Blood-based PD-L1 analysis in tumor-derived extracellular vesicles: Applications for optimal use of anti-PD-1/PD-L1 axis inhibitors

被引:17
作者
Del Re, Marzia [1 ]
van Schaik, Ron Hn [2 ]
Fogli, Stefano [1 ]
Mathijssen, Ron Hj [3 ]
Cucchiara, Federico [1 ]
Capuano, Annalisa [4 ]
Scavone, Cristina [4 ]
Jenster, Guido W. [5 ]
Danesi, Romano [1 ]
机构
[1] Univ Pisa, Dept Clin & Expt Med, Unit Clin Pharmacol & Pharmacogenet, 55 Via Roma, I-56126 Pisa, Italy
[2] Erasmus MC, Dept Clin Chem, Rotterdam, Netherlands
[3] Erasmus MC Canc Inst, Dept Med Oncol, Rotterdam, Netherlands
[4] Univ Campania Luigi Vanvitelli, Dept Expt Med, Naples, Italy
[5] Erasmus MC Canc Inst, Dept Urol, Rotterdam, Netherlands
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2021年 / 1875卷 / 01期
关键词
Extracellular vesicles; Exosomes; PD-1/PD-L1; Liquid biopsy; Cancer; Immune-checkpoint inhibitors; EXOSOMES; CANCER; EXPRESSION; PLASMA; PROSTASOMES; SUPPRESSION; ACTIVATION; MECHANISMS; MATURATION; BIOMARKER;
D O I
10.1016/j.bbcan.2020.188463
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Monoclonal antibodies that inhibit the programmed cell death protein 1 axis (anti-PD-1/PD-L1) are part of a new pharmacological strategy aimed at reinforcing the immune response to cancer. Despite the success in several cancer types, a significant percentage of patients do not benefit from treatment with these drugs due to intrinsic or acquired resistance or the occurrence of immune-related adverse reactions. Assessment of PD-L1 expression in tumor tissues is currently used to predict drug response in the clinics; however, there is a growing interest in identifying blood-based biomarkers that, owing to the minimally-invasive nature, can allow a dynamic monitoring of drug response in daily clinical practice. In the current review article, we discuss whether the assessment of PD-L1 mRNA and protein levels in circulating extracellular vesicles may have the potential to predict the likelihood of tumor response to anti-PD-1/PD-L1 antibodies.
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页数:9
相关论文
共 84 条
[1]   IFN-γ from lymphocytes induces PD-L1 expression and promotes progression of ovarian cancer [J].
Abiko, K. ;
Matsumura, N. ;
Hamanishi, J. ;
Horikawa, N. ;
Murakami, R. ;
Yamaguchi, K. ;
Yoshioka, Y. ;
Baba, T. ;
Konishi, I. ;
Mandai, M. .
BRITISH JOURNAL OF CANCER, 2015, 112 (09) :1501-1509
[2]   Immune-checkpoint inhibitors in non-small cell lung cancer: A tool to improve patients' selection [J].
Banna, Giuseppe Luigi ;
Passiglia, Francesco ;
Colonese, Francesca ;
Canova, Stefania ;
Menis, Jessica ;
Addeo, Alfredo ;
Russo, Antonio ;
Cortinovis, Diego Luigi .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2018, 129 :27-39
[3]   Proteomic analysis of exosomes isolated from human malignant pleural effusions [J].
Bard, MP ;
Hegmans, JP ;
Hemmes, A ;
Luider, TM ;
Willemsen, R ;
Severijnen, LAA ;
van Meerbeeck, JP ;
Burgers, SA ;
Hoogsteden, HC ;
Lambrecht, BN .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2004, 31 (01) :114-121
[4]   The PD1:PD-L1/2 Pathway from Discovery to Clinical implementation [J].
Bardhan, Kankana ;
Anagnostou, Theodora ;
Boussiotis, Vassiliki A. .
