Directing CAR T cells towards the tumor vasculature for the treatment of solid tumors

被引:30
作者
Akbari, Parvin [1 ]
Katsarou, Afroditi [1 ]
Daghighian, Roxanna [1 ]
van Mil, Lotte W. H. G. [1 ]
Huijbers, Elisabeth J. M. [1 ]
Griffioen, Arjan W. [1 ]
van Beijnum, Judy R. [1 ]
机构
[1] Vrije Univ Amsterdam, Canc Ctr Amsterdam, Dept Med Oncol, Amsterdam UMC,Angiogenesis Lab, Amsterdam, Netherlands
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2022年 / 1877卷 / 03期
关键词
Cancer; CAR T cell; Immune suppression; Tumor microenvironment; Angiogenesis; CHIMERIC ANTIGEN RECEPTOR; INDOLEAMINE 2,3-DIOXYGENASE; GENE-EXPRESSION; CANCER REGRESSION; IMMUNOTHERAPY; ANGIOGENESIS; LYMPHOCYTES; AFFINITY; THERAPY; RECOGNITION;
D O I
10.1016/j.bbcan.2022.188701
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
For successful application of chimeric antigen receptor (CAR) T cell therapy in solid tumors, major hurdles have to be overcome. CAR T cells have to cross the vascular barrier, which is hampered by the anergic state of the tumor vasculature, characterized by suppressed levels of leukocyte adhesion molecules on the endothelium. Additional immunosuppressive mechanisms in the solid tumor microenvironment can affect infiltration, activity and persistence of CAR T cells. Redirecting CAR T cells towards the tumor vasculature poses a possible solution, as molecular targets of tumor endothelial cells can be directly engaged from within the blood.In this review, we discuss recent advances in CAR T cell therapy against solid tumors, with a focus on targeting the tumor vasculature. Furthermore, we discuss opportunities to overcome challenges and barriers through engineering of CAR T cells to enhance trafficking, safety and efficacy.
引用
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页数:11
相关论文
共 127 条
[1]   The tumor vasculature an attractive CAR T cell target in solid tumors [J].
Akbari, Parvin ;
Huijbers, Elisabeth J. M. ;
Themeli, Maria ;
Griffioen, Arjan W. ;
van Beijnum, Judy R. .
ANGIOGENESIS, 2019, 22 (04) :473-475
[2]   Obstacles Posed by the Tumor Microenvironment to T cell Activity: A Case for Synergistic Therapies [J].
Anderson, Kristin G. ;
Stromnes, Ingunn M. ;
Greenberg, Philip D. .
CANCER CELL, 2017, 31 (03) :311-325
[3]   Bevacizumab-mediated tumor vasculature remodelling improves tumor infiltration and antitumor efficacy of GD2-CAR T cells in a human neuroblastoma preclinical model [J].
Bocca, Paola ;
Di Carlo, Emma ;
Caruana, Ignazio ;
Emionite, Laura ;
Cilli, Michele ;
De Angelis, Biagio ;
Quintarelli, Concetta ;
Pezzolo, Annalisa ;
Raffaghello, Lizzia ;
Morandi, Fabio ;
Locatelli, Franco ;
Pistoia, Vito ;
Prigione, Ignazia .
ONCOIMMUNOLOGY, 2018, 7 (01)
[4]   In the Eye of the Storm: Immune-mediated Toxicities Associated With CAR-T Cell Therapy [J].
Borrega, Jorge Garcia ;
Goedel, Philipp ;
Rueger, Maria Adele ;
Onur, Oezguer A. ;
Shimabukuro-Vornhagen, Alexander ;
Kochanek, Matthias ;
Boell, Boris .
HEMASPHERE, 2019, 3 (02)
[5]   SIGNALS THROUGH T-CELL RECEPTOR-ZETA CHAIN ALONE ARE INSUFFICIENT TO PRIME RESTING T-LYMPHOCYTES [J].
BROCKER, T ;
KARJALAINEN, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (05) :1653-1659
[6]   TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer [J].
Byrd, Tiara T. ;
Fousek, Kristen ;
Pignata, Antonella ;
Szot, Christopher ;
Samaha, Heba ;
Seaman, Steven ;
Dobrolecki, Lacey ;
Salsman, Vita S. ;
Oo, Htoo Zarni ;
Bielamowicz, Kevin ;
Landi, Daniel ;
Rainusso, Nino ;
Hicks, John ;
Powell, Suzanne ;
Baker, Matthew L. ;
Wels, Winfried S. ;
Koch, Joachim ;
Sorensen, Poul H. ;
Deneen, Benjamin ;
Ellis, Matthew J. ;
Lewis, Michael T. ;
Hegde, Meenakshi ;
Fletcher, Bradley S. ;
St Croix, Brad ;
Ahmed, Nabil .
CANCER RESEARCH, 2018, 78 (02) :489-500
[7]  
CAR, T CELL REC IMM TARG
[8]  
Carson-Walter EB, 2001, CANCER RES, V61, P6649
[9]   Tuning Sensitivity of CAR to EGFR Density Limits Recognition of Normal Tissue While Maintaining Potent Antitumor Activity [J].
Caruso, Hillary G. ;
Hurton, Lenka V. ;
Najjar, Amer ;
Rushworth, David ;
Ang, Sonny ;
Olivares, Simon ;
Mi, Tiejuan ;
Switzer, Kirsten ;
Singh, Harjeet ;
Huls, Helen ;
Lee, Dean A. ;
Heimberger, Amy B. ;
Champlin, Richard E. ;
Cooper, Laurence J. N. .
CANCER RESEARCH, 2015, 75 (17) :3505-3518
[10]   Tumor regression and immunity in combination therapy with anti-CEA chimeric antigen receptor T cells and anti-CEA-IL2 immunocytokine [J].
Cha, Seung E. ;
Kujawski, Maciej ;
J. Yazaki, Paul ;
Brown, Christine ;
Shively, John E. .
ONCOIMMUNOLOGY, 2021, 10 (01)