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

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作者
Florie Bertrand
Anne Montfort
Elie Marcheteau
Caroline Imbert
Julia Gilhodes
Thomas Filleron
Philippe Rochaix
Nathalie Andrieu-Abadie
Thierry Levade
Nicolas Meyer
Céline Colacios
Bruno Ségui
机构
[1] INSERM UMR 1037,Laboratoire de Biochimie
[2] CRCT,Institut Universitaire du Cancer
[3] Equipe Labellisée Ligue Contre Le Cancer,undefined
[4] Université Toulouse III - Paul Sabatier,undefined
[5] Université Fédérale de Toulouse Midi-Pyrénées,undefined
[6] Institut Universitaire du Cancer,undefined
[7] Institut Fédératif de Biologie,undefined
[8] Toulouse,undefined
[9] Hôpital Larrey et Oncopôle,undefined
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摘要
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 α (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+ tumor-infiltrating 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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