Adaptation of the living therapeutic materials concept to the immune sensing of neutrophil granulocytes.

IF 3.6 3区 医学 Q3 CELL BIOLOGY
Islam Mohamed, Kristin Burckhardt, Stefan Lohse
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引用次数: 0

Abstract

Neutrophils are innate immune cells that perpetually patrol the circulation and tissues. They sense and migrate toward invading microbes to initiate and orchestrate a robust immune response. Their highly reactive nature, driven by multiple and redundant receptor families recognizing bacterial components, makes them particularly sensitive to contaminants or nonsterile implants. This often leads to a neutrophil-driven foreign body reaction that shields the implant and triggers inflammation, collateral tissue damage, or even sepsis. This presents a significant challenge for living therapeutic materials, an innovative biomedical approach using genetically engineered bacteria encapsulated in natural or synthetic polymers. Since bacterial turnover inevitably releases pathogen-associated molecular patterns that activate neutrophils to mitigate or prevent a potent neutrophil response, living therapeutic material design strategies are required to protect the living therapeutic material from damage while maintaining its functionality. This review focuses on current strategies involving bacterial genetic engineering, immune-shielding materials and factors, and modified hydrogel-based systems to minimize immune recognition. Engineering the bacterial chassis to produce immune tolerance-inducing metabolites from commensals, modified pathogen-associated molecular patterns, and pathogen-associated molecular pattern-cleaving autolysins may enhance biocompatibility. A crucial aspect for clinical translation is robust biocontainment to prevent bacterial escape, ensuring living therapeutic material remains a safe and effective therapeutic platform. While the potential of the living therapeutic material concept lies in the development of tailored medicine specifically designed for a specific disease and enabling local, cost-effective, site- and stimulus-responsive treatment, balancing the neutrophil immune response remains an important milestone on the path to living therapeutic material for future biomedical applications.

活体治疗材料概念对中性粒细胞免疫感知的适应。
中性粒细胞是天生的免疫细胞,它永远在循环和组织中巡逻。它们感知并向入侵的微生物迁移,以启动和协调一种强大的免疫反应。它们的高度反应性,由识别细菌成分的多个和冗余受体家族驱动,使它们对污染物或非无菌植入物特别敏感。这通常会导致中性粒细胞驱动的异物反应,保护植入物并引发炎症、附带组织损伤,甚至败血症。这对生物治疗材料提出了重大挑战,这是一种创新的生物医学方法,将基因工程细菌封装在天然或合成聚合物中。由于细菌周转不可避免地释放病原体相关的分子模式,激活中性粒细胞以减轻或阻止有效的中性粒细胞反应,因此需要设计活性治疗材料的策略来保护活性治疗材料免受损害,同时保持其功能。本文综述了目前的一些策略,包括细菌基因工程、免疫屏蔽材料和因子以及改良的水凝胶系统,以最大限度地减少免疫识别。改造细菌底盘,从共生体、修饰病原体相关分子模式和病原体相关分子模式切割自溶蛋白中产生诱导免疫耐受的代谢物,可能会增强生物相容性。临床翻译的一个关键方面是强大的生物控制,以防止细菌逃逸,确保活的治疗材料仍然是一个安全有效的治疗平台。虽然活体治疗材料概念的潜力在于开发专门针对特定疾病设计的量身定制药物,并实现局部,成本效益,部位和刺激反应治疗,但平衡中性粒细胞免疫反应仍然是未来生物医学应用活体治疗材料道路上的重要里程碑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Leukocyte Biology
Journal of Leukocyte Biology 医学-免疫学
CiteScore
11.50
自引率
0.00%
发文量
358
审稿时长
2 months
期刊介绍: JLB is a peer-reviewed, academic journal published by the Society for Leukocyte Biology for its members and the community of immunobiologists. The journal publishes papers devoted to the exploration of the cellular and molecular biology of granulocytes, mononuclear phagocytes, lymphocytes, NK cells, and other cells involved in host physiology and defense/resistance against disease. Since all cells in the body can directly or indirectly contribute to the maintenance of the integrity of the organism and restoration of homeostasis through repair, JLB also considers articles involving epithelial, endothelial, fibroblastic, neural, and other somatic cell types participating in host defense. Studies covering pathophysiology, cell development, differentiation and trafficking; fundamental, translational and clinical immunology, inflammation, extracellular mediators and effector molecules; receptors, signal transduction and genes are considered relevant. Research articles and reviews that provide a novel understanding in any of these fields are given priority as well as technical advances related to leukocyte research methods.
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