Publications by authors named "Bao Zhong Wang"

Article Synopsis
  • Enhancing immunity in the respiratory tract is vital for fighting influenza through effective mucosal vaccines that can bypass barriers and stimulate immune responses.
  • The study used extracellular vesicles (EVs) as a vaccine platform by attaching influenza hemagglutinin (HA) in an upside-down orientation to expose the conserved parts of the virus.
  • Results showed that intranasal immunization with these EVs led to strong immune responses in mice, providing protection against various influenza strains and highlighting the potential for developing a universal mucosal vaccine.
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  • The initial exposure to influenza viruses creates long-lasting immune memory, affecting responses to future vaccinations and infections.
  • Differences in how earlier infections influence immune responses to various vaccine types were examined in Balb/c mice, showing that closely related strains lead to stronger immunity.
  • Vaccinations following specific past exposures can result in effective protection against related influenza strains and enhance cross-reactive immunity, underscoring the importance of an individual's flu history in vaccine design.
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  • The study highlights the success of mRNA lipid nanoparticle (LNP) vaccines in quickly addressing urgent vaccine needs, but notes their limitations in generating mucosal responses and broad protection against variants.
  • Researchers engineered an advanced mRNA LNP vaccine that includes a novel cytokine adjuvant and influenza A antigen, resulting in strong antibody and T cell responses in mice.
  • Two different adjuvants, GIFT4 and CCL27, were shown to effectively enhance both humoral and cellular immune responses, indicating the potential of cytokine mRNA as a versatile component in mRNA vaccine formulations for improved immunity against viruses.
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Alfalfa ( L.) grassland is prone to degradation following multi-year maintenance. Yet, its mechanism regarding the stoichiometry of carbon (C) and nitrogen (N) across plant-soil system is still unclear.

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Article Synopsis
  • Influenza infections pose a serious threat to global health, prompting the need for improved vaccine formulations due to current vaccines inadequately protecting against circulating strains.
  • Researchers developed a novel intranasal vaccine using protein nanoparticles made of influenza proteins and a bacterial component, which enhanced immune responses in mice.
  • This innovative slow-delivery vaccination method significantly boosted immune responses and survival rates against different strains of the virus, suggesting its potential effectiveness in addressing influenza outbreaks.
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  • The study explores how iron nanostructures, specifically nanoscale zerovalent iron (nZVI), can enhance plant growth, particularly when combined with arbuscular mycorrhizal fungi (AMF).
  • An optimal dosage of 1.0 g·kg of nZVI can boost maize growth significantly, while excessive amounts harm plant roots and disrupt nutrient uptake, unlike FeSO which has minimal effects.
  • The appropriate nZVI facilitates the formation of a supportive nano structure on AMF, improving root colonization, gas exchange, and overall plant health, indicating nZVI plays a crucial role over traditional iron salts.
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  • Enhancing influenza vaccine cross-protection is essential to reduce the public health impact of the virus, with strategies like heterologous sequential immunization showing promise in improving vaccine effectiveness.
  • Research on female Balb/c mice reveals that priming with different vaccine types (mRNA LNP vs. PHC nanoparticles) influences the immune response, with mRNA favoring Th1 responses and PHC promoting Th2 responses.
  • Mucosal immunity is particularly important for cross-protection, with intranasal PHC vaccination outperforming intramuscular methods, and a combination of mRNA prime followed by PHC boost offering the best cross-protection against diverse influenza strains.
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Current influenza vaccine is not effective in providing cross-protection against variants. We evaluated the immunogenicity and efficacy of multi-subtype neuraminidase (NA) and M2 ectodomain virus-like particle (m-cNA-M2e VLP) and chimeric M2e-H3 stalk protein vaccines (M2e-H3 stalk) in ferrets. Our results showed that ferrets with recombinant m-cNA-M2e VLP or M2e-H3 stalk vaccination induced multi-vaccine antigen specific IgG antibodies (M2e, H3 stalk, NA), NA inhibition, antibody-secreting cells, and IFN-γ secreting cell responses.

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Glioblastoma is the most fatal and insidious malignancy, due to the existence of the blood-brain barrier (BBB) and the high invasiveness of tumor cells. Abnormal mitochondrial viscosity has been identified as a key feature of malignancies. Therefore, this study reports on a novel fluorescent probe for mitochondrial viscosity, called ZVGQ, which is based on the twisted intramolecular charge transfer (TICT) effect.

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The conventional inactivated split seasonal influenza vaccine offers low efficacy, particularly in the elderly and against antigenic variants. Here, to improve the efficacy of seasonal vaccination for the elderly population, we tested whether supplementing seasonal bivalent (H1N1 + H3N2) split (S) vaccine with M2 ectodomain repeat and multi-subtype consensus neuraminidase (NA) proteins (N1 NA + N2 NA + flu B NA) on a virus-like particle (NA-M2e) would induce enhanced cross-protection against different influenza viruses in aged mice. Immunization with split vaccine plus NA-M2e (S + NA-M2e) increased vaccine-specific IgG antibodies towards T-helper type 1 responses and hemagglutination inhibition titers.

