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JAK Inhibitors in Cytokine Storm Syndromes
Camille Keenan1, Sabrin Albeituni1, Kim E Nichols1
1Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA.
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.
Insights
Cytokine storm syndromes (CSSs) are severe hyperinflammatory conditions. Targeting Janus kinases (JAKs) with JAK inhibitors offers a promising therapeutic strategy to reduce inflammation and improve patient outcomes.
Area of Science:
- Immunology
- Pharmacology
- Clinical Medicine
Background:
- Cytokine storm syndromes (CSSs) are life-threatening hyperinflammatory conditions.
- Pro-inflammatory cytokines drive CSSs, often signaling through the Janus kinase (JAK) and signal transducer and activator of transcription (STAT) pathways.
- Some cytokines involved in CSSs are downstream products of JAK/STAT pathway activation.
Purpose of the Study:
- To evaluate the therapeutic potential of targeting JAK/STAT signaling in CSSs.
- To review the efficacy and safety of JAK inhibitors in preclinical and clinical settings for CSSs.
Main Methods:
- Review of preclinical models of CSSs treated with JAK inhibitors.
- Analysis of existing clinical evidence for JAK inhibitor use in CSS patients.
Main Results:
- JAK inhibitors demonstrated efficacy in improving outcomes in preclinical CSS models.
- Clinical evidence suggests JAK inhibition is effective in managing CSSs.
- JAK inhibitors are generally well-tolerated but carry risks, especially with co-existing end-organ dysfunction.
Conclusions:
- Targeting JAK/STAT signaling with JAK inhibitors is a viable therapeutic approach for CSSs.
- Further prospective clinical trials are needed to optimize JAK inhibitor therapy for CSSs, including dosing, scheduling, and combination strategies.
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