Targeting immunomodulation following cardiac injury
心脏损伤后靶向免疫调节
基本信息
- 批准号:MR/T017074/1
- 负责人:
- 金额:$ 227.36万
- 依托单位:
- 依托单位国家:英国
- 项目类别:Research Grant
- 财政年份:2020
- 资助国家:英国
- 起止时间:2020 至 无数据
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
Cardiovascular diseases cause more than a quarter of all deaths in the UK, (approximately 170,000 deaths each year - an average of 460 deaths each day or one every three minutes). Of these, coronary heart disease is the most common and is the leading cause of heart attack. Heart attack manifests as massive death of muscle cells, upwards of around one billion, accounting for around 25% loss of the total heart muscle. There is no means to replace these lost cells and consequently the injury is patched-up by the formation of a non-contractile, scar to prevent rupture of the wall of the heart. This, in turn, increases the burden on survived muscle and results in increased cell size, wall thinning, dilation of the chambers and ultimately progression to heart failure. Currently there are around 900,000 people living in the UK with heart failure; organ transplantation is the only current long-term solution, but is complicated by immune rejection and the fact that demand continually outstrips the availability of donor hearts. Alternative regenerative approaches have centred on the replacement of lost cells generated from a variety of sources (bone marrow, fat tissue and skeletal muscle), however, these have largely failed, with disappointing clinical trial results. One reason for this is that the local environment of the injured heart becomes highly inflamed and scarred due to the invasion of immune cells which in turn leads to further cell death and failure to support the integration of new cells into survived tissue. Elsewhere in the body immune cells are cleared to draining lymph nodes by lymphatic vessels after injury (for eg. following skin excision injury). We recently discovered that the lymphatics of the heart respond to injury in mice by sprouting and further identified that these expanding vessels function to clear immune cells which, when increased by growth factor treatment, improved the outcome after a heart attack. In this proposal, we seek to determine whether timed stimulation of the growth of cardiac lymphatics can define the optimal window for intervention after injury and which types of immune cells are best retained in the heart versus cleared lymph nodes to optimise heart repair and function after a heart attack. Correlating timed clearance of precisely defined immune cells with outcome, will enable us to uniquely attribute function to different subsets of immune cells as an important insight. We will also model human lymphatic vessels and their interactions with immune cells and screen these models for drug compounds which might activate the lymphatics. This will represent the first stage of a drug-discovery pipeline targeting the local environment, to enable cell repopulation and tissue restoration, as part of a combined therapy to treat heart attack patients.
在英国,心血管疾病占所有死亡人数的四分之一以上(每年约 170,000 人死亡 - 平均每天 460 人死亡,即每三分钟 1 人死亡)。其中,冠心病是最常见的,也是心脏病发作的主要原因。心脏病发作表现为肌肉细胞大量死亡,数量超过十亿,约占心肌总量的 25%。没有办法替换这些丢失的细胞,因此,损伤可以通过形成非收缩性疤痕来修补,以防止心壁破裂。这反过来又增加了存活肌肉的负担,导致细胞大小增加、壁变薄、心室扩张,最终进展为心力衰竭。目前英国约有 90 万人患有心力衰竭;器官移植是目前唯一的长期解决方案,但由于免疫排斥反应以及供体心脏供不应求的事实,使情况变得复杂。替代的再生方法集中于替换各种来源(骨髓、脂肪组织和骨骼肌)产生的丢失细胞,然而,这些方法基本上都失败了,临床试验结果令人失望。原因之一是,由于免疫细胞的入侵,受伤心脏的局部环境变得高度炎症和疤痕,进而导致细胞进一步死亡,并且无法支持新细胞整合到存活的组织中。在身体的其他部位,受伤后(例如皮肤切除损伤后),免疫细胞会被淋巴管清除到引流淋巴结。我们最近发现,小鼠心脏的淋巴管通过发芽来应对损伤,并进一步发现这些扩张的血管具有清除免疫细胞的功能,当通过生长因子治疗增加免疫细胞时,可以改善心脏病发作后的结果。在本提案中,我们试图确定对心脏淋巴管生长的定时刺激是否可以定义损伤后干预的最佳窗口,以及哪些类型的免疫细胞与清除的淋巴结相比最能保留在心脏中,以优化心脏病发作后的心脏修复和功能。将精确定义的免疫细胞的定时清除与结果相关联,将使我们能够将功能独特地归因于不同免疫细胞子集,作为重要的见解。我们还将模拟人类淋巴管及其与免疫细胞的相互作用,并在这些模型中筛选可能激活淋巴管的药物化合物。这将代表针对当地环境的药物发现管道的第一阶段,以实现细胞再生和组织恢复,作为治疗心脏病患者的联合疗法的一部分。
项目成果
期刊论文数量(6)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Angiogenesis - Methods and Protocols
血管生成 - 方法和方案
- DOI:10.1007/978-1-0716-2059-5_13
- 发表时间:2022
- 期刊:
- 影响因子:0
- 作者:Klaourakis K
- 通讯作者:Klaourakis K
Immune cells in cardiac repair and regeneration.
