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Review
. 2021 Oct;61(10):1274-1285.
doi: 10.1002/jcph.1874. Epub 2021 Jun 12.

Baricitinib: From Rheumatoid Arthritis to COVID-19

Affiliations
Review

Baricitinib: From Rheumatoid Arthritis to COVID-19

Sara Assadiasl et al. J Clin Pharmacol. 2021 Oct.

Abstract

Baricitinib is a JAK1/2 inhibitor that was first approved for treating moderate to severe rheumatoid arthritis (RA) but that later showed considerable efficacy in the control of exaggerated inflammatory responses that occur in a wide range of diseases. There is a growing body of evidence, obtained from clinical trials and case reports, demonstrating clinical and paraclinical improvement in patients following administration of baricitinib including RA, systemic lupus erythematosus, psoriasis, atopic dermatitis, alopecia areata, interferon-mediated autoinflammatory diseases, graft-versus-host disease, diabetic kidney disease, and, recently, coronavirus disease-19. However, despite overall encouraging results, many adverse effects have been observed in baricitinib-treated patients, ranging from simple infections to increased risk of malignancies, particularly in long-term use. The significant efficacy of baricitinib, versus the probable adverse effects, urge further investigation before establishing it as a part of standard therapeutic protocols. Here, we have provided a review of the studies that have used baricitinib for treating various inflammatory disorders and summarized the advantages and disadvantages of its administration.

Keywords: COVID-19; Janus kinase inhibitors; atopic dermatitis; baricitinib; psoriasis; rheumatoid arthritis.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Schematic illustration of JAK/STAT signaling and its inhibition with baricitinib.
Figure 2
Figure 2
Inflammatory conditions treated with baricitinib.

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References

    1. Zhao L, Ma Y, Seemann J, Huang LJ. A regulating role of the JAK2 FERM domain in hyperactivation of JAK2(V617F). Biochem J. 2010;426(1):91‐98. - PMC - PubMed
    1. Schwartz DM, Bonelli M, Gadina M, O'shea JJ. Type I/II cytokines, JAKs, and new strategies for treating autoimmune diseases. Nat Rev Rheumatol. 2016;12(1):25. - PMC - PubMed
    1. Vaddi K, Sarlis NJ, Gupta V. Ruxolitinib, an oral JAK1 and JAK2 inhibitor, in myelofibrosis. Expert Opin Pharmacother. 2012;13(16):2397‐2407. - PubMed
    1. Zerbini CA, Lomonte ABV. Tofacitinib for the treatment of rheumatoid arthritis. Expert Rev Clin Immunol. 2012;8(4):319‐331. - PubMed
    1. Gonzales A, Bowman J, Fici G, Zhang M, Mann D, Mitton‐Fry M. Oclacitinib (APOQUEL®) is a novel Janus kinase inhibitor with activity against cytokines involved in allergy. J Vet Pharmacol Ther. 2014;37(4):317‐324. - PMC - PubMed