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Tailoring In Vivo Cytotoxicity Assays to Study Immunodominance in Tumor-specific CD8+ T Cell Responses
Published on: May 6, 2019
Preferential Recognition of Drug-Induced Altered Self-Presentation on Tumor Cells, but Not Host Cells, by CD8+ T
Takeshi Susukida1, Shigeki Aoki2, Yoshihiro Hayakawa1
1Section of Host Defences, Institute of Natural Medicine, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan.
We previously reported that CD8+ T cell activation via drug-induced altered self-presentation increases the tumor immunogenicity and cancer immunotherapy efficacy. Although the anti-human immunodeficiency virus drug abacavir (ABC) increases the tumor immunogenicity and induces CD8+ T cell anti-tumor immune responses in mice inoculated with tumor cells ectopically expressing the human leukocyte antigen (HLA)-B*57:01, whether such anti-tumor immunity is also triggered in hosts with high HLA-B*57:01 expression levels remain unclear. To verify this, we investigated the anti-tumor effects of ABC on HLA-B*57:01-expressing tumor and normal host cells using HLA-B*57:01 transgenic (B*57:01-Tg) mice in this study. ABC suppressed the HLA-B*57:01-expressing B16F10 tumor growth and increased the CD8+ T cell tumor infiltration in B*57:01-Tg mice. ABC also activated the tumor-infiltrating CD8+ T cells to secrete interferon-γ but did not promote their proliferation in the tumors of B*57:01-Tg mice. Moreover, ABC did not increase the effector CD8+ T cell proportions in the tumor-draining lymph nodes of B*57:01-Tg mice. Overall, CD8+ T cells preferentially recognized the ABC-induced altered self-antigen-presenting HLA-B*57:01-expressing tumor cells, but not host cells, to elicit anti-tumor immunity.
We previously reported that CD8+ T cell activation via drug-induced altered self-presentation increases the tumor immunogenicity and cancer immunotherapy efficacy. Although the anti-human immunodeficiency virus drug abacavir (ABC) increases the tumor immunogenicity and induces CD8+ T cell anti-tumor immune responses in mice inoculated with tumor cells ectopically expressing the human leukocyte antigen (HLA)-B*57:01, whether such anti-tumor immunity is also triggered in hosts with high HLA-B*57:01 expression levels remain unclear. To verify this, we investigated the anti-tumor effects of ABC on HLA-B*57:01-expressing tumor and normal host cells using HLA-B*57:01 transgenic (B*57:01-Tg) mice in this study. ABC suppressed the HLA-B*57:01-expressing B16F10 tumor growth and increased the CD8+ T cell tumor infiltration in B*57:01-Tg mice. ABC also activated the tumor-infiltrating CD8+ T cells to secrete interferon-γ but did not promote their proliferation in the tumors of B*57:01-Tg mice. Moreover, ABC did not increase the effector CD8+ T cell proportions in the tumor-draining lymph nodes of B*57:01-Tg mice. Overall, CD8+ T cells preferentially recognized the ABC-induced altered self-antigen-presenting HLA-B*57:01-expressing tumor cells, but not host cells, to elicit anti-tumor immunity.
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