Search

Rare‐earth permanent magnet synchronous machines face challenges in manipulating their magnetic fields, which hinders the ability to extend the operation speed range. Moreover, this inflexibility leads to reduced efficiency in high‐speed scenarios when the machine is under flux‐weakening control and increases the risk of the magnets becoming demagnetised. The authors propose an alterable‐magnetic‐circuit variable‐flux memory machine (AMC‐VFMM) and a multi‐objective hierarchical optimisation method is conducted to optimise the machine. Firstly, the topology and alterable‐magnetic‐circuit principle of the proposed AMC‐VFMM are introduced. Then, optimisation objectives including torque production capability, flux regulation capability, and resisting unintentional demagnetisation capability are defined, and the hierarchical optimisation approach is established by stratifying the optimisation objectives and variables through the sensitivity analysis. Finite element analysis indicates that electromagnetic performances of the optimised design scheme are significantly enhanced. The bench test of the prototype demonstrates the superiority of the proposed AMC‐VFMM and validates the effectiveness of the optimisation design method. [ABSTRACT FROM AUTHOR]

Neutrophil extracellular trap (NET) is one of the defense functions of neutrophils, which has a rapid ability to kill infections and is also crucial in a variety of immune‐associated diseases including infections, tumors and autoimmune diseases. Recent studies have shown that NETs are closely related to the development of tumors. The regulatory role of NETs in tumors has been of interest to researchers. In addition to awakening latent tumor cells, NETs can also promote the proliferation and development of tumor cells and their metastasis to other sites. At the same time, NETs also have the effect of inhibiting tumors. At present, there are some new advances in the impact of NETs on tumor development, which will provide a more theoretical basis for developing NET‐targeted drugs. Therefore, this review just summarized the formation process of NETs, the regulation of tumor development and the treatment methods based on NETs. [ABSTRACT FROM AUTHOR]

Follicular T helper (Tfh) cells are a subset of CD4+ T cells that play an important role in the formation of germinal centers and the maturation and differentiation of affinity‐matured B cells. Recent studies have demonstrated important functions of Tfh cells in tertiary lymphoid structures of tumors, revealing great potential of Tfh cells in tumor immunity. However, Tfh development is incompletely understood. The differentiation of Tfh cells is a complex, multistage process regulated at the DNA, RNA and protein levels. This review just summarizes current research on the molecular mechanisms of Tfh cell differentiation to better understand the role of Tfh cells in antitumor immunity. [ABSTRACT FROM AUTHOR]

Follicular regulatory T (Tfr) cells are a novel and unique subset of effector regulatory T (Treg) cells that are located in germinal centers (GCs). Tfr cells express transcription profiles that are characteristic of both follicular helper T (Tfh) cells and Treg cells and negatively regulate GC reactions, including Tfh cell activation and cytokine production, class switch recombination and B cell activation. Evidence also shows that Tfr cells have specific characteristics in different local immune microenvironments. This review focuses on the regulation of Tfr cell differentiation and function in unique local immune microenvironments, including the intestine and tumor. [ABSTRACT FROM AUTHOR]

Follicular helper T (TFH) cells are essential for inducing germinal centre (GC) reactions to mediate humoral adaptive immunity and antiviral effects, but the mechanisms of TFH cell differentiation remain unclear. Here, we found that the hippo kinase MST1 is critical for TFH cell differentiation, GC formation, and antibody production under steady‐state conditions and viral infection. MST1 deficiency intrinsically enhanced TFH cell differentiation and GC reactions in vivo and in vitro. Mechanistically, mTOR and HIF1α signalling is involved in glucose metabolism and increased glycolysis and decreased OXPHOS, which are critically required for MST1 deficiency‐directed TFH cell differentiation. Moreover, upregulated Foxo3 expression is critically responsible for TFH cell differentiation induced by Mst1−/−. Thus, our findings identify a previously unrecognized relationship between hippo kinase MST1 signalling and mTOR‐HIF1α‐metabolic reprogramming coupled with Foxo3 signalling in reprogramming TFH cell differentiation. [ABSTRACT FROM AUTHOR]

CD8+ T cells play a crucial role in anti‐tumour immunity, but they often undergo exhaustion, which affects the anti‐tumour activity of CD8+ T cells. The effect and mechanism of exhausted CD8+ T cells have become the focus of anti‐tumour immunity research. Recently, a large number of studies have confirmed that long‐term antigen exposure can induce exhaustion. Cytokines previously have identified their effects (such as IL‐2 and IL‐10) may play a dual role in the exhaustion process of CD8+ T cells, suggesting a new mechanism of inducing exhaustion. This review just focuses our current understanding of the biology of exhausted CD8+ T cells, including differentiation pathways, cellular characteristics and signalling pathways involved in inducing exhaustion, and summarizes how these can be applied to tumour immunotherapy. [ABSTRACT FROM AUTHOR]

Intestinal macrophages are the most abundant immune cells in the small and large intestine, which maintain intestinal homeostasis by clearing invading bacteria and dead cells, secreting anti‐inflammatory cytokines, and inducing tolerance to symbiotic bacteria and food particles. In addition, as antigen‐presenting cells, they also participate in eliciting adaptive immune responses through bridging innate immune responses. After the intestinal homeostasis is disrupted, the damaged or apoptotic intestinal epithelial cells cannot be effectively cleared, and the infection of exogenous pathogens and leakage of endogenous antigens lead to persistent intestinal inflammation. Long‐term chronic inflammation is one of the important causes of colitis‐associated carcinogenesis (CAC). Tumor microenvironment (TME) is gradually formed around tumor cells, in which tumor associated macrophage (TAMs) is not only the builder, but also regulated by TME. This review just briefly summarized the role of intestinal macrophages under physiological and pathological inflammatory and cancerous conditions, and current therapeutic strategies for intestinal diseases targeting macrophages. [ABSTRACT FROM AUTHOR]

Selenium, as one of the essential microelements, plays an irreplaceable role in metabolism regulation and cell survival. Selenium metabolism and regulation have great effects on physiological systems especially the immune system. Therefore, selenium is tightly related to various diseases like cancer. Although recent research works have revealed much about selenium metabolism, the ways in which selenium regulates immune cells' functions and immune‐associated diseases still remain much unclear. In this review, we will briefly introduce the regulatory role of selenium metabolism in immune cells and immune‐associated diseases. [ABSTRACT FROM AUTHOR]

N6‐methyladenosine (m6A) RNA methylation is a reversible posttranscriptional modification in eukaryotes involving three types of functional proteins: "writers", "erasers", and "readers". m6A regulates the metabolism of messenger RNAs and noncoding RNAs through RNA structure, splicing, stability, export, and translation, thereby participating in various physiological and pathological processes. Here, we summarize the current state of m6A methylation researches, focusing on how these modifications modulate the fate decisions of innate and adaptive immune cells and regulate immune responses in immune‐associated diseases, including viral infections and cancer. These studies showed that m6A modifications and m6A modifying proteins play a critical role in pathogen recognition, immune cell activation, immune cell fate decisions, and immune reactions. m6A is a novel regulator of immune system homeostasis and activation. [ABSTRACT FROM AUTHOR]