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基于NKG2D的嵌合抗原受体(CAR)当前临床试验综述。

A summary of current NKG2D-based CAR clinical trials.

作者信息

Curio Sophie, Jonsson Gustav, Marinović Sonja

机构信息

Department of Life Sciences, Imperial College London, London, UK.

The University of Queensland Diamantina Institute, The University of Queensland, Woolloongabba, QLD 4102, Australia.

出版信息

Immunother Adv. 2021 Aug 13;1(1):ltab018. doi: 10.1093/immadv/ltab018. eCollection 2021 Jan.


DOI:10.1093/immadv/ltab018
PMID:34604863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8480431/
Abstract

Cancer immunotherapies have significantly improved patient survival and treatment options in recent years. Nonetheless, the success of immunotherapy is limited to certain cancer types and specific subgroups of patients, making the development of new therapeutic approaches a topic of ongoing research. Chimeric antigen receptor (CAR) cells are engineered immune cells that are programmed to specifically eliminate cancer cells. Ideally, a CAR recognizes antigens that are restricted to tumor cells to avoid off-target effects. NKG2D is an activating immunoreceptor and an important player in anti-tumor immunity due to its ability to recognize tumor cells and initiate an anti-tumor immune response. Ligands for NKG2D are expressed on malignant or stressed cells and typically absent from healthy tissue, making it a promising CAR candidate. Here, we provide a summary of past and ongoing NKG2D-based CAR clinical trials and comment on potential pitfalls.

摘要

近年来,癌症免疫疗法显著提高了患者的生存率并增加了治疗选择。尽管如此,免疫疗法的成功仅限于某些癌症类型和特定患者亚组,这使得开发新的治疗方法成为一个持续研究的课题。嵌合抗原受体(CAR)细胞是经过工程改造的免疫细胞,被编程为特异性消除癌细胞。理想情况下,CAR识别仅限于肿瘤细胞的抗原以避免脱靶效应。NKG2D是一种激活型免疫受体,由于其能够识别肿瘤细胞并启动抗肿瘤免疫反应,因此是抗肿瘤免疫中的重要参与者。NKG2D的配体在恶性或应激细胞上表达,而在健康组织中通常不存在,这使其成为一种有前景的CAR候选物。在此,我们总结了过去和正在进行的基于NKG2D的CAR临床试验,并对潜在的陷阱进行评论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f43/9327110/ef44df2ae816/ltab018f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f43/9327110/23b9dbb098f1/ltab018f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f43/9327110/ef44df2ae816/ltab018f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f43/9327110/23b9dbb098f1/ltab018f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f43/9327110/ef44df2ae816/ltab018f0002.jpg

相似文献

[1]
A summary of current NKG2D-based CAR clinical trials.

Immunother Adv. 2021-8-13

[2]
NK Cells Expressing a Chimeric Activating Receptor Eliminate MDSCs and Rescue Impaired CAR-T Cell Activity against Solid Tumors.

Cancer Immunol Res. 2019-1-16

[3]
Bispecific antibody-mediated redirection of NKG2D-CAR natural killer cells facilitates dual targeting and enhances antitumor activity.

J Immunother Cancer. 2021-10

[4]
Chimeric Antigen Receptor T Cells Targeting NKG2D-Ligands Show Robust Efficacy Against Acute Myeloid Leukemia and T-Cell Acute Lymphoblastic Leukemia.

Front Immunol. 2020

[5]
T cells expressing NKG2D chimeric antigen receptors efficiently eliminate glioblastoma and cancer stem cells.

J Immunother Cancer. 2019-7-9

[6]
Manufacturing development and clinical production of NKG2D chimeric antigen receptor-expressing T cells for autologous adoptive cell therapy.

Cytotherapy. 2018-6-29

[7]
GMP-Compliant Manufacturing of NKG2D CAR Memory T Cells Using CliniMACS Prodigy.

Front Immunol. 2019-10-10

[8]
Control of triple-negative breast cancer using ex vivo self-enriched, costimulated NKG2D CAR T cells.

J Hematol Oncol. 2018-7-6

[9]
Arming cytotoxic lymphocytes for cancer immunotherapy by means of the NKG2D/NKG2D-ligand system.

Expert Opin Biol Ther. 2020-12

[10]
Eradication of Hepatocellular Carcinoma by NKG2D-Based CAR-T Cells.

Cancer Immunol Res. 2019-9-4

引用本文的文献

[1]
Designs of NKG2D-based immunotherapeutics for cancer.

Front Immunol. 2025-6-19

[2]
Harnessing NKG2D CAR-T cells with radiotherapy: a novel approach for esophageal squamous cell carcinoma treatment.

Front Immunol. 2025-5-29

[3]
Insights into next-generation immunotherapy designs and tools: molecular mechanisms and therapeutic prospects.

J Hematol Oncol. 2025-6-7

[4]
The role of glycan-lectin interactions in the tumor microenvironment: immunosuppression regulators of colorectal cancer.

Am J Cancer Res. 2025-4-15

[5]
Immunotherapy in Breast Cancer: Beyond Immune Checkpoint Inhibitors.

Int J Mol Sci. 2025-4-21

[6]
NKG2D-CAR-targeted iPSC-derived MSCs efficiently target solid tumors expressing NKG2D ligand.

iScience. 2025-4-2

[7]
NKG2D/CD28 chimeric receptor boosts cytotoxicity and durability of CAR-T cells for solid and hematological tumors.

Exp Hematol Oncol. 2025-4-3

[8]
Enhancing CAR T-Cell Function with Domains of Innate Immunity Sensors.

Int J Mol Sci. 2025-2-5

[9]
Emerging combined CAR-NK cell therapies in cancer treatment: Finding a dancing partner.

Mol Ther. 2025-1-3

[10]
CAR-T cell therapy for the treatment of adult high-grade gliomas.

NPJ Precis Oncol. 2024-12-19

本文引用的文献

[1]
Recent advances and discoveries in the mechanisms and functions of CAR T cells.

Nat Rev Cancer. 2021-3

[2]
CAR-NK cells: A promising cellular immunotherapy for cancer.

EBioMedicine. 2020-9

[3]
Gamma-Delta CAR-T Cells Show CAR-Directed and Independent Activity Against Leukemia.

Front Immunol. 2020

[4]
Multispecific Targeting with Synthetic Ankyrin Repeat Motif Chimeric Antigen Receptors.

Clin Cancer Res. 2019-9-23

[5]
Absence of NKG2D ligands defines leukaemia stem cells and mediates their immune evasion.

Nature. 2019-7-17

[6]
Selecting costimulatory domains for chimeric antigen receptors: functional and clinical considerations.

Clin Transl Immunology. 2019-5-11

[7]
Phase I Trial of Autologous CAR T Cells Targeting NKG2D Ligands in Patients with AML/MDS and Multiple Myeloma.

Cancer Immunol Res. 2018-11-5

[8]
NKG2D Ligands-Critical Targets for Cancer Immune Escape and Therapy.

Front Immunol. 2018-9-11

[9]
Manufacturing development and clinical production of NKG2D chimeric antigen receptor-expressing T cells for autologous adoptive cell therapy.

Cytotherapy. 2018-6-29

[10]
Off-the-Shelf CAR-NK Cells for Cancer Immunotherapy.

Cell Stem Cell. 2018-8-2

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