TY - JOUR
T1 - Membrane IL-18 identifies a human macrophage subset with distinct proteomic and functional traits
AU - Vitale, Chiara
AU - Petretto, Andrea
AU - Cortese, Katia
AU - Carta, Sonia
AU - Dondero, Alessandra
AU - Lavarello, Chiara
AU - Cangelosi, Davide
AU - Morini, Martina
AU - Bellora, Francesca
AU - Arnaldi, Pietro
AU - Loiacono, Fabrizio
AU - Bruzzone, Santina
AU - Piacente, Francesco
AU - Bruno, Silvia
AU - Serra, Martina
AU - Pessino, Annamaria
AU - Mammoliti, Serafina
AU - Garaventa, Alberto
AU - Conte, Massimo
AU - Locati, Massimo
AU - Norata, Giuseppe Danilo
AU - Colonna, Marco
AU - Vivier, Eric
AU - Bottino, Cristina
AU - Castriconi, Roberta
N1 - Publisher Copyright:
© 2025 The Author(s). Published with license by Taylor & Francis Group, LLC.
PY - 2025
Y1 - 2025
N2 - 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.
AB - 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.
KW - adult cancer patients
KW - endocytosis
KW - FOLR2
KW - IL-18
KW - Macrophages
KW - pediatric neuroblastoma
KW - proteomic-analysis
KW - TREM2
UR - https://www.scopus.com/pages/publications/105020993372
U2 - 10.1080/2162402X.2025.2571774
DO - 10.1080/2162402X.2025.2571774
M3 - Article
C2 - 41194451
AN - SCOPUS:105020993372
SN - 2162-4011
VL - 14
JO - OncoImmunology
JF - OncoImmunology
IS - 1
M1 - 2571774
ER -