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Drug-induced mast cell eradication: A novel approach to treat mast cell activation disorders?
Valent, Peter; Akin, Cem; Hartmann, Karin; Reiter, Andreas; Gotlib, Jason; Sotlar, Karl; Sperr, Wolfgang R; Degenfeld-Schonburg, Lina; Smiljkovic, Dubravka; Triggiani, Massimo; Horny, Hans-Peter; Arock, Michel; Galli, Stephen J; Metcalfe, Dean D.
Affiliation
  • Valent P; Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria; Ludwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria. Electronic address: peter.valent@meduniwien.ac.at.
  • Akin C; Division of Allergy and Clinical Immunology, University of Michigan, Ann Arbor, Mich.
  • Hartmann K; Division of Allergy, Department of Dermatology, University Hospital Basel and University of Basel, Switzerland; Department of Biomedicine, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Reiter A; Department of Hematology and Oncology, University Hospital Mannheim, Mannheim, Germany.
  • Gotlib J; Stanford Cancer Institute/Stanford University School of Medicine/Stanford Cancer Institute, Stanford, Calif.
  • Sotlar K; Institute of Pathology, Paracelsus Medical University Salzburg, Salzburg, Austria.
  • Sperr WR; Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria; Ludwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria.
  • Degenfeld-Schonburg L; Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria; Ludwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria.
  • Smiljkovic D; Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria; Ludwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria.
  • Triggiani M; Division of Allergy and Clinical Immunology, University of Salerno, Salerno, Italy.
  • Horny HP; Institute of Pathology, Ludwig-Maximilian-University, Munich, Germany.
  • Arock M; Department of Hematological Biology, Pitié-Salpêtrière Charles-Foix Hospital, AP-HP Sorbonne University, Paris.
  • Galli SJ; Department of Pathology, Department of Microbiology and Immunology, and the Sean N. Parker Center for Allergy and Asthma Research, Stanford University School of Medicine, Stanford, Calif.
  • Metcalfe DD; Mast Cell Biology Section, Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md.
J Allergy Clin Immunol ; 149(6): 1866-1874, 2022 06.
Article in En | MEDLINE | ID: mdl-35421448
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mastocytosis / Mastocytosis, Systemic / Mast Cell Activation Disorders Type of study: Prognostic_studies Limits: Humans Language: En Journal: J Allergy Clin Immunol Year: 2022 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mastocytosis / Mastocytosis, Systemic / Mast Cell Activation Disorders Type of study: Prognostic_studies Limits: Humans Language: En Journal: J Allergy Clin Immunol Year: 2022 Document type: Article Country of publication: