Chemotherapy-induced antitumor immunity requires formyl peptide receptor 1

被引:431
作者
Vacchelli, Erika [1 ,2 ,3 ,4 ,5 ]
Ma, Yuting [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
Baracco, Elisa E. [1 ,2 ,3 ,9 ]
Sistigu, Antonella [10 ]
Enot, David P. [1 ,2 ,3 ,11 ]
Pietrocola, Federico [1 ,2 ,3 ,9 ]
Yang, Heng [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
Adjemian, Sandy [1 ,2 ,3 ]
Chaba, Kariman [1 ,2 ,3 ,4 ]
Semeraro, Michaela [1 ,12 ,13 ]
Signore, Michele [14 ]
De Ninno, Adele [15 ]
Lucarini, Valeria [14 ]
Peschiaroli, Francesca [14 ]
Businaro, Luca [15 ]
Gerardino, Annamaria [15 ]
Manic, Gwenola [10 ]
Ulas, Thomas [16 ]
Guenther, Patrick [16 ]
Schultze, Joachim L. [16 ]
Kepp, Oliver [1 ,2 ,3 ,4 ,5 ]
Stoll, Gautier [1 ,2 ,3 ,4 ,5 ]
Lefebvre, Celine [1 ,17 ]
Mulot, Claire [18 ,19 ]
Castoldi, Francesca [1 ,2 ,3 ,9 ,20 ]
Rusakiewicz, Sylvie [1 ,12 ,13 ]
Ladoire, Sylvain [21 ,22 ,23 ]
Apetoh, Lionel [21 ,22 ,23 ]
Bravo-San Pedro, Jose Manuel [1 ,2 ,3 ,4 ,5 ]
Lucattelli, Monica [24 ]
Delarasse, Cecile [25 ]
Boige, Valerie [19 ,26 ]
Ducreux, Michel [9 ,26 ]
Delaloge, Suzette [17 ,27 ]
Borg, Christophe [28 ]
Andre, Fabrice [1 ,17 ,29 ,30 ]
Schiavoni, Giovanna [14 ]
Vitale, Ilio [10 ,31 ]
Laurent-Puig, Pierre [18 ,19 ,32 ]
Mattei, Fabrizio [14 ]
Zitvogel, Laurence [1 ,9 ,12 ,13 ]
Kroemer, Guido [1 ,2 ,3 ,4 ,5 ,11 ,32 ,33 ]
机构
[1] Gustave Roussy Canc Campus, Villejuif, France
[2] INSERM, U1138, Paris, France
[3] Ctr Rech Cordeliers, Equipe Labellisee Ligue Natl Canc 11, Paris, France
[4] Univ Paris 05, Sorbonne Paris Cite, Paris, France
[5] Univ Paris 06, Paris, France
[6] Suzhou Inst Syst Med, Suzhou, Jiangsu, Peoples R China
[7] Chinese Acad Med Sci, Beijing 100730, Peoples R China
[8] Peking Union Med Coll, Beijing 100021, Peoples R China
[9] Univ Paris Saclay, Fac Med, Le Kremlin Bicetre, France
[10] Regina Elena Inst Canc Res, Rome, Italy
[11] Gustave Roussy Canc Campus, Metabol & Cell Biol Platforms, Villejuif, France
[12] INSERM, U1015, Villejuif, France
[13] Ctr Clin Invest Biotherapies Canc CICBT 507, Villejuif, France
[14] Ist Super Sanita, Dept Hematol Oncol & Mol Med, I-00161 Rome, Italy
[15] Italian Natl Res Council, Inst Photon & Nanotechnol, Rome, Italy
[16] Univ Bonn, Life & Med Sci Ctr Inst, Genom & Immunoregulat, Bonn, Germany
[17] INSERM, U981, Villejuif, France
[18] Univ Paris Sorbonne Cite, UMRS 775, INSERM, Paris, France
[19] Ctr Ressources Biol CRB EPIGENETIC, INSERM, U1147, Paris, France
[20] Sotio, Prague, Czech Republic
[21] Ctr Georges Francois Leclerc, Dept Med Oncol, Dijon, France
[22] Univ Bourgogne Franche Comte, Dijon, France
[23] Ctr Georges Francois Leclerc, Dijon, France
[24] Univ Siena, Dept Life Sci, I-53100 Siena, Italy
[25] Hop La Pitie Salpetriere, Equipe Neurogenet & Physiol, Inst Cerveau & Moelle Epiniere, ICM,CNRS,UMR 7225,INSERM,U1127,UPMC P6,UMR S 1127, F-75013 Paris, France
[26] Gustave Roussy Canc Campus, Dept Med Oncol, Villejuif, France
[27] Gustave Roussy Canc Campus, Dept Breast Oncol, Villejuif, France
[28] Univ Franche Comte, INSERM 1098, F-25030 Besancon, France
[29] Gustave Roussy Canc Campus, Dept Biol & Pathol, Villejuif, France
[30] Gustave Roussy Canc Campus, Dept Med Oncol, Villejuif, France
[31] Univ Roma Tor Vergata, Dept Biol, I-00173 Rome, Italy
[32] Hop Europeen Georges Pompidou, AP HP, Pole Biol, Paris, France
[33] Karolinska Inst, Dept Womens & Childrens Hlth, Karolinska Univ Hosp, S-17176 Stockholm, Sweden
基金
欧洲研究理事会;
关键词
ANTIGEN-PRESENTING CELLS; ANTICANCER CHEMOTHERAPY; BREAST-CANCER; IMMUNOSURVEILLANCE; TUMOR; INFLAMMATION; RECRUITMENT; NEUTROPHILS; MECHANISM; THERAPY;
D O I
10.1126/science.aad0779
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Antitumor immunity driven by intratumoral dendritic cells contributes to the efficacy of anthracycline-based chemotherapy in cancer. We identified a loss-of-function allele of the gene coding for formyl peptide receptor 1 (FPR1) that was associated with poor metastasis-free and overall survival in breast and colorectal cancer patients receiving adjuvant chemotherapy. The therapeutic effects of anthracyclines were abrogated in tumor-bearing Fpr1(-/-) mice due to impaired antitumor immunity. Fpr1-deficient dendritic cells failed to approach dying cancer cells and, as a result, could not elicit antitumor T cell immunity. Experiments performed in a microfluidic device confirmed that FPR1 and its ligand, annexin-1, promoted stable interactions between dying cancer cells and human or murine leukocytes. Altogether, these results highlight the importance of FPR1 in chemotherapy-induced anticancer immune responses.
引用
收藏
页码:972 / 978
页数:7
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