Tumor microenvironment of Burkitt lymphoma: different immune signatures with different clinical behavior

Author:

Siciliano Maria Chiara1,Bertolazzi Giorgio23ORCID,Morello Gaia2,Tornambè Salvatore1,Del Corvo Marcello4,Granai Massimo1,Sapienza Maria Rosaria4ORCID,Leahy Ciara I.5,Fennell Eanna5,Belmonte Beatrice2ORCID,Arcuri Felice1,Vannucchi Margherita1,Mancini Virginia1,Guazzo Raffaella1,Boccacci Roberto1,Onyango Noel6,Nyagol Joshua7,Santi Raffaella8,Di Stefano Gioia8,Ferrara Domenico1ORCID,Bellan Cristiana1,Marafioti Teresa9ORCID,Ott German10,Siebert Reiner11,Quintanilla-Fend Leticia12ORCID,Fend Falko12,Murray Paul5,Tripodo Claudio513ORCID,Pileri Stefano4,Lazzi Stefano1,Leoncini Lorenzo1

Affiliation:

1. 1Department of Medical Biotechnologies, University of Siena, Siena, Italy

2. 2Tumor Immunology Unit, Department of Health Sciences, University of Palermo, Palermo, Italy

3. 3Department of Economics, Business, and Statistics, University of Palermo, Palermo, Italy

4. 4Istituto Europeo di Oncologia (IEO), IRCSS Milano, Milan, Italy

5. 5School of Medicine, Bernal Institute, Health Research Institute and Limerick Digital Cancer Research Centre, University of Limerick, Limerick, Ireland

6. 6Department of Medical Microbiology and Immunology, University of Nairobi, Nairobi, Kenya

7. 7Department of Human Pathology, University of Nairobi, Nairobi, Kenya

8. 8Department of Pathology, University of Florence, Florence, Italy

9. 9Department of Cellular Pathology, University College London, London, United Kingdom

10. 10AbteilungfürKlinischePathologie, Robert-Bosch-Krankenhaus and Dr. Margarete Fischer-Bosch InstitutfürKlinischePharmakologie, Stuttgart, Germany

11. 11Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany

12. 12Institut für Pathologie und Neuropathologie, University of Tubingen, Tubingen, Germany

13. 13Tumor and Microenvironment Histopathology Unit, IFOM, the FIRC Institute of Molecular Oncology, Milan, Italy

Abstract

Abstract Burkitt lymphoma (BL) is characterized by a tumor microenvironment (TME) in which macrophages represent the main component, determining a distinct histological appearance known as “starry sky” pattern. However, in some instances, BL may exhibit a granulomatous reaction that has been previously linked to favorable prognosis and spontaneous regression. The aim of our study was to deeply characterize the immune landscape of 7 cases of Epstein-Barr virus–positive (EBV+) BL with granulomatous reaction compared with 8 cases of EBV+ BL and 8 EBV-negative (EBV–) BL, both with typical starry sky pattern, by Gene expression profiling performed on the NanoString nCounter platform. Subsequently, the data were validated using multiplex and combined immunostaining. Based on unsupervised clustering of differentially expressed genes, BL samples formed 3 distinct clusters differentially enriched in BL with a diffuse granulomatous reaction (cluster 1), EBV+ BL with typical starry sky pattern (cluster 2), EBV– BL with typical “starry sky” (cluster 3). We observed variations in the immune response signature among BL with granulomatous reaction and BL with typical “starry sky,” both EBV+ and EBV–. The TME signature in BL with diffuse granulomatous reaction showed a proinflammatory response, whereas BLs with “starry sky” were characterized by upregulation of M2 polarization and protumor response. Moreover, the analysis of additional signatures revealed an upregulation of the dark zone signature and epigenetic signature in BL with a typical starry sky. Tumor-associated macrophages and epigenetic regulators may be promising targets for additional therapies for BL lymphoma, opening novel immunotherapeutic strategies.

Publisher

American Society of Hematology

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