Membrane IL-18 identifies a human macrophage subset with distinct proteomic and functional traits

  • Chiara Vitale
  • , Andrea Petretto
  • , Katia Cortese
  • , Sonia Carta
  • , Alessandra Dondero
  • , Chiara Lavarello
  • , Davide Cangelosi
  • , Martina Morini
  • , Francesca Bellora
  • , Pietro Arnaldi
  • , Fabrizio Loiacono
  • , Santina Bruzzone
  • , Francesco Piacente
  • , Silvia Bruno
  • , Martina Serra
  • , Annamaria Pessino
  • , Serafina Mammoliti
  • , Alberto Garaventa
  • , Massimo Conte
  • , Massimo Locati
  • Giuseppe Danilo Norata, Marco Colonna, Eric Vivier, Cristina Bottino, Roberta Castriconi

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

This study contributes to the characterization of human macrophages in normal and pathological conditions such as cancer. We characterized a macrophage population expressing membrane-associated IL-18 (mIL-18) that shows peculiar proteomic, phenotypic, ultrastructural, and functional properties. mIL-18+ macrophages exhibit increased levels of key proteins involved in pathogen recognition, activation, migration, and endocytosis. They also display specialized functions in vesicle and actin filament transport and lipid metabolism, and have typical mitochondrial traits. Importantly, mIL-18+ cells dominate the peritoneal fluid of adult cancer patients and are present in the bone marrow of children with neuroblastoma. They express high levels of TREM2 but display heterogeneous FOLR2 expression, distinguishing distinct cell subsets with possibly different functions. Accordingly, in primary neuroblastomas, transcriptional signatures associated with mIL-18 expression show different prognostic values. Our data show that mIL-18+ macrophages, which are predominant across the tumor microenvironment, exhibit previously undetected heterogeneity, potentially impacting tumor progression in a variable manner.

Original languageEnglish
Article number2571774
JournalOncoImmunology
Volume14
Issue number1
DOIs
StatePublished - 2025

Keywords

  • adult cancer patients
  • endocytosis
  • FOLR2
  • IL-18
  • Macrophages
  • pediatric neuroblastoma
  • proteomic-analysis
  • TREM2

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