Epstein–Barr Virus and the Pathogenesis of Diffuse Large B-Cell Lymphoma

Author:

Ross Aisling12ORCID,Leahy Ciara12,Neylon Fiona12,Steigerova Jana3,Flodr Patrik34,Navratilova Martina34,Urbankova Helena5ORCID,Vrzalikova Katerina6,Mundo Lucia17,Lazzi Stefano7,Leoncini Lorenzo7,Pugh Matthew6ORCID,Murray Paul13

Affiliation:

1. Health Research Institute and School of Medicine, University of Limerick, V94 T9PX Limerick, Ireland

2. BioScience and BioEngineering Research (BioSciBer), Bernal BioMaterials Cluster, Bernal Institute, University of Limerick, V94 T9PX Limerick, Ireland

3. Department of Clinical and Molecular Pathology, Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University Olmouc, 775 15 Olomouc, Czech Republic

4. Department of Clinical and Molecular Pathology, University Hospital Olomouc, 779 00 Olomouc, Czech Republic

5. Department of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky Univesity and University Hospital Olomouc, 779 00 Olomouc, Czech Republic

6. Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham B15 2TT, UK

7. Department of Medical Biotechnologies, Section of Pathology, University of Siena, 53100 Siena, Italy

Abstract

Epstein–Barr virus (EBV), defined as a group I carcinogen by the World Health Organization (WHO), is present in the tumour cells of patients with different forms of B-cell lymphoma, including Burkitt lymphoma, Hodgkin lymphoma, post-transplant lymphoproliferative disorders, and, most recently, diffuse large B-cell lymphoma (DLBCL). Understanding how EBV contributes to the development of these different types of B-cell lymphoma has not only provided fundamental insights into the underlying mechanisms of viral oncogenesis, but has also highlighted potential new therapeutic opportunities. In this review, we describe the effects of EBV infection in normal B-cells and we address the germinal centre model of infection and how this can lead to lymphoma in some instances. We then explore the recent reclassification of EBV+ DLBCL as an established entity in the WHO fifth edition and ICC 2022 classifications, emphasising the unique nature of this entity. To that end, we also explore the unique genetic background of this entity and briefly discuss the potential role of the tumour microenvironment in lymphomagenesis and disease progression. Despite the recent progress in elucidating the mechanisms of this malignancy, much work remains to be done to improve patient stratification, treatment strategies, and outcomes.

Funder

Blood Cancer UK

Cancer Research UK Birmingham Centre, University of Birmingham, Birmingham, United Kingdom

European Regional Development Fund Project

Marie Skłodowska-Curie Actions grant funding at the University of Limerick

Publisher

MDPI AG

Subject

Paleontology,Space and Planetary Science,General Biochemistry, Genetics and Molecular Biology,Ecology, Evolution, Behavior and Systematics

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