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The Number of MRGPRX2-Expressing Cells Is Increased in Skin Lesions of Patients With Indolent Systemic Mastocytosis, But Is Not Linked to Symptom Severity

  • Polina Pyatilova
  • , Tameem Ashry
  • , Yanyan Luo
  • , Jiajun He
  • , Hanna Bonnekoh
  • , Qingqing Jiao
  • , Sherezade Moñino-Romero
  • , Man Hu
  • , Jörg Scheffel
  • , Stefan Frischbutter
  • , Maud A.W. Hermans
  • , Bradford A. Youngblood
  • , Marcus Maurer
  • , Frank Siebenhaar
  • , Pavel Kolkhir*
  • *Corresponding author for this work
  • Charité – Universitätsmedizin Berlin
  • Fraunhofer Institute for Translational Medicine and Pharmacology (ITMP)
  • King Saud University
  • Southwest Medical University
  • Soochow University
  • Allakos Inc.

Research output: Contribution to journalArticleAcademicpeer-review

18 Citations (Scopus)
101 Downloads (Pure)

Abstract

Background: Recently, the expression of the mast cell (MC) receptor Mas-related G protein–coupled receptor X2 (MRGPRX2) has been detected in lesional skin of adult patients with cutaneous mastocytosis. As of yet, little is known about the clinical relevance of MRGPRX2 and its agonists in patients with mastocytosis, including indolent systemic mastocytosis (ISM). Methods: MRGPRX2 and MRGPRX2 agonists, cortistatin (CST), and major basic protein (MBP) were analyzed in lesional and non-lesional skin of patients with ISM and skin of healthy controls by immunohistochemistry. Co-localization of MRGPRX2 and MRGPRX2-mRNA with the MC marker tryptase was assessed by immunofluorescence microscopy and in situ hybridization, respectively. We assessed clinical, demographic, and laboratory data, including mastocytosis activity score (MAS), serum tryptase, and KIT D816V allele burden. Results: The number of MRGPRX2-expressing (MRGPRX2+) cells, MRGPRX2-mRNA+ MCs, and CST-expressing (CST+) and MBP-expressing (MBP+) cells was significantly higher in lesional skin as compared to non-lesional skin and/or skin of healthy controls (all p < 0.05). Increased numbers of MRGPRX2+ cells, MRGPRX2-mRNA+ MCs, and CST+ and MBP+ cells were not associated with clinical and laboratory features of ISM, including disease burden, symptom severity, evidence of anaphylaxis, and tryptase levels. Conclusions: Skin lesions of patients with ISM showed high numbers of MRGPRX2+ cells, although they were not linked to symptom severity. Clinical relevance of the MRGPRX2-mediated pathway of MC activation in ISM remains unclear and should be investigated in further studies.

Original languageEnglish
Article number930945
JournalFrontiers in Immunology
Volume13
DOIs
Publication statusPublished - 26 Jul 2022

Bibliographical note

Funding Information:
This study was in part financially supported by Allakos Inc. The funder was not involved in the study design, collection, analysis, interpretation of data, the writing of this article, or decision to submit it for publication.

Publisher Copyright:
Copyright © 2022 Pyatilova, Ashry, Luo, He, Bonnekoh, Jiao, Moñino-Romero, Hu, Scheffel, Frischbutter, Hermans, Youngblood, Maurer, Siebenhaar and Kolkhir.

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