Recent progress and prospects for anti-cytokine therapy in preclinical and clinical acute lung injury

急性呼吸窘迫综合征 医学 临床试验 细胞因子 重症监护医学 细胞激素风暴 生物标志物 免疫学 肺 2019年冠状病毒病(COVID-19) 内科学 疾病 生物 传染病(医学专业) 生物化学
作者
Guilherme Pasetto Fadanni,João Β. Calixto
出处
期刊:Cytokine & Growth Factor Reviews [Elsevier BV]
卷期号:71-72: 13-25 被引量:23
标识
DOI:10.1016/j.cytogfr.2023.07.002
摘要

Acute respiratory distress syndrome (ARDS) is a heterogeneous cause of respiratory failure that has a rapid onset, a high mortality rate, and for which there is no effective pharmacological treatment. Current evidence supports a critical role of excessive inflammation in ARDS, resulting in several cytokines, cytokine receptors, and proteins within their downstream signalling pathways being putative therapeutic targets. However, unsuccessful trials of anti-inflammatory drugs have thus far hindered progress in the field. In recent years, the prospects of precision medicine and therapeutic targeting of cytokines coevolving into effective treatments have gained notoriety. There is an optimistic and growing understanding of ARDS subphenotypes as well as advances in treatment strategies and clinical trial design. Furthermore, large trials of anti-cytokine drugs in patients with COVID-19 have provided an unprecedented amount of information that could pave the way for therapeutic breakthroughs. While current clinical and nonclinical ARDS research suggest relatively limited potential in monotherapy with anti-cytokine drugs, combination therapy has emerged as an appealing strategy and may provide new perspectives on finding safe and effective treatments. Accurate evaluation of these drugs, however, also relies on well-founded experimental research and the implementation of biomarker-guided stratification in future trials. In this review, we provide an overview of anti-cytokine therapy for acute lung injury and ARDS, highlighting the current preclinical and clinical evidence for targeting the main cytokines individually and the therapeutic prospects for combination therapy.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
kygwrw的应助被耕牛热采纳,获得30
刚刚
岁月旧曾谙完成签到,获得积分10
刚刚
完美幻桃完成签到,获得积分10
刚刚
1秒前
七七发布了新的文献求助10
1秒前
大模型的应助被悟空采纳,获得10
1秒前
2秒前
2秒前
wangeil007完成签到,获得积分10
3秒前
lx完成签到,获得积分10
5秒前
深蓝盾狗完成签到,获得积分10
6秒前
7秒前
9秒前
9秒前
11完成签到 ,获得积分10
9秒前
Enigma_GEB举报hgvj的求助涉嫌违规
12秒前
spacetime发布了新的文献求助10
12秒前
12秒前
13秒前
灵巧幻露完成签到,获得积分10
13秒前
手套完成签到,获得积分10
14秒前
14秒前
七七完成签到,获得积分10
14秒前
苏州小北完成签到,获得积分10
15秒前
悟空发布了新的文献求助10
15秒前
asdwind完成签到,获得积分10
16秒前
杰尼龟的鱼完成签到 ,获得积分10
17秒前
17秒前
鞘皮发布了新的文献求助10
18秒前
领导范儿的应助被gogpou采纳,获得10
18秒前
个性的南珍完成签到 ,获得积分10
19秒前
天天快乐的应助被崔尔蓉采纳,获得10
19秒前
21秒前
青山澜发布了新的文献求助10
21秒前
小手冰凉完成签到 ,获得积分10
21秒前
祝你发财完成签到,获得积分10
21秒前
大聪明发布了新的文献求助20
22秒前
linhuafeng完成签到,获得积分10
23秒前
Wang_ZiMo完成签到,获得积分10
23秒前
传奇3的应助被lcj1014采纳,获得10
26秒前
高分求助中
(应助此贴封号)通过应助OA文献获取积分 10000
Rosenblum, Global Change Biology 800
中国器官捐献和移植发展报告(2024) 520
Organizational Behavior 510
Arbitrage Theory in Discrete and Continuous Time 500
Production Logging: Theoretical and Interpretive Elements 400
English Longitudinal Study of Ageing: Waves 0-11, 1998-2024 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 有机化学 化学工程 内科学 物理 生物化学 复合材料 催化作用 细胞生物学 人工智能 心理学 无机化学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 7824233
求助须知:如何正确求助?哪些是违规求助? 9350641
关于积分的说明 20557636
捐赠科研通 7417127
什么是DOI,文献DOI怎么找? 3334391
关于科研通互助平台的介绍 2479727
邀请新用户注册赠送积分活动 2354604