4.8 Article

TNFα blockade overcomes resistance to anti-PD-1 in experimental melanoma

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NATURE COMMUNICATIONS
卷 8, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-017-02358-7

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  1. Ligue nationale contre le cancer
  2. Ligue regionale contre le cancer
  3. Canceropole Grand Sud-Ouest
  4. INSERM Transfert
  5. Institut National du Cancer
  6. ROTARY Toulouse clubs
  7. Fondation Toulouse Cancer Sante
  8. INSERM
  9. Paul Sabatier University (Toulouse III)
  10. Prestige co-financing grant award (REA grant) [PCOFUND-GA-2013-609102]

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Antibodies against programmed cell death-1 (PD-1) have considerably changed the treatment for melanoma. However, many patients do not display therapeutic response or eventually relapse. Moreover, patients treated with anti-PD-1 develop immune-related adverse events that can be cured with anti-tumor necrosis factor alpha (TNF) antibodies. Whether anti-TNF antibodies affect the anti-cancer immune response remains unknown. Our recent work has highlighted that TNFR1-dependent TNF signalling impairs the accumulation of CD8+ tumorinfiltrating T lymphocytes (CD8+ TILs) in mouse melanoma. Herein, our results indicate that TNF or TNFR1 blockade synergizes with anti-PD-1 on anti-cancer immune responses towards solid cancers. Mechanistically, TNF blockade prevents anti-PD-1-induced TIL cell death as well as PD-L1 and TIM-3 expression. TNF expression positively correlates with expression of PD-L1 and TIM-3 in human melanoma specimens. This study provides a strong rationale to develop a combination therapy based on the use of anti-PD-1 and anti-TNF in cancer patients.

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