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Synthetically rewired macrophages to foster tissue regeneration post virus induced lung damage

Synthetically rewired macrophages to foster tissue regeneration post virus induced lung damage
合成重组巨噬细胞促进病毒引起的肺损伤后组织再生
批准号:
524821872
负责人:
Professor Dr. Nico Lachmann
金额:
$0.0万
依托单位国家:
德国
项目类别:
Research Grants
财政年份:
--
资助国家:
德国
项目状态:
未结题
起止时间:

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中文摘要
翻译
有针对性地支持身体自身的功能代表了一种新的、有吸引力的对抗疾病的策略(称为:宿主定向治疗,HDT)。HDT的一个重点是减少加重的炎症和平衡病理部位的免疫反应性。除其他疾病外,肺部的细菌和病毒感染与严重的组织损伤有关,有助于感染相关的致死率并促进微生物生态位。为了支持组织再生,以细胞为基础的巨噬细胞免疫疗法是特别感兴趣的,因为这些细胞(i)本质上提供组织再生和体内平衡的功能,(ii)迁移到受损组织,(iii)感知组织环境的信号,并可以诱导促炎或抗炎反应。在这个创新项目中,我们的目标是开发一种基于巨噬细胞的HDT策略,该策略可以干扰病原体诱导的超炎症并减少加剧的组织损伤。利用合成生物学,基因修饰的传感器/效应巨噬细胞将被开发出来,它们自主地将内源性感染相关信号转化为可靠的反应,最终导致组织再生。该策略将在免疫功能小鼠肺部感染的小鼠传感器/效应巨噬细胞和在先进的体外系统以及人源化小鼠中的人类传感器/效应巨噬细胞中进行评估。
英文摘要
The targeted support of the body's own functions represents a new, attractive strategy for combating disease (referred to as: host-directed therapy, HDT). One focus of HDT is to reduce exacerbated inflammation and to balance immune reactivity at sites of pathology. Among other diseases, bacterial and viral infections of the lung are associated with severe tissue damage, contributing to infection associated lethality and promoting microbial niches. To support tissue regeneration, cell-based immunotherapies with macrophages are of particular interest, as these cells (i) intrinsically provide functions for tissue regeneration and homeostasis, (ii) migrate to damaged tissue and (iii) sense the signals of the tissue environment and can induce pro- or anti-inflammatory responses. In this innovative project we aim to develop a macrophage based HDT strategy that perturbs pathogen-induced hyper-inflammation and reduces exacerbated tissue damage. Using synthetic biology, genetically modified sensor/effector macrophages will be developed that autonomously convert endogenous, infection-associated signals into reliable responses that ultimately lead to tissue regeneration. This strategy will be evaluated for mouse sensor/effector macrophages in the context of pulmonary infection in immunocompetent mice and for human sensor/effector macrophages in advanced in vitro systems as well as in humanized mice.
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