Intravenous Anakinra for Macrophage Activation Syndrome May Hold Lessons for Treatment of Cytokine Storm in the Setting of Coronavirus Disease 2019

Macrophage activation syndrome (MAS) and hemophagocytic lymphohistiocytosis (HLH) are increasingly recognized as being on a continuum of cytokine storm syndromes, with different initiating pathways culminating in cytotoxic dysfunction and uncontrolled activation and proliferation of T lymphocytes an...

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Published inACR open rheumatology Vol. 2; no. 5; pp. 283 - 285
Main Author Wampler Muskardin, Theresa L.
Format Journal Article
LanguageEnglish
Published United States John Wiley & Sons, Inc 01.05.2020
John Wiley and Sons Inc
Wiley
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Summary:Macrophage activation syndrome (MAS) and hemophagocytic lymphohistiocytosis (HLH) are increasingly recognized as being on a continuum of cytokine storm syndromes, with different initiating pathways culminating in cytotoxic dysfunction and uncontrolled activation and proliferation of T lymphocytes and macrophages. The activated immune cells produce large amounts of proinflammatory cytokines, including interleukin 1β (IL)‐1β. Management depends on the recognized diagnosis. In the setting of a cytokine storm syndrome and infection, collaborative involvement of specialists, including infectious disease and rheumatology is ideal. Anakinra, a recombinant IL‐1 receptor antagonist, has been used subcutaneously and intravenously in pediatric patients and is considered a first‐line treatment for MAS and secondary HLH (sHLH) among many pediatric rheumatologists. Previous reports of anakinra used in adults for treatment of MAS or sHLH are limited to subcutaneous administration. In this issue, Moneagudo et al. present a series of adult patients with sHLH treated with intravenous anakinra, including patients in whom subcutaneous anakinra was insufficient. As the authors suggest, there is a potential therapeutic use for anakinra in sHLH or the cytokine storm syndrome triggered by COVID19. Trial design will be key, with the patient subpopulation, timing of intervention, and doses tested important.
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Dr. Wampler Muskardin's work is supported by an arthritis research award from the Arthritis National Research Foundation, an NYU‐HHC Clinical and Translational Science Institute KL2 grant, and a Doris Duke Fund to Retain Clinical Scientists award.
Dr. Wampler Muskardin has served on an advisory board for Novartis and as a consultant for Regeneron.
ISSN:2578-5745
2578-5745
DOI:10.1002/acr2.11140