COVID-19: Ultrasound-microbubble targeted delivery of immuno-modulatory therapeutics to treat COVID-19
COVID-19:超声微泡靶向递送免疫调节疗法来治疗 COVID-19
基本信息
- 批准号:552687-2020
- 负责人:
- 金额:$ 3.64万
- 依托单位:
- 依托单位国家:加拿大
- 项目类别:Alliance Grants
- 财政年份:2020
- 资助国家:加拿大
- 起止时间:2020-01-01 至 2021-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
COVID-19 caused by the novel coronavirus, SARS-CoV2, is now a historical pandemic due to its ease of transmission, potential to overburden our healthcare systems, and massive disruption to the global economy and everyday life. About 15% of COVID-19 patients require hospitalization and 5% intensive care, ultimately leading to 1-5% of individuals to succumb. The largest source of morbidity and mortality related to COVID-19 is the development of acute respiratory distress syndrome (ARDS) that arises from lung tissue damage and vascular leakage, leading to fluid-filled lungs that make breathing difficult. ARDS is not directly caused by the virus, but rather it is due to an over-reactive immune response known as cytokine release syndrome, or cytokine storm. This is caused by a molecular feedback loop that greatly amplifies inflammation causing general tissue damage. The main culprit for ARDS in COVID-19 seems to be the release of the inflammatory signal interleukin-6 (IL-6) and activation of its receptor (IL-6R). There is significant interest in interrupting IL-6R signaling as a way to abate inflammation and help patients recover. Potential treatments include anti-inflammatory drugs, neutralizing monoclonal antibodies, and RNA therapeutics. However, these drugs are delivered intravenously leading to global reduction of immune function and potential secondary infections. Targeted delivery and release of IL-6R inhibitors in the affected lung tissue would reduce side-effects. Ultrasound and microbubble technologies are emerging as potential workhorses to target the release of and/or stimulate the cellular uptake of therapeutics. Microbubbles are injected into the blood carrying a therapeutic payload, which are released in the presence of ultrasound field aimed at the affected tissue. Here, in collaboration with MD Precision Inc., a company that develops and makes ultrasound devices and applications, we aim to test the use of USMB to deliver silencing RNAs and neutralizing antibodies against IL-6R using cell lines and a mice model of ARDS. If promising, these results will form the basis for USMB applications to treat the worst symptoms of COVID-19, reducing morbidity, mortality, and alleviating pressure on hospitals.
由新型冠状病毒 SARS-CoV2 引起的 COVID-19 由于易于传播、可能使我们的医疗系统负担过重以及对全球经济和日常生活造成巨大破坏,现已成为历史性大流行病。大约 15% 的 COVID-19 患者需要住院治疗,5% 需要重症监护,最终导致 1-5% 的人死亡。与 COVID-19 相关的发病率和死亡率的最大来源是急性呼吸窘迫综合征 (ARDS),该综合征是由肺组织损伤和血管渗漏引起的,导致肺部充满液体,导致呼吸困难。 ARDS 并不是由病毒直接引起的,而是由过度反应的免疫反应(称为细胞因子释放综合征或细胞因子风暴)引起的。 这是由分子反馈回路引起的,该回路极大地放大了导致一般组织损伤的炎症。 COVID-19 中 ARDS 的罪魁祸首似乎是炎症信号白细胞介素 6 (IL-6) 的释放及其受体 (IL-6R) 的激活。人们对中断 IL-6R 信号传导作为减轻炎症和帮助患者康复的一种方式非常感兴趣。潜在的治疗方法包括抗炎药、中和单克隆抗体和 RNA 疗法。然而,这些药物通过静脉注射,导致整体免疫功能下降和潜在的继发感染。在受影响的肺组织中靶向递送和释放 IL-6R 抑制剂将减少副作用。超声波和微泡技术正在成为靶向治疗药物的释放和/或刺激细胞吸收的潜在主力。将携带治疗有效载荷的微泡注入血液中,在针对受影响组织的超声场存在时释放微泡。在这里,我们与 MD Precision Inc.(一家开发和制造超声设备和应用程序的公司)合作,旨在使用细胞系和 ARDS 小鼠模型测试使用 USMB 传递沉默 RNA 和中和抗 IL-6R 抗体。如果有希望,这些结果将成为 USMB 应用的基础,用于治疗 COVID-19 的最严重症状,从而降低发病率、死亡率并减轻医院的压力。
项目成果
期刊论文数量(0)
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Botelho, Roberto其他文献
Aluminum hydroxide adjuvant diverts the uptake and trafficking of genetically detoxified pertussis toxin to lysosomes in macrophages
氢氧化铝佐剂将基因解毒的百日咳毒素转移至巨噬细胞中的溶酶体
- DOI:
10.1111/mmi.14900 - 发表时间:
2022-05 - 期刊:
- 影响因子:3.6
- 作者:
Jaldin-Fincati, Javier;Moussaoui, Serene;Gimenez, Maria Cecilia;Ho, Cheuk Y.;Lancaster, Charlene E.;Botelho, Roberto;Ausar, Fernando;Brookes, Roger;Terebiznik, Mauricio - 通讯作者:
Terebiznik, Mauricio
A Randomized Controlled Trial Comparing BioMime Sirolimus-Eluting Stent With Everolimus-Eluting Stent: Two-Year Outcomes of the meriT-V Trial.
