Journal
POSTGRADUATE MEDICINE
Volume 133, Issue 5, Pages 489-507Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/00325481.2020.1855921
Keywords
SARS-CoV-2; COVID-19; Janus kinase; STAT; inhibitors; cytokine storm; inflammation
Categories
Funding
- Manipal Academy of Higher Education
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As the incidence of COVID-19 increases, efforts are being made to develop therapeutic strategies to combat disease progression, with a focus on the JAK/STAT pathway and its influence on inflammation. Structural and non-structural proteins of SARS-CoV-2 trigger inflammation via this pathway, leading to a cytokine storm in the host. JAK/STAT inhibitors have been employed to reduce excessive inflammation, although their molecular mechanism of action and potential adverse effects require further investigation.
As the incidence of COVID-19 increases with time, more and more efforts are made to pave a way out for the therapeutic strategies to deal with the disease progression. Inflammation being a significant influencer in COVID-19 patients, it drives our focus onto the signaling cascades of the JAK/STAT pathway. JAK phosphorylation mediated by cytokine receptor activation leads to phosphorylation of STATs that translocate into the nucleus to translate for inflammatory mediators. The SARS-CoV-2 structural proteins like spike, nucleocapsid, membrane and envelope proteins along with the non- structural proteins 1-16 including proteases like 3CL (pro) and PLpro promote its entry and survival in hosts. The SARS-CoV-2 infection triggers inflammation via the JAK/STAT pathway leading to recruitment of pneumocytes, endothelial cells, macrophages, monocytes, lymphocytes, natural killer cells and dendritic cells progressing towards cytokine storm. This produces various inflammatory markers in the host that determine the disease severity. The JAK/STAT signaling also mediates immune responses via B cell and T cell differentiation.With an attempt to reduce excessive inflammation, JAK/STAT inhibitors like Ruxolitinib, Baricitinib, Tofacitinib have been employed that mediate its actions via suppressors of cytokine signaling, cytokine inducible SH2 containing protein, Protein inhibitor of activated STAT and protein tyrosine phosphatases. Even though they are implicated with multiple adverse effects, the regulatory authorities have supported its use, and numerous clinical trials are in progress to prove their safety and efficacy. On the contrary, the exact mechanism of JAK/STAT inhibition at molecular levels remains speculative for which further investigations are required.
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