Drug-induced mast cell eradication: A novel approach to treat mast cell activation disorders?

被引:19
|
作者
Valent, Peter [1 ,2 ]
Akin, Cem [3 ]
Hartmann, Karin [4 ,5 ,6 ]
Reiter, Andreas [7 ]
Gotlib, Jason [8 ]
Sotlar, Karl [9 ]
Sperr, Wolfgang R. [1 ,2 ]
Degenfeld-Schonburg, Lina [1 ,2 ]
Smiljkovic, Dubravka [1 ,2 ]
Triggiani, Massimo [10 ]
Horny, Hans-Peter [11 ]
Arock, Michel [12 ]
Galli, Stephen J. [13 ,14 ]
Metcalfe, Dean D. [15 ]
机构
[1] Med Univ Vienna, Dept Internal Med 1, Div Hematol & Hemostaseol, Waehringer Guertel 18-20, A-1090 Vienna, Austria
[2] Med Univ Vienna, Ludwig Boltzmann Inst Hematol & Oncol, Waehringer Guertel 18-20, A-1090 Vienna, Austria
[3] Univ Michigan, Div Allergy & Clin Immunol, Ann Arbor, MI USA
[4] Univ Hosp Basel, Dept Dermatol, Div Allergy, Basel, Switzerland
[5] Univ Basel, Basel, Switzerland
[6] Univ Hosp Basel, Dept Biomed, Basel, Switzerland
[7] Univ Hosp Mannheim, Dept Hematol & Oncol, Mannheim, Germany
[8] Stanford Univ, Sch Med, Stanford Canc Inst, Stanford, CA USA
[9] Paracelsus Med Univ Salzburg, Inst Pathol, Salzburg, Austria
[10] Univ Salerno, Div Allergy & Clin Immunol, Salerno, Italy
[11] Ludwig Maximilians Univ Munchen, Inst Pathol, Munich, Germany
[12] Sorbonne Univ, Pitie Salpetriere Charles Foix Hosp, AP HP, Dept Hematol Biol, Paris, France
[13] Stanford Univ, Sch Med, Dept Pathol, Dept Microbiol & Immunol, Stanford, CA USA
[14] Stanford Univ, Sch Med, Sean N Parker Ctr Allergy & Asthma Res, Stanford, CA USA
[15] NIAID, Mast Cell Biol Sect, Lab Allerg Dis, NH, 9000 Rockville Pike, Bethesda, MD 20892 USA
基金
奥地利科学基金会;
关键词
Mast cells; KIT; Mast cell activation syndrome; tyrosine kinase inhibitor; midostaurin; avapritinib; TYROSINE KINASE INHIBITOR; FACTOR KIT-LIGAND; SYSTEMIC MASTOCYTOSIS; C-KIT; BONE-MARROW; MEDIATOR RELEASE; DEPENDENT ACTIVATION; IMATINIB MESYLATE; I EXPRESSION; STEM-CELLS;
D O I
10.1016/j.jaci.2022.04.003
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Mast cell (MC) activation is a key event in allergic reactions, other inflammatory states, and MC activation syndromes. MC-stabilizing agents, mediator-targeting drugs, and drugs interfering with mediator effects are often prescribed for these patients. However, the clinical efficacy of these drugs varies depending on the numbers of involved MCs and the underlying pathology. One straightforward approach would be to eradicate the primary target cell. To date however, no MC-eradicating treatment approach has been developed for patients with MC activation disorders. Nevertheless, recent data suggest that long-term treatment with agents effectively inhibiting KIT function results in the virtual eradication of tissue MCs and a sustained decrease in serum tryptase levels. In many of these patients, MC depletion is associated with a substantial improvement in mediator-induced symptoms. In patients with an underlying KIT D816V-positive mastocytosis, such MC eradication requires an effective inhibitor of KIT D816V, such as avapritinib. However, the use of KIT inhibitors must be balanced against their potential side effects. Here we discuss MC-eradicating strategies in various disease models, the feasibility of this approach, available clinical data, and future prospects for the use of KIT-targeting drugs in MC activation disorders.
引用
收藏
页码:1866 / 1874
页数:9
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