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巨头联盟:CAR-T 细胞疗法与溶瘤病毒联合策略治疗血液系统恶性肿瘤。

Alliance between titans: combination strategies of CAR-T cell therapy and oncolytic virus for the treatment of hematological malignancies.

机构信息

Emergency, Tianjin First Central Hospital, Tianjin, 300192, China.

First Center Clinic College of Tianjin Medical University, Tianjin, 300192, China.

出版信息

Ann Hematol. 2024 Aug;103(8):2569-2589. doi: 10.1007/s00277-023-05488-9. Epub 2023 Oct 18.


DOI:10.1007/s00277-023-05488-9
PMID:37853078
Abstract

There have been several clinical studies using chimeric antigen receptor (CAR)-T cell therapy for different hematological malignancies. It has transformed the therapy landscape for hematologic malignancies dramatically. Nonetheless, in acute myeloid leukemia (AML) and T cell malignancies, it still has a dismal prognosis. Even in the most promising locations, recurrence with CAR-T treatment remains a big concern. Oncolytic viruses (OVs) can directly lyse tumor cells or cause immune responses, and they can be manipulated to create therapeutic proteins, increasing anticancer efficacy. Oncolytic viruses have been proven in a rising number of studies to be beneficial in hematological malignancies. There are limitations that cannot be avoided by using either treatment alone, and the combination of CAR-T cell therapy and oncolytic virus therapy may complement the disadvantages of individual application, enhance the advantages of their respective treatment methods and improve the treatment effect. The alternatives for combining two therapies in hematological malignancies are discussed in this article.

摘要

已经有几项使用嵌合抗原受体(CAR)-T 细胞疗法治疗不同血液系统恶性肿瘤的临床研究。它极大地改变了血液系统恶性肿瘤的治疗格局。然而,在急性髓系白血病(AML)和 T 细胞恶性肿瘤中,它的预后仍然很差。即使在最有希望的部位,CAR-T 治疗后的复发仍然是一个大问题。溶瘤病毒(OV)可以直接裂解肿瘤细胞或引起免疫反应,并且可以对其进行改造以产生治疗性蛋白,从而提高抗癌疗效。越来越多的研究已经证明溶瘤病毒对血液系统恶性肿瘤有益。这两种治疗方法单独使用都有无法避免的局限性,CAR-T 细胞疗法和溶瘤病毒疗法的联合应用可能可以互补各自应用的缺点,增强各自治疗方法的优势,提高治疗效果。本文讨论了血液系统恶性肿瘤中联合两种疗法的选择。

相似文献

[1]
Alliance between titans: combination strategies of CAR-T cell therapy and oncolytic virus for the treatment of hematological malignancies.

Ann Hematol. 2024-8

[2]
Oncolytic viruses as a promising therapeutic strategy for hematological malignancies.

Biomed Pharmacother. 2021-7

[3]
Tumor-tagging by oncolytic viruses: A novel strategy for CAR-T therapy against solid tumors.

Cancer Lett. 2021-4-10

[4]
Therapeutic potential of CAR T cell in malignancies: A scoping review.

Biomed Pharmacother. 2022-2

[5]
Clinical CAR-T Cell and Oncolytic Virotherapy for Cancer Treatment.

Mol Ther. 2021-2-3

[6]
Combining Oncolytic Viruses with Chimeric Antigen Receptor T Cell Therapy.

Hum Gene Ther. 2021-2

[7]
CAR T-Cell Therapy in Hematological Malignancies.

Int J Mol Sci. 2021-8-20

[8]
Synergistic combination of oncolytic virotherapy with CAR T-cell therapy.

Prog Mol Biol Transl Sci. 2019-7-19

[9]
Pancreatic cancer therapy with combined mesothelin-redirected chimeric antigen receptor T cells and cytokine-armed oncolytic adenoviruses.

JCI Insight. 2018-4-5

[10]
[Combination of Oncolytic Virotherapy and CAR T/NK Cell Therapy for the Treatment of Cancer].

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引用本文的文献

[1]
Strategies to overcome tumour relapse caused by antigen escape after CAR T therapy.

Mol Cancer. 2025-4-28

[2]
Mesenchymal Stem-Cell-Derived Exosomes as Novel Drug Carriers in Anti-Cancer Treatment: A Myth or Reality?

Cells. 2025-1-29

[3]
The Bidirectional Interplay between T Cell-Based Immunotherapies and the Tumor Microenvironment.

Cancer Immunol Res. 2025-4-2

[4]
Overcoming Antigen Escape and T-Cell Exhaustion in CAR-T Therapy for Leukemia.

Cells. 2024-9-23

[5]
Broadening the horizon: potential applications of CAR-T cells beyond current indications.

Front Immunol. 2023

本文引用的文献

[1]
SARS-CoV-2 as an Oncolytic Virus Following Reactivation of the Immune System: A Review.

Int J Mol Sci. 2023-1-24

[2]
Exploring the Interactions of Oncolytic Viral Therapy and Immunotherapy of Anti-CTLA-4 for Malignant Melanoma Mice Model.

Cells. 2023-2-3

[3]
CXCL11-armed oncolytic adenoviruses enhance CAR-T cell therapeutic efficacy and reprogram tumor microenvironment in glioblastoma.

Mol Ther. 2023-1-4

[4]
Non-viral, specifically targeted CAR-T cells achieve high safety and efficacy in B-NHL.

Nature. 2022-9

[5]
Induction of tumor cell autosis by myxoma virus-infected CAR-T and TCR-T cells to overcome primary and acquired resistance.

Cancer Cell. 2022-9-12

[6]
Remodeling the tumor microenvironment by oncolytic viruses: beyond oncolysis of tumor cells for cancer treatment.

J Immunother Cancer. 2022-5

[7]
A combination therapy of oncolytic viruses and chimeric antigen receptor T cells: a mathematical model proof-of-concept.

Math Biosci Eng. 2022-3-2

[8]
Oncolytic virus-mediated expansion of dual-specific CAR T cells improves efficacy against solid tumors in mice.

Sci Transl Med. 2022-4-13

[9]
Clinical activity of single-dose systemic oncolytic VSV virotherapy in patients with relapsed refractory T-cell lymphoma.

Blood Adv. 2022-6-14

[10]
Decade-long leukaemia remissions with persistence of CD4 CAR T cells.

Nature. 2022-2

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