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预测 CAR T 疗法疗效的生物标志物:现状与未来展望。

Biomarkers for prediction of CAR T therapy outcomes: current and future perspectives.

机构信息

Institute of Microbiology and Immunology, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.

出版信息

Front Immunol. 2024 Mar 15;15:1378944. doi: 10.3389/fimmu.2024.1378944. eCollection 2024.


DOI:10.3389/fimmu.2024.1378944
PMID:38558801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10979304/
Abstract

Chimeric antigen receptor (CAR) T cell therapy holds enormous potential for the treatment of hematologic malignancies. Despite its benefits, it is still used as a second line of therapy, mainly because of its severe side effects and patient unresponsiveness. Numerous researchers worldwide have attempted to identify effective predictive biomarkers for early prediction of treatment outcomes and adverse effects in CAR T cell therapy, albeit so far only with limited success. This review provides a comprehensive overview of the current state of predictive biomarkers. Although existing predictive metrics correlate to some extent with treatment outcomes, they fail to encapsulate the complexity of the immune system dynamics. The aim of this review is to identify six major groups of predictive biomarkers and propose their use in developing improved and efficient prediction models. These groups include changes in mitochondrial dynamics, endothelial activation, central nervous system impairment, immune system markers, extracellular vesicles, and the inhibitory tumor microenvironment. A comprehensive understanding of the multiple factors that influence therapeutic efficacy has the potential to significantly improve the course of CAR T cell therapy and patient care, thereby making this advanced immunotherapy more appealing and the course of therapy more convenient and favorable for patients.

摘要

嵌合抗原受体 (CAR) T 细胞疗法在治疗血液系统恶性肿瘤方面具有巨大潜力。尽管有其益处,但它仍被用作二线治疗,主要是因为其严重的副作用和患者无反应性。世界各地的许多研究人员都试图确定有效的预测生物标志物,以便早期预测 CAR T 细胞治疗的治疗结果和不良反应,但迄今为止,仅取得了有限的成功。本综述全面概述了当前预测生物标志物的状况。尽管现有的预测指标在某种程度上与治疗结果相关,但它们未能涵盖免疫系统动态的复杂性。本综述的目的是确定六大类预测生物标志物,并提出将其用于开发改进和有效的预测模型。这些组包括线粒体动力学的变化、内皮细胞激活、中枢神经系统损伤、免疫系统标志物、细胞外囊泡和抑制性肿瘤微环境。全面了解影响治疗效果的多种因素有可能显著改善 CAR T 细胞治疗和患者护理的进程,从而使这种先进的免疫疗法更具吸引力,治疗过程更方便、更有利于患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522e/10979304/93450c377186/fimmu-15-1378944-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522e/10979304/27cc9a45f44e/fimmu-15-1378944-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522e/10979304/52b0089a7243/fimmu-15-1378944-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522e/10979304/40a931bf3f74/fimmu-15-1378944-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522e/10979304/93450c377186/fimmu-15-1378944-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522e/10979304/27cc9a45f44e/fimmu-15-1378944-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522e/10979304/52b0089a7243/fimmu-15-1378944-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522e/10979304/40a931bf3f74/fimmu-15-1378944-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522e/10979304/93450c377186/fimmu-15-1378944-g004.jpg

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Biomarkers for prediction of CAR T therapy outcomes: current and future perspectives.

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NPJ Digit Med. 2025-8-1

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CAR T-cell therapy in hematologic and solid malignancies: mechanisms, clinical applications, and future directions.

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[4]
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[5]
Cytokine release syndrome and CAR T Cell therapy: Modulating the intensity of the inflammatory response and resolution within the tumor microenvironment.

Front Pharmacol. 2025-6-10

[6]
Cord blood-derived iNK T cells as a platform for allogeneic CAR T cell therapy.

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[7]
Radiomic Features Prognosticate Treatment Response in CAR-T Cell Therapy.

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[8]
An Analysis of Monitoring Solutions for CAR T Cell Production.

Healthc Technol Lett. 2025-5-13

[9]
European survey on CAR T-Cell analytical methods from apheresis to post-infusion immunomonitoring.

Front Immunol. 2025-4-24

[10]
State of the art in CAR-based therapy: In vivo CAR production as a revolution in cell-based cancer treatment.

Cell Oncol (Dordr). 2025-4-22

本文引用的文献

[1]
A Novel and Validated Inflammation-Based Prognosis Score (IBPS) Predicts Outcomes in Patients with Diffuse Large B-Cell Lymphoma.

Cancer Manag Res. 2023-7-13

[2]
Comorbidities in DLBCL: too "Severe4" CAR-T therapy?

Blood Adv. 2023-7-25

[3]
Omics approaches for the assessment of biological responses to nanoparticles.

Adv Drug Deliv Rev. 2023-9

[4]
Site-specific transgene integration in chimeric antigen receptor (CAR) T cell therapies.

Biomark Res. 2023-7-4

[5]
A combination of pre-infusion serum ferritin, CRP and IL-6 predicts outcome in relapsed/refractory multiple myeloma patients treated with CAR-T cells.

Front Immunol. 2023

[6]
Characterization of the endotheliopathy, innate-immune activation and hemostatic imbalance underlying CAR-T cell toxicities: laboratory tools for an early and differential diagnosis.

J Immunother Cancer. 2023-4

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CAR-T-Derived Extracellular Vesicles: A Promising Development of CAR-T Anti-Tumor Therapy.

Cancers (Basel). 2023-2-7

[8]
Vagal Nerve Activity Predicts Prognosis in Diffused Large B-Cell Lymphoma and Multiple Myeloma.

J Clin Med. 2023-1-23

[9]
A validated composite comorbidity index predicts outcomes of CAR T-cell therapy in patients with diffuse large B-cell lymphoma.

Blood Adv. 2023-7-25

[10]
Editorial: Immune modulation in tumor microenvironment: New perspectives for cancer immunotherapy.

Front Cell Dev Biol. 2023-1-4

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