Tumour-infiltrating bystander CD8⁺ T cells activated by IL-15 contribute to tumour control in non-small cell lung cancer.

Abstract

Tumour-unrelated, virus-specific bystander CD8⁺ T cells were recently shown to be abundant among tumour-infiltrating lymphocytes (TILs). However, their roles in tumour immunity have not been elucidated yet. We studied the characteristics of bystander CD8⁺ TILs from non-small cell lung cancer (NSCLC) tissues (N=66) and their activation by interleukin (IL)-15 to repurpose them for tumour immunotherapy. We show that bystander CD8⁺ TILs specific to various viruses are present in human NSCLC tissues. We stimulated CD8⁺ TILs ex vivo using IL-15 without cognate antigens and found that IL-15 treatment upregulated NKG2D expression on CD8⁺ TILs, resulting in NKG2D-dependent production of interferon (IFN)-γ (p=0.0006). Finally, we tested whether IL-15 treatment can control tumour growth in a murine NSCLC model with or without a history of murine cytomegalovirus (MCMV) infection. IL-15 treatment reduced the number of tumour nodules in the lung only in mice with MCMV infection (p=0.0037). We confirmed that MCMV-specific bystander CD8⁺ TILs produced interferon (IFN)-γ after IL-15 treatment, and that IL-15 treatment in MCMV-infected mice upregulated tumour necrosis factor-α and IFN-γ responsive genes in tumour microenvironment. Thus, the study demonstrates that bystander CD8⁺ TILs can be repurposed by IL-15 for tumour immunotherapy.