Tumor-infiltrating lymphocytes for adoptive cell therapy: recent advances, challenges, and future directions

被引:37
|
作者
Granhoj, Joachim Stoltenborg [1 ]
Jensen, Agnete Witness Praest [1 ]
Presti, Mario [1 ]
Met, Ozcan [1 ]
Svane, Inge Marie [1 ]
Donia, Marco [1 ]
机构
[1] Copenhagen Univ Hosp, Natl Ctr Canc Immune Therapy CCIT DK, Dept Oncol, Herlev, Denmark
关键词
Adoptive cell therapy; cellular immunotherapy; cell therapy; resistance to immunotherapy; tumor-infiltrating lymphocytes; TILs; CD8(+) T-CELLS; AMINO-ACID-TRANSPORT; METASTATIC MELANOMA; ACQUIRED-RESISTANCE; METABOLIC-REGULATION; COMPLETE RESPONSES; CANCER REGRESSION; IMMUNE RESISTANCE; SUPPRESSOR-CELLS; PROGNOSTIC VALUE;
D O I
10.1080/14712598.2022.2064711
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction Adoptive cell therapy (ACT) with tumor-infiltrating lymphocytes (TILs) is a highly personalized type of cancer immunotherapy. TIL-based ACT exploits naturally occurring TILs, derived from the patients' tumor. This treatment has shown consistent clinical responses in melanoma, and recent results point toward a potential use in multiple cancer diagnoses. However, several limitations have restricted the clinical development and adaptation of TIL-based ACT. Areas covered In this review, we present the principles of TIL-based ACT and discuss the most significant limitations for therapeutic efficacy and its widespread application. The topics of therapeutic resistance (both innate and acquired), treatment-related toxicity, and the novel research topic of metabolic barriers in the tumor microenvironment (TME) are covered. Expert opinion There are many ongoing areas of research focusing on improving clinical efficacy and optimizing TIL-based ACT. Many strategies have shown a great potential, particularly strategies advancing TIL efficacy (such as increasing and harnessing ex vivo the sub-population of tumor-reactive TILs) and manufacturing processes. Novel approaches can help overcome current limitations and potentially result in TIL-based ACT entering the mainstream of cancer therapy across tumor types.
引用
收藏
页码:627 / 641
页数:15
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