Abstract

Bovine leukemia virus (BLV) is a retrovirus that infects B cells in cattle and causes bovine leukosis after a long latent period. Progressive exhaustion of T cell functions is considered to facilitate disease progression of BLV infection. Programmed death-1 (PD-1) and lymphocyte activation gene-3 (LAG-3) are immunoinhibitory receptors that contribute to T-cell exhaustion caused by BLV infection in cattle. However, it is unclear whether the cooperation of PD-1 and LAG-3 accelerates disease progression of BLV infection. In this study, multi-color flow cytometric analyses of PD-1- and LAG-3-expressing T cells were performed in BLV-infected cattle at different stages of the disease. The frequencies of PD-1+LAG-3+ heavily exhausted T cells among CD4+ and CD8+ T cells was higher in the blood of cattle with B-cell lymphoma over that of BLV-uninfected and BLV-infected cattle without lymphoma. In addition, blockade assays of peripheral blood mononuclear cells were performed to examine whether inhibition of the interactions between PD-1 and LAG-3 and their ligands by blocking antibodies could restore T-cell function during BLV infection. Single or dual blockade of the PD-1 and LAG-3 pathways reactivated the production of Th1 cytokines, interferon-γ and tumor necrosis factor-α, from BLV-specific T cells of the infected cattle. Taken together, these results indicate that PD-1 and LAG-3 cooperatively mediate the functional exhaustion of CD4+ and CD8+ T cells and are associated with the development of B-cell lymphoma in BLV-infected cattle.

Highlights

  • Bovine leukemia virus (BLV) is a member of the genus Deltaretrovirus and is genetically related to human T-cell leukemia virus type 1 [1]

  • Increased frequencies of heavily exhausted ­CD4+ and ­CD8+ T cells in BLV‐infected cattle with B‐cell lymphoma Earlier studies have shown that immunoinhibitory receptors such as programmed death-1 (PD-1) and lymphocyte activation gene-3 (LAG-3) were upregulated and play an immunomodulatory role in T-cell exhaustion during BLV infection in cattle [13,14,15]

  • The cell-surface expression of PD-1 and LAG-3 on C­ D4+, ­CD8+, and γδ T cells was investigated by multi-color flow cytometry of peripheral blood mononuclear cells (PBMCs) isolated from BLV-infected cattle in different disease stages (AL, persistent lymphocytosis (PL), and enzootic bovine leukosis (EBL))

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Summary

Introduction

Bovine leukemia virus (BLV) is a member of the genus Deltaretrovirus (subfamily Orthoretrovirinae, family Retroviridae) and is genetically related to human T-cell leukemia virus type 1 [1]. BLV infects B cells in cattle and is integrated into the host genome as a provirus [2, 3]. Up to 30% of infected cattle develop persistent lymphocytosis (PL), characterized by non-malignant polyclonal expansion of ­IgM+CD5+ B cells, the majority of which harbor BLV provirus. After a long latent period, less than 5% of infected cattle develop malignant B-cell. To develop strategies to induce effective immune responses to BLV infection, previous studies have investigated the mechanism responsible for T-cell exhaustion [13,14,15,16]. A previous report has shown that the immunoinhibitory receptor programmed death-1 (PD-1) is upregulated in ­CD4+ and ­CD8+ T cells and is involved in the exhaustion of T-cell functions in BLV-infected cattle bearing B-cell lymphoma [13]. Further studies have confirmed the correlation between upregulation of lymphocyte activation gene-3 (LAG-3) on ­CD4+ and ­CD8+

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