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Mast cells as a unique hematopoietic lineage and cell system: From Paul Ehrlich's visions to precision medicine concepts

  • Peter Valent
  • , Cem Akin
  • , Karin Hartmann
  • , Gunnar Nilsson
  • , Andreas Reiter
  • , Olivier Hermine
  • , Karl Sotlar
  • , Wolfgang R. Sperr
  • , Luis Escribano
  • , Tracy I. George
  • , Hanneke C. Kluin-Nelemans
  • , Celalettin Ustun
  • , Massimo Triggiani
  • , Knut Brockow
  • , Jason Gotlib
  • , Alberto Orfao
  • , Petri T. Kovanen
  • , Emir Hadzijusufovic
  • , Irina Sadovnik
  • , Hans Peter Horny
  • Michel Arock, Lawrence B. Schwartz, K. Frank Austen, Dean D. Metcalfe, Stephen J. Galli
  • Medical University of Vienna
  • University of Michigan, Ann Arbor
  • University of Basel
  • Karolinska Institutet at Karolinska University Hospital
  • Universitätsmedizin Mannheim
  • Univ-Paris Diderot Sorbonne Paris-Cité
  • University Children’s Hospital
  • Consejo Superior de Investigaciones Científicas
  • University of Utah School of Medicine
  • University Medical Center Groningen
  • University of Minnesota Medical School
  • University of Salerno
  • Stanford Cancer Institute
  • Wihuri Research Institute Finland
  • University of Veterinary Medicine Vienna
  • University of Munich
  • University Paris-Descartes
  • Virginia Commonwealth University
  • Harvard Medical School
  • National Institute of Allergy and Infectious Diseases (NIAID)
  • Stanford University School of Medicine

Research output: Contribution to journalReview articlepeer-review

170 Scopus citations

Abstract

The origin and functions of mast cells (MCs) have been debated since their description by Paul Ehrlich in 1879. MCs have long been considered 'reactive bystanders' and 'amplifiers' in inflammatory processes, allergic reactions, and host responses to infectious diseases. However, knowledge about the origin, phenotypes and functions of MCs has increased substantially over the past 50 years. MCs are now known to be derived from multipotent hematopoietic progenitors, which, through a process of differentiation and maturation, form a unique hematopoietic lineage residing in multiple organs. In particular, MCs are distinguishable from basophils and other hematopoietic cells by their unique phenotype, origin(s), and spectrum of functions, both in innate and adaptive immune responses and in other settings. The concept of a unique MC lineage is further supported by the development of a distinct group of neoplasms, collectively referred to as mastocytosis, in which MC precursors expand as clonal cells. The clinical consequences of the expansion and/or activation of MCs are best established in mastocytosis and in allergic inflammation. However, MCs have also been implicated as important participants in a number of additional pathologic conditions and physiological processes. In this article, we review concepts regarding MC development, factors controlling MC expansion and activation, and some of the fundamental roles MCs may play in both health and disease. We also discuss new concepts for suppressing MC expansion and/or activation using molecularly-targeted drugs.

Original languageEnglish
Pages (from-to)10743-10768
Number of pages26
JournalTheranostics
Volume10
Issue number23
DOIs
StatePublished - 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Histamine
  • IgE receptor
  • KIT
  • Mast cell activation
  • Mastocytosis
  • Tryptase

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