TY - JOUR
T1 - Selected recent advances in understanding the role of human mast cells in health and disease
AU - Levi-Schaffer, Francesca
AU - Gibbs, Bernhard F
AU - Hallgren, Jenny
AU - Pucillo, Carlo
AU - Redegeld, Frank
AU - Siebenhaar, Frank
AU - Vitte, Joana
AU - Mezouar, Soraya
AU - Michel, Moïse
AU - Puzzovio, Pier Giorgio
AU - Maurer, Marcus
N1 - Funding Information:
F.L.-S. received funding from the Rosetrees Trust (UK), Aimwell Charitable Trust (UK), Israel Science Foundation (grant no. 442/18), Israel Ministry of Science & Technology , and Emalie Gutterman Memorial Endowed Fund for COPD Related Research (USA). F.L.S. is affiliated with the Adolph and Klara Brettler Center for Molecular Pharmacology and Therapeutics at the School of Pharmacy of The Hebrew University of Jerusalem . J.H. received funding from the Swedish Research Council , Swedish Heart-Lung Foundation , Knut and Alice Wallenberg Foundation , Malin and Lennart Philipson Foundation , Konsul ThC Bergh’s Foundation , Hans von Kantzow Foundation , Ruth och Nils-Erik Stenbäck Foundation , and Mary Kay Foundation . J.V. received personal funding as associate professor from Aix-Marseille University, Faculty of Medicine, Marseille, France, MEPHI, IHU Méditerranée Infection, Marseille, France, and University Hospitals of Marseille, Marseille, France; is a nonpaid visiting researcher at IDESP INSERM UMR UA 11, University of Montpellier, Montpellier, France; and received research grants from Fondation de France/Agence Nationale pour la Recherche , IHU Méditerranée Infection, French Society of Allergology , and European Academy of Allergy and Clinical Immunology . S.M. received personal funding as a researcher from Aix-Marseille University, Marseille, France. M.M. received personal funding as an associate practitioner from University Hospitals of Nimes, Nîmes, France.
Funding Information:
F.L.-S. received funding from the Rosetrees Trust (UK), Aimwell Charitable Trust (UK), Israel Science Foundation (grant no. 442/18), Israel Ministry of Science & Technology, and Emalie Gutterman Memorial Endowed Fund for COPD Related Research (USA). F.L.S. is affiliated with the Adolph and Klara Brettler Center for Molecular Pharmacology and Therapeutics at the School of Pharmacy of The Hebrew University of Jerusalem. J.H. received funding from the Swedish Research Council, Swedish Heart-Lung Foundation, Knut and Alice Wallenberg Foundation, Malin and Lennart Philipson Foundation, Konsul ThC Bergh's Foundation, Hans von Kantzow Foundation, Ruth och Nils-Erik Stenb?ck Foundation, and Mary Kay Foundation. J.V. received personal funding as associate professor from Aix-Marseille University, Faculty of Medicine, Marseille, France, MEPHI, IHU M?diterran?e Infection, Marseille, France, and University Hospitals of Marseille, Marseille, France; is a nonpaid visiting researcher at IDESP INSERM UMR UA 11, University of Montpellier, Montpellier, France; and received research grants from Fondation de France/Agence Nationale pour la Recherche, IHU M?diterran?e Infection, French Society of Allergology, and European Academy of Allergy and Clinical Immunology. S.M. received personal funding as a researcher from Aix-Marseille University, Marseille, France. M.M. received personal funding as an associate practitioner from University Hospitals of Nimes, N?mes, France. Disclosure of potential conflict of interest: F. Siebenhaar is or recently was a speaker and/or advisor for and/or has received research funding from Allakos, Blueprint, Celldex, CogentBio, Genentech, Novartis, Moxie, Sanofi, and Uriach. J. Vitte reports speaker and consultancy fees in the past 5 years from Meda Pharma (Mylan), Novartis, Sanofi, and Thermo Fisher Scientific, outside the submitted work. M. Maurer is or recently was a speaker and/or advisor for and/or has received research funding from Allakos, Amgen, Aralez, ArgenX, AstraZeneca, Celldex, Centogene, CSL Behring, FAES, Genentech, GIInnovation, Innate Pharma, Kyowa Kirin, Leo Pharma, Lilly, Menarini, Moxie, Novartis, Roche, Sanofi/Regeneron, Third HarmonicBio, UCB, and Uriach. The rest of the authors declare that they have no relevant conflicts of interest.
Publisher Copyright:
© 2022 American Academy of Allergy, Asthma & Immunology
Published by Elsevier Inc. All rights reserved.
PY - 2022/6
Y1 - 2022/6
N2 - Mast cells are highly granular tissue-resident cells and key drivers of inflammation, particularly in allergies as well as in other inflammatory diseases. Most mast cell research was initially conducted in rodents but has increasingly shifted to the human system, with the advancement of research technologies and methodologies. Today we can analyze primary human cells including rare subpopulations, we can produce and maintain mast cells isolated from human tissues, and there are several human mast cell lines. These tools have substantially facilitated our understanding of their role and function in different organs in both health and disease. We can now define more clearly where human mast cells originate from, how they develop, which mediators they store, produce de novo, and release, how they are activated and by which receptors, and which neighboring cells they interact with and by which mechanisms. Considerable progress has also been made regarding the potential contribution of mast cells to disease, which, in turn, has led to the development of novel approaches for preventing key pathogenic effects of mast cells, heralding the era of mast cell–targeted therapeutics. In this review, we present and discuss a selection of some of the most significant advancements and remaining gaps in our understanding of human mast cells during the last 25 years, with a focus on clinical relevance.
AB - Mast cells are highly granular tissue-resident cells and key drivers of inflammation, particularly in allergies as well as in other inflammatory diseases. Most mast cell research was initially conducted in rodents but has increasingly shifted to the human system, with the advancement of research technologies and methodologies. Today we can analyze primary human cells including rare subpopulations, we can produce and maintain mast cells isolated from human tissues, and there are several human mast cell lines. These tools have substantially facilitated our understanding of their role and function in different organs in both health and disease. We can now define more clearly where human mast cells originate from, how they develop, which mediators they store, produce de novo, and release, how they are activated and by which receptors, and which neighboring cells they interact with and by which mechanisms. Considerable progress has also been made regarding the potential contribution of mast cells to disease, which, in turn, has led to the development of novel approaches for preventing key pathogenic effects of mast cells, heralding the era of mast cell–targeted therapeutics. In this review, we present and discuss a selection of some of the most significant advancements and remaining gaps in our understanding of human mast cells during the last 25 years, with a focus on clinical relevance.
KW - Allergy
KW - cancer
KW - human mast cells
KW - receptors
KW - signal transduction
UR - http://www.scopus.com/inward/record.url?scp=85127360336&partnerID=8YFLogxK
U2 - 10.1016/j.jaci.2022.01.030
DO - 10.1016/j.jaci.2022.01.030
M3 - Review article
C2 - 35276243
SN - 0091-6749
VL - 149
SP - 1833
EP - 1844
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 6
ER -