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Article Synopsis
  • mRNA vaccine technology has seen significant advancements, particularly with the authorization of COVID-19 vaccines, utilizing nano-scale biomaterials as delivery platforms.
  • The impact of these mRNA nanoplatforms on immune responses is still not fully understood, prompting a review of their effects on both innate and adaptive immunity.
  • Additionally, while mRNA vaccines have inherent adjuvant properties, the use of supplemental adjuvants may be necessary to better regulate immune responses.
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In this work, a fluorescent probe, TPABF-HS, was developed for detecting hydrogen sulfide (HS) using a human serum albumin (HSA)-binding-based approach for amplifying the fluorescence signal and extending the linear correlation range. Compared to the most recent probes for HS, the most interesting feature of the detection system developed herein was the especially wide linear range (0-1000 μM (0-100 eq.)), which covered the physiological and pathological levels of HS.

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In this work, we reported a fluorescent probe Fur-SH, a derivative of benzofuranone, which was used to detect HS in living cells and zebrafish. Based on the three structural characteristics of the probe, the effects of different structural modifications on the optical properties of the fluorophore were compared. Then, the fluorophore Fur-OH was synthesized by modifying diethylamino group with benzofuranone as the main skeleton.

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Article Synopsis
  • The first infection with the influenza virus creates a long-lasting immune memory that affects future vaccinations and infections.
  • Researchers developed a PEI-Aichi hemagglutinin (HA)/CpG nanoparticle vaccine that offers cross-protection against different strains of influenza.
  • Mice previously exposed to different HA virus groups exhibited varying antibody responses after vaccination, with those imprinted by group 2 viruses showing stronger protection against subsequent virus challenges compared to group 1.
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Article Synopsis
  • * Mice that received a different vaccine strain (H1N1, H3N2, H5N1, H7N9, H9N2) showed greater immune response and antibody production than those with repeated doses of the same vaccine.
  • * The study emphasized the importance of both antibody and T cell immunity in achieving broader protection against various influenza strains with a heterologous vaccination strategy.
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Article Synopsis
  • Influenza epidemics pose significant risks to public health and the economy, prompting the need for better vaccines against respiratory infections.
  • A new protein nanoparticle is developed using influenza nucleoprotein at its core, coated with specific fusion proteins, which enhances immune response when paired with adjuvants like ISCOMs and MPLA.
  • Tests show that these adjuvanted nanoparticles induce strong immune responses, resulting in higher antibody levels and strong memory cell populations in mice, achieving a 100% survival rate against viral challenges.
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We investigated the priming effect of nanoscale zero-valent iron (nZVI) on carbon sink and iron uptake, and the possible mediation by AMF (arbuscular mycorrhizal fungi, Funneliformis mosseae) in semiarid agricultural soils. Maize seed dressings comprised of three nZVI concentrations of 0, 1, 2 g·kg and was tested with and without AMF inoculation under high and low soil moistures, respectively. The ICP-OES observations indicated that both low dose of nZVI (1 g·kg) and high dose of nZVI (2 g·kg) significantly increased the iron concentrations in roots (L: 54.

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Article Synopsis
  • Scientists looked at a nature-based solution that used a special layer of tiny plants (biocrust) mixed with alfalfa and maize crops to help save carbon in very damaged soils.
  • They found that using this method greatly reduced soil erosion by nearly 95% and helped keep carbon and nitrogen in the soil too, while also helping to catch and store rainwater better.
  • Overall, the biocrust helped plants grow better and improved the tiny life in the soil, leading to healthier soil and more carbon storage compared to regular farming methods.
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  • mRNA vaccines have shown effectiveness and safety in preventing infectious diseases, prompting the development of a novel multivalent influenza vaccine using lipid nanoparticles (LNPs) encoding various viral proteins.
  • Immunization with these mRNA LNPs led to strong immune responses, promoting both cellular immunity and high levels of specific antibodies in mice, especially when cGAMP was used as an adjuvant.
  • The addition of cGAMP resulted in significantly enhanced immune responses, including increased secretion of important cytokines and a greater presence of memory T cells in both the spleen and lungs, ultimately providing strong protection against different strains of the virus.
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An improved method for the generation of peptide vaccines using di-tyrosine cross-linking is described. The conserved ion channel peptide, M2e, of influenza A virus was modified with the addition of small tyrosine-rich regions (GYGY-) at both the N- and C-termini and extensively cross-linked via tyrosine-tyrosine linkages to form peptide nanoclusters. The cross-linking was catalyzed using exogenous nickel(II) ions complexed to an exogenous glycine-glycine-histidine peptide in the presence of an oxidizer.

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Rhizosphere effect of nanoscale zero-valent iron (nZVI) is crucial but little reported. Maize seeds were dressed with four nZVI concentrations (0, 1.0, 1.

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Influenza virus hemagglutinin (HA) stem is currently regarded as an extremely promising immunogen for designing universal influenza vaccines. The appropriate antigen-presenting vaccine vector would be conducive to increasing the immunogenicity of the HA stem antigen. In this study, we generated chimeric virus-like particles (cVLPs) co-displaying the truncated C-terminal of DnaK from and H1 stem or full-length H1 antigen using the baculovirus expression system.

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Article Synopsis
  • Universal influenza vaccines are critical for preventing future outbreaks and pandemics, prompting the creation of double-layered protein nanoparticles that contain two key influenza antigens.
  • The nanoparticles stimulate immune responses by encouraging cytokine release from immune cells and generating strong antibody and T cell responses.
  • The addition of MPLA, an immune booster, enhances the vaccine's effectiveness and reduces inflammation in the lungs after influenza infection.
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Adjuvants can increase the magnitude and durability of the immune response generated by the vaccine antigen. Aluminum salts (Alum) remain the main adjuvant licensed for human use. A few new adjuvants have been licensed for use in human vaccines since the 1990s.

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