- DOI:
10.14740/cr1498 - 发表时间:
2023-08 - 期刊:
- 影响因子:1.9
- 作者:
Abizaid, Alexandre;Costa, Ricardo;Kedev, Sasko;Kedhi, Elvin;Talwar, Suneel;Erglis, Andrejs;Hlinomaz, Ota;Masotti, Monica;Fath-Ordoubadi, Farzin;Milewski, Krzysztof;Lemos, Pedro;Botelho, Roberto;Ijsselmuiden, Alexander;Koolen, Jacques;Kala, Petr;Janssens, Luc;Chandra, Udita - 通讯作者:
Chandra, Udita
Botelho, Roberto的其他文献
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{{ truncateString('Botelho, Roberto', 18)}}的其他基金
A Dual Camera Acquisition-Spinning Disc Confocal Microscope System to Study Cellular Dynamics
用于研究细胞动力学的双摄像头采集旋转圆盘共焦显微镜系统
- 批准号:
RTI-2023-00091 - 财政年份:2022
- 资助金额:
$ 3.64万 - 项目类别:
Research Tools and Instruments
A Dual Camera Acquisition-Spinning Disc Confocal Microscope System to Study Cellular Dynamics
用于研究细胞动力学的双摄像头采集旋转圆盘共焦显微镜系统
- 批准号:
RTI-2023-00091 - 财政年份:2022
- 资助金额:
$ 3.64万 - 项目类别:
Research Tools and Instruments
Regulation and Function of Phosphoinositide Lipid Signals
磷酸肌醇脂质信号的调节和功能
- 批准号:
RGPIN-2020-04343 - 财政年份:2022
- 资助金额:
$ 3.64万 - 项目类别:
Discovery Grants Program - Individual
Regulation and Function of Phosphoinositide Lipid Signals
磷酸肌醇脂质信号的调节和功能
- 批准号:
RGPIN-2020-04343 - 财政年份:2022
- 资助金额:
$ 3.64万 - 项目类别:
Discovery Grants Program - Individual
Regulation and Function of Phosphoinositide Lipid Signals
磷酸肌醇脂质信号的调节和功能
- 批准号:
RGPIN-2020-04343 - 财政年份:2021
- 资助金额:
$ 3.64万 - 项目类别:
Discovery Grants Program - Individual
Regulation and Function of Phosphoinositide Lipid Signals
磷酸肌醇脂质信号的调节和功能
- 批准号:
RGPIN-2020-04343 - 财政年份:2021
- 资助金额:
$ 3.64万 - 项目类别:
Discovery Grants Program - Individual
Regulation and Function of Phosphoinositide Lipid Signals
磷酸肌醇脂质信号的调节和功能
- 批准号:
RGPIN-2020-04343 - 财政年份:2020
- 资助金额:
$ 3.64万 - 项目类别:
Discovery Grants Program - Individual
Regulation and Function of Phosphoinositide Lipid Signals
磷酸肌醇脂质信号的调节和功能
- 批准号:
RGPIN-2020-04343 - 财政年份:2020
- 资助金额:
$ 3.64万 - 项目类别:
Discovery Grants Program - Individual
Regulation and Function of Phosphoinositide Lipid Signalling
磷酸肌醇脂质信号传导的调节和功能
- 批准号:
RGPIN-2015-06489 - 财政年份:2019
- 资助金额:
$ 3.64万 - 项目类别:
Discovery Grants Program - Individual
Regulation and Function of Phosphoinositide Lipid Signalling
磷酸肌醇脂质信号传导的调节和功能
- 批准号:
RGPIN-2015-06489 - 财政年份:2019
- 资助金额:
$ 3.64万 - 项目类别:
Discovery Grants Program - Individual
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