Understanding the link between bone marrow failure and chronic inflammation through the lens of VEXAS syndrome
从 VEXAS 综合征的角度了解骨髓衰竭与慢性炎症之间的联系
基本信息
- 批准号:MR/Y011945/1
- 负责人:
- 金额:$ 106.67万
- 依托单位:
- 依托单位国家:英国
- 项目类别:Research Grant
- 财政年份:2024
- 资助国家:英国
- 起止时间:2024 至 无数据
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
As we age, the bone marrow becomes less effective in producing cells within the blood and the immune system. In part, this is due to changes that occur with age in the genetic make-up of bone marrow cells. Despite these genetic changes not uniformly driving a robust and homogenous disease phenotype, the functional alterations in various immune cells lead to systemic effects on blood cell production and the ability of the immune system to respond to challenges. As a result, individuals can become less able to fight infection and more likely to produce damaging levels of inflammation in a process frequently referred to as "inflammageing". Although inflammageing has been linked to many chronic diseases, we do not fully understand exactly how specific genetic changes in the bone marrow are linked to inflammation. This is where the study of conditions such as VEXAS syndrome (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) is critical. This syndrome is a newly discovered disorder in which affected individuals can suffer bone marrow failure and severe inflammation in the context of a specific change in the genetic code of blood stem cells and their immune cell progeny. In the majority of cases, the genetic mutation occurs in UBA1, a molecule that controls several important cell functions including inflammation. Because of this clear link between a specific genetic change, bone marrow failure and inflammation, we can use VEXAS syndrome to understand these relationships in more detail and develop new laboratory tests to track disease evolution and identify therapeutic options. The knowledge we will gain by studying VEXAS syndrome will help improve our overall understanding of inflammageing and how this process contributes to the development of other common chronic age-related disorders.
随着年龄的增长,骨髓在血液和免疫系统中产生细胞的效率会降低。在某种程度上,这是由于骨髓细胞的基因组成随着年龄的增长而发生的变化。尽管这些基因变化并不能统一驱动强大且同质的疾病表型,但各种免疫细胞的功能改变会对血细胞生成和免疫系统应对挑战的能力产生系统性影响。结果,个体抵抗感染的能力变得较差,并且更有可能在通常被称为“炎症”的过程中产生破坏性的炎症水平。尽管炎症与许多慢性疾病有关,但我们并不完全了解骨髓中的特定基因变化如何与炎症相关。这就是 VEXAS 综合征(空泡、E1 酶、X 连锁、自身炎症、体细胞)等疾病的研究至关重要的地方。这种综合征是一种新发现的疾病,在血液干细胞及其免疫细胞后代的遗传密码发生特定变化的情况下,受影响的个体可能会遭受骨髓衰竭和严重炎症。在大多数情况下,基因突变发生在 UBA1 中,UBA1 是一种控制包括炎症在内的多种重要细胞功能的分子。由于特定基因变化、骨髓衰竭和炎症之间存在明显的联系,我们可以使用 VEXAS 综合征来更详细地了解这些关系,并开发新的实验室测试来跟踪疾病演变并确定治疗方案。通过研究 VEXAS 综合征,我们将获得的知识将有助于提高我们对炎症的整体理解,以及该过程如何促进其他常见慢性与年龄相关疾病的发展。
项目成果
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Sinisa Savic其他文献
Chlorhexidine allergy in four specialist allergy centres in the United Kingdom, 2009–13: clinical features and diagnostic tests
2009-13 年英国四个专科过敏中心的洗必太过敏:临床特征和诊断测试
- DOI:
10.1111/cei.12944 - 发表时间:
2017-02-14 - 期刊:
- 影响因子:4.6
- 作者:
William Egner;Matthew Helbert;R. Sargur;K. Swallow;N. Harper;T. Garcez;Sinisa Savic;L. Savic;Eren Effren - 通讯作者:
Eren Effren
The Ca 2+ sensor STIM1 regulates type I interferon response by retaining the signaling adaptor STING at the endoplasmic reticulum
Ca 2 传感器 STIM1 通过在内质网保留信号适配器 STING 来调节 I 型干扰素反应
- DOI:
- 发表时间:
2024-09-14 - 期刊:
- 影响因子:0
- 作者:
Sonal Srikanth;Jin Seok Woo;Beibei Wu;Y. M. El;Jennifer;Leung;Koollawat Chupradit;Laura Rice;G. Seo;Guillaume Calmettes;C. Ramakrishna;Edouard Cantin;Dong Sung An;Ren Sun;Ting;Wu;Jae U. Jung;Sinisa Savic;Y. Gwack - 通讯作者:
Y. Gwack
Sugammadex: the sting in the tail?
Sugammadex:尾巴被刺痛?
- DOI:
10.1016/j.bja.2018.07.014 - 发表时间:
2018-10-01 - 期刊:
- 影响因子:9.8
- 作者:
L. Savic;Sinisa Savic;Philip M. Hopkins;Philip M. Hopkins - 通讯作者:
Philip M. Hopkins
Oral Sebetralstat for On-Demand Treatment of Hereditary Angioedema Attacks.
口服 Sebetralstat 用于按需治疗遗传性血管性水肿发作。
- DOI:
10.1056/nejmoa2314192 - 发表时间:
2024-05-31 - 期刊:
- 影响因子:158.5
- 作者:
Marc A. Riedl;Henriette Farkas;E. Aygören‐Pürsün;Fotis Psarros;D. Soteres;Maria Staevska;Mauro Cancian;David Hagin;Daisuke Honda;Isaac Melamed;Sinisa Savic;Marcin Stobiecki;Paula J Busse;Eunice Dias de Castro;Nancy Agmon;R. Gower;Aharon Kessel;Marcin Kurowski;Ramon Lleonart;Vesna Grivcheva Panovska;H. Wedner;Paul K Audhya;J. Hao;Matthew Iverson;Michael D. Smith;Christopher M Yea;W. Lumry;A. Zanichelli;Jonathan A Bernstein;Marcus Maurer;D. M. Cohn - 通讯作者:
D. M. Cohn
Sinisa Savic的其他文献
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