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JAK Inhibitors in Cytokine Storm Syndromes

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Date 2024 Aug 8
PMID 39117841
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Abstract

Cytokine storm syndromes (CSSs) comprise a group of severe and often fatal hyperinflammatory conditions driven by the overproduction of pro-inflammatory cytokines by activated cells of the immune system. Many of the CSS-associated cytokines mediate their downstream effects by signaling through the Janus kinases (JAKs) and signal transducers and activators of transcription (STATs). In addition, several of these cytokines are produced downstream of JAK/STAT pathway activation. Therefore, targeting JAK/STAT signaling using small molecule JAK inhibitors has become an increasingly appealing therapeutic option to dampen hyperinflammation in patients with CSSs. Application of JAK inhibitors in preclinical CSS models has shown improvements in multiple sequelae of hyperinflammation, and there is growing clinical evidence supporting the efficacy of JAK inhibition in patients with these conditions. Although generally well tolerated, JAK inhibitor use is not without potential for toxicity, especially in settings like CSSs where end-organ dysfunction is common. More prospective clinical trials incorporating JAK inhibitors, alone or in combination with other immunomodulatory therapies, are necessary to determine the optimal dosing, schedule, efficacy, and tolerability of these agents for patients experiencing CSSs.

References
1.
Ghoreschi K, Laurence A, OShea J . Janus kinases in immune cell signaling. Immunol Rev. 2009; 228(1):273-87. PMC: 2782696. DOI: 10.1111/j.1600-065X.2008.00754.x. View

2.
Schulert G, Canna S . Convergent pathways of the hyperferritinemic syndromes. Int Immunol. 2018; 30(5):195-203. PMC: 7189979. DOI: 10.1093/intimm/dxy012. View

3.
McLornan D, Pope J, Gotlib J, Harrison C . Current and future status of JAK inhibitors. Lancet. 2021; 398(10302):803-816. DOI: 10.1016/S0140-6736(21)00438-4. View

4.
Schwartz D, Kanno Y, Villarino A, Ward M, Gadina M, OShea J . JAK inhibition as a therapeutic strategy for immune and inflammatory diseases. Nat Rev Drug Discov. 2017; 17(1):78. PMC: 6168198. DOI: 10.1038/nrd.2017.267. View

5.
Verstovsek S, Mesa R, Gotlib J, Levy R, Gupta V, Dipersio J . A double-blind, placebo-controlled trial of ruxolitinib for myelofibrosis. N Engl J Med. 2012; 366(9):799-807. PMC: 4822164. DOI: 10.1056/NEJMoa1110557. View