Reply: Calm before the storm: Understanding the role of Janus kinase inhibitors in COVID-19

Abstract

To the Editor: We appreciate the reply by Napolitano et al, “Potential role of Janus kinase inhibitors in COVID-19.”1Napolitano M. Fabbrocini G. Patruno C. Potential role of Janus kinase inhibitors in COVID-19.J Am Acad Dermatol. 2020; 83: e65Abstract Full Text Full Text PDF Scopus (12) Google Scholar Although we agree that there may be a role for Janus kinase (JAK) inhibitors in treating a subset of patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, we respectfully disagree that JAK inhibitors (including baricitinib and upadacitinib) should be continued in all patients taking these medications who develop SARS-CoV-2 infection. There is insufficient evidence to make this recommendation. Napolitano et al1Napolitano M. Fabbrocini G. Patruno C. Potential role of Janus kinase inhibitors in COVID-19.J Am Acad Dermatol. 2020; 83: e65Abstract Full Text Full Text PDF Scopus (12) Google Scholar reference a recent study in which computer modeling suggests that baricitinib might inhibit proteins potentially involved in SARS-CoV-2 entry into cells.2Richardson P. Griffin I. Tucker C. et al.Baricitinib as potential treatment for 2019-nCoV acute respiratory disease.Lancet. 2020; 395: e30-e31Abstract Full Text Full Text PDF PubMed Scopus (905) Google Scholar Not only is that work theoretical, that this potential inhibition might provide clinical benefit to patients infected with SARS-CoV-2 is even further unknown. Also, based on in vitro assays, the concentration of baricitinib needed to inhibit adaptor-associated protein kinase 1 (AAK1) and clathrin-mediated endocytosis would likely require doses far above the United States Food and Drug Administration-approved dose of baricitinib of 2 mg daily.3Stebbing J. Phelan A. Griffin I. et al.COVID-19: combining antiviral and anti-inflammatory treatments.Lancet Infect Dis. 2020; 20: 400-402Abstract Full Text Full Text PDF PubMed Scopus (735) Google Scholar Lastly, the theoretical effect against viral endocytosis only applies to baricitinib; this is not a known property of other JAK inhibitors, including upadacitinib. Based on these considerations, we believe there is insufficient evidence to recommend continuing JAK inhibitors in patients who are acutely infected with SARS-CoV-2. Napolitano et al1Napolitano M. Fabbrocini G. Patruno C. Potential role of Janus kinase inhibitors in COVID-19.J Am Acad Dermatol. 2020; 83: e65Abstract Full Text Full Text PDF Scopus (12) Google Scholar suggest that baricitinib and upadacitinib might be useful in treating the cytokine release syndrome (CRS) that can occur in SARS-CoV-2 infection. We strongly agree that there may be a role for JAK inhibitors in treating SARS-CoV-2–associated CRS. However, it is important to note that this is typically a late manifestation of disease that occurs only in a subset of patients. Furthermore, there is evidence in both rhesus macaques and mice infected with the original SARS virus, SARS-CoV, that a suboptimal early antiviral type I interferon response may predispose to this late manifestation.4Channappanavar R. Fehr A.R. Vijay R. et al.Dysregulated type I interferon and inflammatory monocyte-macrophage responses cause lethal pneumonia in SARS-CoV-infected mice.Cell Host Microbe. 2016; 19: 181-193Abstract Full Text Full Text PDF PubMed Scopus (990) Google Scholar,5Smits S.L. de Lang A. van den Brand J.M.A. et al.Exacerbated innate host response to SARS-CoV in aged non-human primates.PLoS Pathog. 2010; 6: e1000756Crossref PubMed Scopus (264) Google Scholar JAK inhibitors do, however, block the activity of interleukin (IL) 6, a cytokine that is thought to play a central role in SARS-CoV-2–associated CRS. Compared with IL-6 blockade with antibodies (eg, tocilizumab, sarilumab), JAK inhibitors may have an additional advantage of simultaneously blocking other potentially pathogenic cytokines, including IL-2, interferon-γ, granulocyte-macrophage colony-stimulating factor, and granulocyte-colony stimulating factor. Important to note is that the theoretical benefit of JAK inhibitors in this setting is not limited to upadacitinib and baricitinib but also applies to other JAK inhibitors, including ruxolitinib and tofacitinib. We and others are undertaking clinical trials to evaluate JAK inhibitors for SARS-CoV-2–associated CRS, and it will be interesting to see what they show. In summary, we believe there is insufficient evidence to recommend that JAK inhibitors be continued in all patients taking these medications who are acutely infected with SARS-CoV-2. Although JAK inhibitors may prove useful in the treatment of SARS-CoV-2–associated CRS, this is a separate consideration of a relatively uncommon manifestation of this viral infection that occurs late in disease course. Reply: Potential role of Janus kinase inhibitors in COVID-19Journal of the American Academy of DermatologyVol. 83Issue 1PreviewTo the Editor: We read with interest the letter of Peterson et al1 about the use of Janus kinase (JAK) inhibitors in the time of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The authors reported that discontinuation of JAK inhibitors in the setting of the initial infection, such as with SARS-CoV-2, may be beneficial given the role of JAK-signal transducer and activator of transcription (STAT)–dependent type I (α/β) and type II (γ) interferons in antiviral immunity. However, data in the literature regarding the possible use of JAK inhibitors in COVID 19 patients is growing. Full-Text PDF