Covid-19 hyperinflammation and post-Covid-19 illness may be rooted in mast cell activation syndrome

被引:196
|
作者
Afrin, Lawrence B. [1 ]
Weinstock, Leonard B. [2 ]
Molderings, Gerhard J. [3 ]
机构
[1] AIM Ctr Personalized Med, Dept Mast Cell Studies, 3010 Westchester Ave,Suite 404, Purchase, NY 10577 USA
[2] Washington Univ, Dept Med, St Louis, MO USA
[3] Univ Hosp Bonn, Inst Human Genet, Bonn, Germany
关键词
Covid-19; SARS-CoV-2; Mast cell activation syndrome; Mast cell activation disease; Medical hypothesis; TYROSINE KINASE; DISEASE; KIT; PATHOGENESIS;
D O I
10.1016/j.ijid.2020.09.016
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: One-fifth of Covid-19 patients suffer a severe course of Covid-19 infection; however, the specific causes remain unclear. Mast cells (MCs) are activated by SARS-CoV-2. Although only recently recognized, MC activation syndrome (MCAS), usually due to acquired MC clonality, is a chronic multisystem disorder with inflammatory and allergic themes, and an estimated prevalence of 17%. This paper describes a novel conjecture explaining how MCAS might cause a propensity for severe acute Covid-19 infection and chronic post-Covid-19 illnesses. Methods: Observations of Covid-19 illness in patients with/without MCAS were compared with extensive clinical experience with MCAS. Results: The prevalence of MCAS is similar to that of severe cases within the Covid-19-infected population. Much of Covid-19's hyperinflammation is concordant with manners of inflammation which MC activation can drive. Drugs with activity against MCs or their mediators have preliminarily been observed to be helpful in Covid-19 patients. None of the authors' treated MCAS patients with Covid-19 suffered severe infection, let alone mortality. Conclusions: Hyperinflammatory cytokine storms in many severely symptomatic Covid-19 patients may be rooted in an atypical response to SARS-CoV-2 by the dysfunctional MCs of MCAS rather than a normal response by normal MCs. If proven, this theory has significant therapeutic and prognostic implications. (C) 2020 The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.
引用
收藏
页码:327 / 332
页数:6
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