Neutrophil diversity and plasticity in tumour progression and therapy

被引:799
作者
Jaillon, Sebastien [1 ,2 ]
Ponzetta, Andrea [1 ,2 ]
Di Mitri, Diletta [2 ]
Santoni, Angela [3 ,4 ]
Bonecchi, Raffaella [1 ,2 ]
Mantovani, Alberto [1 ,2 ,5 ]
机构
[1] Humanitas Univ, Dept Biomed Sci, Pieve Emanuele, MI, Italy
[2] Humanitas Clin & Res Ctr IRCCS, Rozzano, MI, Italy
[3] Univ Roma La Sapienza, Fdn Cenci Bolognetti, Dipartimento Med Mol, Ist Pasteur, Rome, Italy
[4] IRCCS Neuromed, Pozzilli, IS, Italy
[5] Queen Mary Univ London, William Harvey Res Inst, London, England
关键词
TO-LYMPHOCYTE RATIO; COLONY-STIMULATING FACTOR; EXTRACELLULAR TRAPS PROMOTE; NIVOLUMAB-TREATED PATIENTS; REDUCED CLINICAL BENEFIT; RENAL-CELL CARCINOMA; ANTI-VEGF THERAPY; G-CSF; BONE-MARROW; SUPPRESSOR-CELLS;
D O I
10.1038/s41568-020-0281-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Neutrophils play a key role in defence against infection and in the activation and regulation of innate and adaptive immunity. In cancer, tumour-associated neutrophils (TANs) have emerged as an important component of the tumour microenvironment. Here, they can exert dual functions. TANs can be part of tumour-promoting inflammation by driving angiogenesis, extracellular matrix remodelling, metastasis and immunosuppression. Conversely, neutrophils can also mediate antitumour responses by direct killing of tumour cells and by participating in cellular networks that mediate antitumour resistance. Neutrophil diversity and plasticity underlie the dual potential of TANs in the tumour microenvironment. Myeloid checkpoints as well as the tumour and tissue contexture shape neutrophil function in response to conventional therapies and immunotherapy. We surmise that neutrophils can provide tools to tailor current immunotherapy strategies and pave the way to myeloid cell-centred therapeutic strategies, which would be complementary to current approaches. This Review discusses the emerging dual role played by neutrophils in the tumour microenvironment as part of tumour-promoting inflammation, while also mediating antitumour immune responses, and suggests that neutrophil function could be manipulated in myeloid cell-based therapeutic approaches to improve patient outcomes.
引用
收藏
页码:485 / 503
页数:19
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