4.8 Review

Pathologically Relevant Mouse Models for Epstein-Barr Virus-Associated B Cell Lymphoma

Journal

FRONTIERS IN IMMUNOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.639844

Keywords

Epstein-Barr virus; B cell lymphoma; immune surveillance; mouse model; lymphoproliferative disease

Categories

Funding

  1. Japan Society for the Promotion of Science (JSPS) [18H02669, 19K22538, 17H06937]
  2. Senshin Medical Research Foundation
  3. Friends of Leukemia Research Fund
  4. Core Research for Organelle Diseases in Hiroshima University (MEXT program for promoting the enhancement of research universities, Japan)
  5. Grants-in-Aid for Scientific Research [18H02669, 19K22538, 17H06937] Funding Source: KAKEN

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The Epstein-Barr virus is common in humans and can lead to lymphoproliferative diseases which may develop into lymphoma. The immune system plays a role in monitoring EBV+ B cells to prevent tumor formation.
The Epstein-Barr virus (EBV) is endemic in humans and can efficiently transform infected B cells under some circumstances. If an EBV carrier experiences immune suppression, EBV+ B cells can turn into lymphoblasts and exhibit growth expansion that may cause lymphoproliferative diseases which often develop into lymphoma. Our immune system conducts surveillance for EBV+ B cells in order to block spontaneous tumor formation. Here, we summarize the EBV products involved in tumorigenesis, EBV-associated lymphomas, and pathologically relevant mouse models. Preclinical mouse models for a range of EBV-associated diseases not only clear the path to new therapeutic approaches but also aid in our understanding of the nature of lymphomagenesis and immune surveillance.

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