • The review highlights various engineering strategies for improving bacteria-based vaccines, such as chemical modification and genetic engineering, while also addressing current challenges and future prospects in this research area.
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Adoptive cell therapy (ACT) that leverages allogeneic or autologous immune cells holds vast promise in targeted cancer therapy. Despite the tremendous success of ACT in treating hematopoietic malignancies, its efficacy is limited in eradicating solid tumors via intravenous infusion of immune cells. With the extending technology of cancer immunotherapy, novel delivery strategies have been explored to improve the therapeutic potency of adoptively transferred cells for solid tumor treatment by innovating the administration route, maintaining the cell viability, and normalizing the tumor microenvironment.

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The dynamic roles of T cells in the immune system to recognize and destroy the infected or mutated cells render T cell therapy a prospective treatment for a variety of diseases including cancer, autoimmune diseases, and allograft rejection. However, the clinical applications of T cell therapy remain unsatisfactory due to the tedious manufacturing process, off-target cytotoxicity, poor cell persistence, and associated adverse effects. To this end, various biomaterials have been introduced to enhance T cell therapy by facilitating proliferation, enhancing local enrichment, prolonging retention, and alleviating side effects.

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  • * Researchers utilized techniques like indirect ELISA, competitive ELISA, and MTT colorimetry to successfully screen the library for positive phage clones.
  • * After three rounds of screening, they found two phage clones that can inhibit the activity of BLyS, indicating successful identification of antagonist peptides.
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Divalent cations, Ca(2 ), Mg(2 ) and Mn(2 ) enhance the binding of bream growth hormone (brGH) to snakehead fish liver membrane, and their optimum concentration was found to be 8 12 mmol/L, at which Ca(2 ), Mg(2 ) and Mn(2 ) could increase, respectively, the specific binding to 230%, 180%, and 200%, compared with the binding in the absence of ions. The Eadie-Scatchard plot was used for the dynamic analysis of the Ca(2 ) binding site. A low affinity Ca(2 ) binding site was found in the GH-receptor complex with K(m)=0.

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