Digital twin (DT) or so-called ‘building information model (BIM)’ has brought great revolution to the current building industry. Its applications to life cycle management of buildings and infrastructures can further increase the social and economic benefits. As a complete information model, a digital twin integrates the information of a project from different stages of the life cycle into a model, in order to facilitate better asset management and communicate through data visualizations with participants. This paper unprecedently introduces a digital-twin aided life cycle assessment to evaluate a subway station. Dadongmen subway station in Hefei was used as a case study. This new study benchmarks the cost estimation and carbon emission at each life cycle stage of the project. The cost in the construction stage of the project is the highest, accounting for 78% of the total cost. However, the amount of carbon emissions in the operation and maintenance is higher than the amount during the production of building materials, accounting for 67%. Among them, concrete only accounts for 43.66% of the carbon emissions of building materials, even though concrete was mainly used for constructing the metro station. Steel bar and aluminum alloy have carbon emissions of 29.73% and 17.64%, respectively. In addition, emerging risks of the subway stations can be identified. The digital twin has been used to illustrate vulnerability and potential solutions to emerging risks, and to assess the suitability through life cycle cost and carbon footprint. This initiative is relatively new to the industry. The new insight into life cycle assessment or LCA (especially carbon footprint over the life cycle) integrated with digital twin applications will enable sustainable development that will enhance resilience of metro railway systems globally.
Organoids are derived from stem cells or organ-specific progenitors. They display structures and functions consistent with organs in vivo. Multiple types of organoids, including lung organoids, can be generated. Organoids are applied widely in development, disease modelling, regenerative medicine, and other multiple aspects. Various human pulmonary diseases caused by several factors can be induced and lead to different degrees of lung epithelial injury. Epithelial repair involves the participation of multiple cells and signalling pathways. Lung organoids provide an excellent platform to model injury to and repair of lungs. Here, we review the recent methods of cultivating lung organoids, applications of lung organoids in epithelial repair after injury, and understanding the mechanisms of epithelial repair investigated using lung organoids. By using lung organoids, we can discover the regulatory mechanisms related to the repair of lung epithelia. This strategy could provide new insights for more effective management of lung diseases and the development of new drugs.
Cytokines play a crucial role in mediating immune responses to tuberculosis (TB). The aim of this study was to evaluate the levels of cytokines in patients with different forms of pulmonary tuberculosis (PTB) and identify valuable cytokine biomarkers for the diagnosis of PTB. We measured the levels of six cytokines (interleukin (IL-2, IL-4, IL-6, and IL-10), tumor necrosis factor (TNF-α), and interferon-γ (IFN-γ)) in the serum of healthy donors (n = 30). Patients with active PTB (n = 46) and those with latent tuberculosis infection (LTBI, n = 38) were examined using cytometric bead arrays. The levels of the six cytokines in the serum samples were measured promptly, sensitively, and simultaneously. The levels of IL-2, IL-6, IL-10, and IFN-γ were significantly higher in the PTB group compared with those reported in the healthy donors (
P
< 0.01 or
P
< 0.05). In addition, significantly higher levels of IL-2, IL-6, IL-10, and IFN-γ were found in the active PTB group compared with those observed in the LTBI group (
P
< 0.01 or
P
< 0.05). However, the levels of IL-4 and TNF-α in the sera of patients from the PTB group did not show a significant correlation with those measured in the healthy donor group. Our data demonstrated that IL-2, IL-6, IL-10, and IFN-γ may be useful in the auxiliary diagnosis of tuberculosis and as biomarkers for distinguishing LTBI from TB.
Ixodes ticks are the main vectors for a number of zoonotic diseases, including Lyme disease. Ticks secrete saliva directly into a mammalian host while feeding on the host's blood. This action serves to modulate host immunity and coagulation, thus allowing ticks to attach and feed upon their host. One of the most extensively studied components of tick saliva is Salp15. Research has shown that this protein binds specifically to CD4 molecules on the surface of T lymphocytes, interferes with TCR-mediated signaling transduction, inhibits CD4+ T cell activation and proliferation, and impedes the secretion of interleukin 2 (IL-2). Salp15 also binds specifically to dendritic cell dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin (DC-SIGN) to up-regulate the expression of CD73 in regulatory T cells. Collectively, these findings render this salivary protein a potential candidate for a range of therapeutic applications. Here, we discuss our current understanding of Salp15 and the mechanisms that might be used to treat disease.
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