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

Cytokine Growth Factor Rev. 2023 Jun-Aug:71-72:13-25. doi: 10.1016/j.cytogfr.2023.07.002. Epub 2023 Jul 13.

Abstract

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.

Keywords: ARDS; COVID-19; Combination therapy; Inflammation; Respiratory failure.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Lung Injury* / drug therapy
  • Anti-Inflammatory Agents / therapeutic use
  • Cytokines / therapeutic use
  • Humans
  • Inflammation / drug therapy
  • Respiratory Distress Syndrome* / drug therapy

Substances

  • Anti-Inflammatory Agents
  • Cytokines