1. Comment on 'Tumor-initiating cells establish an IL-33–TGF-β niche signaling loop to promote cancer progression'
- Author
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Julien Stackowicz, Aurélie Mougel, Pierre Bruhns, Jinmiao Chen, Eva Conde, William P. M. Worrall, Rebecca Gentek, Jasper B. J. Kamphuis, Nicolas Gaudenzio, Laurent L. Reber, Laurent Guilleminault, Emilie Mauré, Institut Toulousain des Maladies Infectieuses et Inflammatoires (Infinity), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Sorbonne Université (SU), Anticorps en thérapie et pathologie - Antibodies in Therapy and Pathology, Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Pasteur [Paris], CHU Toulouse [Toulouse], Unité différenciation épidermique et auto-immunité rhumatoïde (UDEAR), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM), Singapore Immunology Network (SIgN), Biomedical Sciences Institute (BMSI), University of Edinburgh, Supported by a fellowship from the Institut National de la Santé et de la Recherche Médicale (INSERM) ATIP-Avenir program (J.B.J.K.), a fellowship from INSERM-Region Occitanie (W.P.M.W.), the European Research Council (ERC)–Seventh Framework Program (ERC-2013-CoG 616050), the Institut Pasteur, and INSERM (P.B.), the Société Française de Dermatologie (SFD), the Société Française d’Allergologie (SFA), the Marie Skłodowska-Curie Individual Fellowship (H2020-MSCA-IF-2016 #749629), the European Research Council (ERC-2018-STG #802041), and the INSERM ATIP-Avenir program (N.G.), a Chancellor’s Fellowship of the University of Edinburgh and a Senior Research Fellowship from the Kennedy Trust for Rheumatology Research (R.G.), and the INSERM ATIP-Avenir program (L.L.R.), European Project: 616050,EC:FP7:ERC,ERC-2013-CoG,MYELOSHOCK(2014), European Project: 802041, European Project: 749629,H2020-EU.1.3.2. - Nurturing excellence by means of cross-border and cross-sector mobility ,H2020-MSCA-IF-2016,NEMESIS(2017), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM), Bruhns, Pierre, Role of myeloid cells, their mediators and their antibody receptors in allergic shock (anaphylaxis) using humanized mouse models and clinical samples - MYELOSHOCK - - EC:FP7:ERC2014-09-01 - 2019-08-31 - 616050 - VALID, ERC-2018-STG - 802041 - INCOMING, and Neuron/mast cell interactions in skin diseases - NEMESIS - - H2020-EU.1.3.2. - Nurturing excellence by means of cross-border and cross-sector mobility 2017-07-01 - 2019-06-30 - 749629 - VALID
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0301 basic medicine ,[SDV.IMM] Life Sciences [q-bio]/Immunology ,[SDV]Life Sciences [q-bio] ,medicine.medical_treatment ,MESH: Receptors, IgE ,Immunoglobulin E ,03 medical and health sciences ,0302 clinical medicine ,Transforming Growth Factor beta ,Neoplasms ,medicine ,Humans ,Receptor ,MESH: Transforming Growth Factor beta ,MESH: Humans ,Multidisciplinary ,biology ,Receptors, IgE ,Cancer ,Transforming growth factor beta ,Interleukin-33 ,medicine.disease ,MESH: Interleukin-33* / genetics ,MESH: Neoplastic Stem Cells ,3. Good health ,[SDV] Life Sciences [q-bio] ,Interleukin 33 ,MESH: Neoplasms* / genetics ,030104 developmental biology ,Cytokine ,030220 oncology & carcinogenesis ,Neoplastic Stem Cells ,biology.protein ,Cancer research ,[SDV.IMM]Life Sciences [q-bio]/Immunology ,Antibody ,Transforming growth factor - Abstract
Taniguchi et al . (Research Articles, 17 July 2020, p. 269) claim that the cytokine interleukin-33 induces accumulation of tumor-associated macrophages expressing the immunoglobulin E receptor FcεRI. Although these findings hold great therapeutic promise, we provide evidence that the anti-FcεRI antibody used in this study is not specific for FcεRI on macrophages, which raises concerns about the validity of some of the conclusions.
- Published
- 2021
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