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

被引:18
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.
引用
收藏
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
    Abiko, K.
    Matsumura, N.
    Hamanishi, J.
    Horikawa, N.
    Murakami, R.
    Yamaguchi, K.
    Yoshioka, Y.
    Baba, T.
    Konishi, I.
    Mandai, M.
    [J]. 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
    Banna, Giuseppe Luigi
    Passiglia, Francesco
    Colonese, Francesca
    Canova, Stefania
    Menis, Jessica
    Addeo, Alfredo
    Russo, Antonio
    Cortinovis, Diego Luigi
    [J]. CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2018, 129 : 27 - 39
  • [3] Proteomic analysis of exosomes isolated from human malignant pleural effusions
    Bard, MP
    Hegmans, JP
    Hemmes, A
    Luider, TM
    Willemsen, R
    Severijnen, LAA
    van Meerbeeck, JP
    Burgers, SA
    Hoogsteden, HC
    Lambrecht, BN
    [J]. 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
    Bardhan, Kankana
    Anagnostou, Theodora
    Boussiotis, Vassiliki A.
    [J]. FRONTIERS IN IMMUNOLOGY, 2016, 7
  • [5] PD-L1 blockade engages tumor-infiltrating lymphocytes to co-express targetable activating and inhibitory receptors
    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
    [J]. 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
    Boussiotis, VA
    Freeman, GJ
    Taylor, PA
    Berezovskaya, A
    Grass, I
    Blazar, BR
    Nadler, LM
    [J]. NATURE MEDICINE, 2000, 6 (03) : 290 - 297
  • [7] Exosomal-like vesicles are present in human blood plasma
    Caby, MP
    Lankar, D
    Vincendeau-Scherrer, C
    Raposo, G
    Bonnerot, C
    [J]. 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
    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
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (02) : 457 - 471
  • [9] Exosomal PD-L1 contributes to immunosuppression and is associated with anti-PD-1 response
    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
    [J]. NATURE, 2018, 560 (7718) : 382 - +
  • [10] Human tumor-derived exosomes selectively impair lymphocyte responses to interieukin-2
    Clayton, Aled
    Mitchell, J. Paul
    Court, Jacquelyn
    Mason, Malcolm D.
    Tabi, Zsuzsanna
    [J]. CANCER RESEARCH, 2007, 67 (15) : 7458 - 7466