FRONTIERS IN IMMUNOLOGY, 2016, 7
[5]   PD-L1 blockade engages tumor-infiltrating lymphocytes to co-express targetable activating and inhibitory receptors [J].
Beyrend, Guillaume ;
van der Gracht, Esme ;
Yilmaz, Ayse ;
van Duikeren, Suzanne ;
Camps, Marcel ;
Hollt, Thomas ;
Vilanova, Anna ;
van Unen, Vincent ;
Koning, Frits ;
de Miranda, Noel F. C. C. ;
Arens, Ramon ;
Ossendorp, Ferry .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2019, 7 (01)
[6]   p27kip1 functions as an anergy factor inhibiting interleukin 2 transcription and clonal expansion of alloreactive human and mouse helper T lymphocytes [J].
Boussiotis, VA ;
Freeman, GJ ;
Taylor, PA ;
Berezovskaya, A ;
Grass, I ;
Blazar, BR ;
Nadler, LM .
NATURE MEDICINE, 2000, 6 (03) :290-297
[7]   Exosomal-like vesicles are present in human blood plasma [J].
Caby, MP ;
Lankar, D ;
Vincendeau-Scherrer, C ;
Raposo, G ;
Bonnerot, C .
INTERNATIONAL IMMUNOLOGY, 2005, 17 (07) :879-887
[8]   Membrane-associated Hsp72 from tumor-derived exosomes mediates STAT3-dependent immunosuppressive function of mouse and human myeloid-derived suppressor cells [J].
Chalmin, Fanny ;
Ladoire, Sylvain ;
Mignot, Gregoire ;
Vincent, Julie ;
Bruchard, Melanie ;
Remy-Martin, Jean-Paul ;
Boireau, Wilfrid ;
Rouleau, Alain ;
Simon, Benoit ;
Lanneau, David ;
De Thonel, Aurelie ;
Multhoff, Gabriele ;
Hamman, Arlette ;
Martin, Francois ;
Chauffert, Bruno ;
Solary, Eric ;
Zitvogel, Laurence ;
Garrido, Carmen ;
Ryffel, Bernhard ;
Borg, Christophe ;
Apetoh, Lionel ;
Rebe, Cedric ;
Ghiringhelli, Francois .
JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (02) :457-471
[9]   Exosomal PD-L1 contributes to immunosuppression and is associated with anti-PD-1 response [J].
Chen, Gang ;
Huang, Alexander C. ;
Zhang, Wei ;
Zhang, Gao ;
Wu, Min ;
Xu, Wei ;
Yu, Zili ;
Yang, Jiegang ;
Wang, Beike ;
Sun, Honghong ;
Xia, Houfu ;
Man, Qiwen ;
Zhong, Wenqun ;
Antelo, Leonardo F. ;
Wu, Bin ;
Xiong, Xuepeng ;
Liu, Xiaoming ;
Guan, Lei ;
Li, Ting ;
Liu, Shujing ;
Yang, Ruifeng ;
Lu, Youtao ;
Dong, Liyun ;
McGettigan, Suzanne ;
Somasundaram, Rajasekharan ;
Radhakrishnan, Ravi ;
Mills, Gordon ;
Lu, Yiling ;
Kim, Junhyong ;
Chen, Youhai H. ;
Dong, Haidong ;
Zhao, Yifang ;
Karakousis, Giorgos C. ;
Mitchell, Tara C. ;
Schuchter, Lynn M. ;
Herlyn, Meenhard ;
Wherry, E. John ;
Xu, Xiaowei ;
Guo, Wei .
NATURE, 2018, 560 (7718) :382-+
[10]   Human tumor-derived exosomes selectively impair lymphocyte responses to interieukin-2 [J].
Clayton, Aled ;
Mitchell, J. Paul ;
Court, Jacquelyn ;
Mason, Malcolm D. ;
Tabi, Zsuzsanna .
CANCER RESEARCH, 2007, 67 (15) :7458-7466