Type I interferons in anticancer immunity

被引:1005
作者
Zitvogel, Laurence [1 ,2 ,3 ,4 ]
Galluzzi, Lorenzo [1 ,5 ,6 ,7 ,8 ]
Kepp, Oliver [5 ,6 ,7 ,8 ]
Smyth, Mark J. [11 ,12 ]
Kroemer, Guido [5 ,6 ,7 ,8 ,9 ,10 ,13 ]
机构
[1] Gustave Roussy Canc Campus, Villejuif, France
[2] INSERM, U1015, F-94800 Villejuif, France
[3] Univ Paris 11, Fac Med, F-94270 Le Kremlin Bicetre, France
[4] Ctr Clin Invest Biotherapies Canc CICBT 507, F-94800 Villejuif, France
[5] Ctr Rech Cordeliers, Equipe Labellisee Ligue Natl Canc 11, F-75006 Paris, France
[6] INSERM, U1138, F-75006 Paris, France
[7] Univ Paris 06, F-75006 Paris, France
[8] Univ Paris 06, F-75006 Paris, France
[9] Gustave Roussy Canc Campus, Metabol Platform, F-94800 Villejuif, France
[10] Gustave Roussy Canc Campus, Cell Biol Platform, F-94800 Villejuif, France
[11] Queensland Inst Med Res, Immunol Canc & Infect Lab, Berghofer Med Res Inst, Herston, Qld 4006, Australia
[12] Univ Queensland, Sch Med, Herston, Qld 4006, Australia
[13] Hop Europeen Georges Pompidou, F-75015 Paris, France
基金
英国医学研究理事会; 欧洲研究理事会;
关键词
DENDRITIC CELL-RECEPTOR; IFN-ALPHA; T-CELLS; PEGYLATED INTERFERON-ALPHA-2B; MOLECULAR RESPONSE; ADAPTIVE IMMUNITY; ADJUVANT THERAPY; STEM-CELLS; CANCER; INNATE;
D O I
10.1038/nri3845
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Type I interferons (IFNs) are known for their key role in antiviral immune responses. In this Review, we discuss accumulating evidence indicating that type I IFNs produced by malignant cells or tumour-infiltrating dendritic cells also control the autocrine or paracrine circuits that underlie cancer immunosurveillance. Many conventional chemotherapeutics, targeted anticancer agents, immunological adjuvants and oncolytic viruses are only fully efficient in the presence of intact type I IFN signalling. Moreover, the intratumoural expression levels of type I IFNs or of IFN-stimulated genes correlate with favourable disease outcome in several cohorts of patients with cancer. Finally, new anticancer immunotherapies are being developed that are based on recombinant type I IFNs, type I IFN-encoding vectors and type I IFN-expressing cells.
引用
收藏
页码:405 / 414
页数:10
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