
Microbes and Infection, Journal Year: 2023, Volume and Issue: 25(8), P. 105180 - 105180
Published: July 6, 2023
Language: Английский
Microbes and Infection, Journal Year: 2023, Volume and Issue: 25(8), P. 105180 - 105180
Published: July 6, 2023
Language: Английский
Cellular and Molecular Immunology, Journal Year: 2021, Volume and Issue: 18(5), P. 1141 - 1160
Published: April 13, 2021
Abstract The NOD-, LRR-, and pyrin domain-containing protein 3 (NLRP3) inflammasome is a multiprotein complex involved in the release of mature interleukin-1β triggering pyroptosis, which paramount importance variety physiological pathological conditions. Over past decade, considerable advances have been made elucidating molecular mechanisms underlying priming/licensing (Signal 1) assembly 2) NLRP3 activation. Recently, number studies indicated that step regulated by complicated at both transcriptional posttranslational levels. In this review, we discuss current understanding mechanistic details activation with particular emphasis on protein-protein interactions, modifications, spatiotemporal regulation machinery. We also present detailed summary multiple positive and/or negative regulatory pathways providing upstream signals culminate assembly. A better will provide opportunities for development methods prevention treatment inflammasome-related diseases.
Language: Английский
Citations
521Nature Reviews Drug Discovery, Journal Year: 2020, Volume and Issue: 20(1), P. 39 - 63
Published: Oct. 19, 2020
Language: Английский
Citations
336Nature Reviews Rheumatology, Journal Year: 2021, Volume and Issue: 17(7), P. 387 - 404
Published: June 10, 2021
Language: Английский
Citations
226Nature Reviews Rheumatology, Journal Year: 2021, Volume and Issue: 17(10), P. 585 - 595
Published: Aug. 2, 2021
Language: Английский
Citations
172Clinical Rheumatology, Journal Year: 2021, Volume and Issue: 40(7), P. 2611 - 2619
Published: March 17, 2021
Language: Английский
Citations
118Frontiers in Immunology, Journal Year: 2022, Volume and Issue: 13
Published: May 25, 2022
Autoimmune diseases are a group of heterogeneous with diverse clinical manifestations that can be divided into systemic and organ-specific. The common etiology autoimmune is the destruction immune tolerance production autoantibodies, which attack specific tissues and/or organs in body. pathogenesis complicated, genetic, environmental, infectious, even psychological factors work together to cause aberrant innate adaptive responses. Although exact mechanisms unclear, recently, excessive exacerbation pyroptosis, as bond between immunity, has been proven play crucial role development disease. Pyroptosis characterized by pore formation on cell membranes, well rupture excretion intracellular contents pro-inflammatory cytokines, such IL-1β IL-18. This overactive inflammatory programmed death disrupts system homeostasis promotes autoimmunity. review examines molecular structure classical inflammasomes, including NLRP3, AIM2, P2X7-NLRP3, switches their regulation mechanisms. sophisticated pyroptosis pathways, canonical caspase-1-mediated pathway, noncanonical caspase-4/5/11-mediated emerging caspase-3-mediated caspase-independent also described. We highlight recent advances diseases, lupus erythematosus, rheumatoid arthritis, bowel disease, Sjögren’s syndrome dermatomyositis, attempt identify its potential advantages therapeutic target or prognostic marker these diseases.
Language: Английский
Citations
82Frontiers in Immunology, Journal Year: 2023, Volume and Issue: 14
Published: Oct. 4, 2023
Autoimmune diseases (AIDs) are immune disorders whose incidence and prevalence increasing year by year. AIDs produced the system’s misidentification of self-antigens, seemingly caused excessive function, but in fact they result reduced accuracy due to decline system which cannot clearly identify foreign invaders thus issuing false attacks, eventually leading disease. The occurrence is often accompanied emergence inflammation, inflammatory mediators (inflammatory factors, inflammasomes) play an important role pathogenesis AIDs, mediate process affecting innate cells (such as macrophages) adaptive T B cells), ultimately promote autoimmune responses, so targeting mediators/pathways one emerging treatment strategies AIDs. This review will briefly describe inflammation different give a rough introduction inhibitors hoping have reference significance for subsequent options
Language: Английский
Citations
53Journal of Ethnopharmacology, Journal Year: 2023, Volume and Issue: 318, P. 117059 - 117059
Published: Aug. 20, 2023
Language: Английский
Citations
34Clinical and Experimental Medicine, Journal Year: 2024, Volume and Issue: 24(1)
Published: Jan. 29, 2024
Abstract The identification of novel, easily measurable biomarkers inflammation might enhance the diagnosis and management immunological diseases (IDs). We conducted a systematic review meta-analysis to investigate an emerging biomarker derived from full blood count, systemic index (SII), in patients with IDs healthy controls. searched Scopus, PubMed, Web Science inception 12 December 2023 for relevant articles evaluated risk bias certainty evidence using Joanna Briggs Checklist Grades Recommendation, Assessment, Development, Evaluation Working Group system, respectively. In 16 eligible studies, had significantly higher SII when compared controls (standard mean difference, SMD = 1.08, 95% CI 0.75 1.41, p < 0.001; I 2 96.2%, moderate evidence). pooled area under curve (AUC) diagnostic accuracy was 0.85 (95% 0.82–0.88). subgroup analysis, effect size significant across different types ID, barring lupus erythematosus ( 0.20). further analyses, ID active disease vs. those remission (SMD 0.81, 0.34–1.27, 93.6%, AUC 0.74 0.70–0.78). Our study suggests that can effectively discriminate between subjects without disease. Prospective studies are warranted determine whether routine practice. (PROSPERO registration number: CRD42023493142).
Language: Английский
Citations
10Discovery Immunology, Journal Year: 2024, Volume and Issue: 3(1)
Published: Jan. 1, 2024
Fever is a hallmark symptom of disease across the animal kingdom. Yet, despite evidence linking temperature fluctuation and immune response, much remains to be discovered about molecular mechanisms governing these interactions. In patients with rheumatoid arthritis, for instance, it clinically accepted that joint can predict progression. But was only recently demonstrated mitochondria stimulated T cells rise an extreme 50°C, potentially indicating cellular source localized 'fevers'. A challenge dissecting bidirectional interplay between immunity. Heat shock response found in virtually all organisms, activating protective pathways when are exposed elevated temperatures. However, threshold activates vary within same organism, human cells, particular, demonstrating differential sensitivity heat. Such inter-cellular variation may relevant given small but significant differences seen tissues, ages, sexes. Greater understanding how such perturbations mediate responses provide new explanations persistent questions as sex disparity prevalence. Notably, prevalence severity many maladies rising climate change, suggesting fluctuations interact on multiple levels. As global temperatures rising, our body falling, regarding temperature-immune interactions increasingly critical. Here, we review this aspect environmental better understand temperature's role subsequent risk disease.
Language: Английский
Citations
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