Publications

Surface CD52, CD84, and PTGER2 mark mature PMN-MDSCs from cancer patients and G-CSF-treated donors  (2024)

Authors:
Pettinella, Francesca; Mariotti, Barbara; Lattanzi, Chiara; Bruderek, Kirsten; Donini, Marta; Costa, Sara; Marini, Olivia; Iannoto, Giulia; Gasperini, Sara; Caveggion, Elena; Castellucci, Monica; Calzetti, Federica; Bianchetto-Aguilera, Francisco; Gardiman, Elisa; Giani, Matteo; Dusi, Stefano; Cantini, Maurizio; Vassanelli, Aurora; Pavone, Denise; Milella, Michele; Pilotto, Sara; Biondani, Pamela; Höing, Benedikt; Schleupner, Marie Carolin; Hussain, Timon; Hadaschik, Boris; Kaspar, Cordelia; Visco, Carlo; Tecchio, Cristina; Koenderman, Leo; Bazzoni, Flavia; Tamassia, Nicola; Brandau, Sven; Cassatella, Marco A.; Scapini, Patrizia
Title:
Surface CD52, CD84, and PTGER2 mark mature PMN-MDSCs from cancer patients and G-CSF-treated donors
Year:
2024
Type of item:
Articolo in Rivista
Tipologia ANVUR:
Articolo su rivista
Language:
Inglese
Format:
Elettronico
Referee:
No
Name of journal:
CELL REPORTS MEDICINE
ISSN of journal:
2666-3791
N° Volume:
5
Number or Folder:
2
Page numbers:
1-28
Keyword:
G-CSF; PMN-MDSCs; biomarkers; cancer patients; neutrophils
Short description of contents:
: Precise molecular characterization of circulating polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs) is hampered by their mixed composition of mature and immature cells and lack of specific markers. Here, we focus on mature CD66b+CD10+CD16+CD11b+ PMN-MDSCs (mPMN-MDSCs) from either cancer patients or healthy donors receiving G-CSF for stem cell mobilization (GDs). By RNA sequencing (RNA-seq) experiments, we report the identification of a distinct gene signature shared by the different mPMN-MDSC populations under investigation, also validated in mPMN-MDSCs from GDs and tumor-associated neutrophils (TANs) by single-cell RNA-seq (scRNA-seq) experiments. Analysis of such a gene signature uncovers a specific transcriptional program associated with mPMN-MDSC differentiation and allows us to identify that, in patients with either solid or hematologic tumors and in GDs, CD52, CD84, and prostaglandin E receptor 2 (PTGER2) represent potential mPMN-MDSC-associated markers. Altogether, our findings indicate that mature PMN-MDSCs distinctively undergo specific reprogramming during differentiation and lay the groundwork for selective immunomonitoring, and eventually targeting, of mature PMN-MDSCs.
Product ID:
137801
Handle IRIS:
11562/1119514
Last Modified:
October 16, 2024
Bibliographic citation:
Pettinella, Francesca; Mariotti, Barbara; Lattanzi, Chiara; Bruderek, Kirsten; Donini, Marta; Costa, Sara; Marini, Olivia; Iannoto, Giulia; Gasperini, Sara; Caveggion, Elena; Castellucci, Monica; Calzetti, Federica; Bianchetto-Aguilera, Francisco; Gardiman, Elisa; Giani, Matteo; Dusi, Stefano; Cantini, Maurizio; Vassanelli, Aurora; Pavone, Denise; Milella, Michele; Pilotto, Sara; Biondani, Pamela; Höing, Benedikt; Schleupner, Marie Carolin; Hussain, Timon; Hadaschik, Boris; Kaspar, Cordelia; Visco, Carlo; Tecchio, Cristina; Koenderman, Leo; Bazzoni, Flavia; Tamassia, Nicola; Brandau, Sven; Cassatella, Marco A.; Scapini, Patrizia, Surface CD52, CD84, and PTGER2 mark mature PMN-MDSCs from cancer patients and G-CSF-treated donors «CELL REPORTS MEDICINE» , vol. 5 , n. 22024pp. 1-28

Consulta la scheda completa presente nel repository istituzionale della Ricerca di Ateneo IRIS

<<back

Activities

Research facilities

Share