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Immune evasion in cell-based immunotherapy: unraveling challenges and novel strategies
被引:19
|作者:
Li, Yan-Ruide
[1
]
Halladay, Tyler
[1
]
Yang, Lili
[1
,2
,3
,4
]
机构:
[1] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell R, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Mol Biol Inst, Los Angeles, CA 90095 USA
关键词:
Immune evasion;
Cell-based immunotherapies (CBIs);
Chimeric antigen receptor (CAR);
CAR-engineered T (CAR-T) cell therapy;
Tumor microenvironment (TME);
Immune checkpoint proteins;
Tumor heterogeneity;
CAR-T-CELLS;
MHC CLASS-I;
ACUTE LYMPHOBLASTIC-LEUKEMIA;
B-CELL;
ADENOSINE RECEPTORS;
CHECKPOINT BLOCKADE;
ANTITUMOR-ACTIVITY;
HUMAN-LYMPHOCYTES;
UP-REGULATION;
TUMOR-CELLS;
D O I:
10.1186/s12929-024-00998-8
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Cell-based immunotherapies (CBIs), notably exemplified by chimeric antigen receptor (CAR)-engineered T (CAR-T) cell therapy, have emerged as groundbreaking approaches for cancer therapy. Nevertheless, akin to various other therapeutic modalities, tumor cells employ counterstrategies to manifest immune evasion, thereby circumventing the impact of CBIs. This phenomenon is facilitated by an intricately immunosuppression entrenched within the tumor microenvironment (TME). Principal mechanisms underpinning tumor immune evasion from CBIs encompass loss of antigens, downregulation of antigen presentation, activation of immune checkpoint pathways, initiation of anti-apoptotic cascades, and induction of immune dysfunction and exhaustion. In this review, we delve into the intrinsic mechanisms underlying the capacity of tumor cells to resist CBIs and proffer prospective stratagems to navigate around these challenges.
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页数:16
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