Mice transgenic for human CTLA4-CD28 fusion gene show proliferation and transformation of ATLL-like and AITL-like T cells

Oncoimmunology. 2022 Jan 4;11(1):2015170. doi: 10.1080/2162402X.2021.2015170. eCollection 2022.

Abstract

CTLA4-CD28 gene fusion has been reported to occur in diverse types of T cell lymphoma. The fusion event is expected to convert inhibitory signals to activating signals and promote proliferation and potentially transformation of T cells. To test the function of the CTLA4-CD28 fusion gene in vivo, we generated a murine model that expresses the gene in a T cell-specific manner. The transgenic mice have shorter life spans and display inflammatory responses including lymphadenopathy and splenomegaly. T cells in turn show higher levels of activation and infiltrate various organs including the lung and skin. T cells, in particular CD4+ helper T cells, were also readily transplantable to immunocompromised mice. Transcriptomic profiling revealed that the gene expression pattern in CD4 + T cells closely resembles that of adult T cell leukemia/lymphoma (ATLL) and that of angioimmunoblastic T cell lymphoma (AITL) tissues. Consistently, we detected supernumerary FOXP3+ cells and PD-1+ cells in transgenic and transplanted mice. This is the first report demonstrating the transforming activity of the CTLA4-CD28 fusion gene in vivo, and this murine model should be useful in dissecting the molecular events downstream to this mutation.

Keywords: AITL; ATLL; CD28; CTLA4; fusion gene; murine model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD28 Antigens* / genetics
  • CTLA-4 Antigen / genetics
  • Cell Proliferation / genetics
  • Gene Fusion
  • Humans
  • Leukemia-Lymphoma, Adult T-Cell*
  • Mice
  • Mice, Transgenic
  • Oncogene Proteins, Fusion*

Substances

  • CD28 Antigens
  • CTLA-4 Antigen
  • CTLA4 protein, human
  • Oncogene Proteins, Fusion

Grants and funding

This work was supported by the National Research Foundation of Korea (NRF-2015K1A4A3047851, NRF-2020R1A2C2099719 & NRF-2019R1F1A1062011) funded by the Ministry of Science and ICT, Republic of Korea.