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

被引:14
作者
Fadanni, Guilherme Pasetto [1 ,2 ]
Calixto, Joao Batista [1 ,2 ,3 ]
机构
[1] Ctr Innovat & Preclin Studies CIENP, Florianopolis, SC, Brazil
[2] Fed Univ Santa Catarina UFSC, Ctr Biol Sci, Dept Pharmacol, Florianopolis, SC, Brazil
[3] Ctr Innovat & Preclin Studies CIEnP, 1302 Ave Luiz Boiteux Piazza, BR-88056000 Florianopolis, SC, Brazil
关键词
ARDS; Inflammation; Combination therapy; COVID-19; Respiratory failure; RESPIRATORY-DISTRESS-SYNDROME; COLONY-STIMULATING FACTOR; NEUTROPHIL RECRUITMENT; INFLAMMATORY CYTOKINES; PERSISTENT ELEVATION; CRITICAL COVID-19; FUSION PROTEIN; INHIBITION; INTERLEUKIN-6; ANTAGONIST;
D O I
10.1016/j.cytogfr.2023.07.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:13 / 25
页数:13
相关论文
共 154 条
[1]   Lenercept (p55 tumor necrosis factor receptor fusion protein) in severe sepsis and early septic shock: A randomized, double-blind, placebo-controlled, multicenter phase III trial with 1,342 patients [J].
Abraham, E ;
Laterre, PF ;
Garbino, J ;
Pingleton, S ;
Butler, T ;
Dugernier, T ;
Margolis, B ;
Kudsk, K ;
Zimmerli, W ;
Anderson, P ;
Reynaert, M ;
Lew, D ;
Lesslauer, W ;
Passe, S ;
Cooper, P ;
Burdeska, A ;
Modi, M ;
Leighton, A ;
Salgo, M ;
Van der Auwera, P .
CRITICAL CARE MEDICINE, 2001, 29 (03) :503-510
[2]   SOCS1 mimetics and antagonists: a complementary approach to positive and negative regulation of immune function [J].
Ahmed, Chulbul M. I. ;
Larkin, Joseph, III ;
Johnson, Howard M. .
FRONTIERS IN IMMUNOLOGY, 2015, 6
[3]   Emapalumab: First Global Approval [J].
Al-Salama, Zaina T. .
DRUGS, 2019, 79 (01) :99-103
[4]   Mechanisms of action of ruxolitinib in murine models of hemophagocytic lymphohistiocytosis [J].
Albeituni, Sabrin ;
Verbist, Katherine C. ;
Tedrick, Paige E. ;
Tillman, Heather ;
Picarsic, Jennifer ;
Bassett, Rachel ;
Nichols, Kim E. .
BLOOD, 2019, 134 (02) :147-159
[5]   The effect of canakinumab on clinical outcomes in patients with COVID-19: A meta-analysis [J].
Ao, Guangyu ;
Wang, Yushu ;
Li, Toni ;
Tran, Carolyn ;
Yang, Qing .
JOURNAL OF INFECTION, 2022, 84 (06) :849-851
[6]   ETOPOSIDE AND CORTICOSTEROID COMBINATION THERAPY IMPROVES ACUTE RESPIRATORY DISTRESS SYNDROME IN MICE [J].
Aoyagi, Tetsuji ;
Sato, Yukio ;
Toyama, Masahiko ;
Oshima, Kengo ;
Kawakami, Kazuyoshi ;
Kaku, Mistuo .
SHOCK, 2019, 52 (01) :83-91
[7]   Role of granulocyte macrophage colony-stimulating factor during gram-negative lung infection with Pseudomonas aeruginosa [J].
Ballinger, Megan N. ;
Paine, Robert, III ;
Serezani, Carlos H. C. ;
Aronoff, David M. ;
Choi, Esther S. ;
Standiford, Theodore J. ;
Toews, Galen B. ;
Moore, Bethany B. .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2006, 34 (06) :766-774
[8]   Granulocyte colony-stimulating factor blockade enables dexamethasone to inhibit lipopolysaccharide-induced murine lung neutrophils [J].
Banuelos, Jesus ;
Cao, Yun ;
Shin, Soon Cheon ;
Bochner, Bruce S. ;
Avila, Pedro ;
Li, Shihong ;
Jiang, Xin ;
Lingen, Mark W. ;
Schleimer, Robert P. ;
Lu, Nick Z. .
PLOS ONE, 2017, 12 (05)
[9]   Selective blockade of interleukin-6 trans-signaling improves survival in a murine polymicrobial sepsis model [J].
Barkhausen, Tanja ;
Tschernig, Thomas ;
Rosenstiel, Philip ;
van Griensven, Martijn ;
Vonberg, Ralf-Peter ;
Dorsch, Martina ;
Mueller-Heine, Annika ;
Chalaris, Athena ;
Scheller, Juergen ;
Rose-John, Stefan ;
Seegert, Dirk ;
Krettek, Christian ;
Waetzig, Georg H. .
CRITICAL CARE MEDICINE, 2011, 39 (06) :1407-1413
[10]   Comparison of systemic cytokine levels in patients with acute respiratory distress syndrome, severe pneumonia, and controls [J].
Bauer, TT ;
Montón, C ;
Torres, A ;
Cabello, H ;
Fillela, X ;
Maldonado, A ;
Nicolás, JM ;
Zavala, E .
THORAX, 2000, 55 (01) :46-52