- DOI:10.1242/dev.199906
- 发表时间:2022-04-15
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
The evolving cardiac lymphatic vasculature in development, repair and regeneration.
- DOI:10.1038/s41569-020-00489-x
- 发表时间:2021-05
- 期刊:
- 影响因子:0
- 作者:Klaourakis K;Vieira JM;Riley PR
- 通讯作者:Riley PR
Tissue-resident macrophages regulate lymphatic vessel growth and patterning in the developing heart.
- DOI:10.1242/dev.194563
- 发表时间:2021-02-03
- 期刊:
- 影响因子:0
- 作者:Cahill TJ;Sun X;Ravaud C;Villa Del Campo C;Klaourakis K;Lupu IE;Lord AM;Browne C;Jacobsen SEW;Greaves DR;Jackson DG;Cowley SA;James W;Choudhury RP;Vieira JM;Riley PR
- 通讯作者:Riley PR
Lymphatic Clearance of Immune Cells in Cardiovascular Disease.
心血管疾病中免疫细胞的淋巴清除率。
- DOI:10.3390/cells10102594
- 发表时间:2021-09-29
- 期刊:
- 影响因子:6
- 作者:Ravaud C;Ved N;Jackson DG;Vieira JM;Riley PR
- 通讯作者:Riley PR
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Paul Riley其他文献
SYSTEMATIC ASSESSMENT OF THE EFFECT OF DIRECT ORAL ANTICOAGULANTS DABIGATRAN, RIVAROXABAN AND APIXABAN USING CALIBRATED AUTOMATED THROMBIN GENERATION ASSAY IN VIVO
- DOI:
10.1016/s0735-1097(16)30769-0 - 发表时间:
2016-04-05 - 期刊:
- 影响因子:
- 作者:
Ramin Artang;Maren Anderson;Paul Riley;Joern Dalsgaard Nielsen - 通讯作者:
Joern Dalsgaard Nielsen
Perspectives on long-term medical management of urea cycle disorders: insights from a survey of UK healthcare professionals
- DOI:
10.1186/s13023-025-03647-x - 发表时间:
2025-03-19 - 期刊:
- 影响因子:3.500
- 作者:
Karolina M. Stepien;Melanie McSweeney;Antonio Ochoa-Ferraro;Roshni Vara;Paul Riley;Megan Smith - 通讯作者:
Megan Smith
Paul Riley的其他文献
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{{ truncateString('Paul Riley', 18)}}的其他基金
IDRM Spatial Transcriptomics Platform
IDRM 空间转录组学平台
- 批准号:
BB/W019612/1 - 财政年份:2022
- 资助金额:
$ 227.36万 - 项目类别:
Research Grant
Investigating the role of macrophage-deposited collagen in the injured mouse heart
研究巨噬细胞沉积的胶原蛋白在受伤小鼠心脏中的作用
- 批准号:
MR/V038095/1 - 财政年份:2021
- 资助金额:
$ 227.36万 - 项目类别:
Research Grant
Investigating Thymosin beta4-mediated myocardial regeneration and anti-inflammatory wound healing in the injured heart
研究胸腺素β4介导的心肌再生和抗炎伤口愈合的受损心脏
- 批准号:
G0701970/1 - 财政年份:2008
- 资助金额:
$ 227.36万 - 项目类别:
Research Grant
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