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自然杀伤 T 细胞在胶质母细胞瘤中的作用。

The Role of NKT Cells in Glioblastoma.

机构信息

Neuro-Oncology Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD 20892, USA.

Nuffield Department of Medicine, Ludwig Institute for Cancer Research, University of Oxford, Oxford OX3 7DQ, UK.

出版信息

Cells. 2021 Jun 30;10(7):1641. doi: 10.3390/cells10071641.


DOI:10.3390/cells10071641
PMID:34208864
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8307781/
Abstract

Glioblastoma is an aggressive and deadly cancer, but to date, immunotherapies have failed to make significant strides in improving prognoses for glioblastoma patients. One of the current challenges to developing immunological interventions for glioblastoma is our incomplete understanding of the numerous immunoregulatory mechanisms at play in the glioblastoma tumor microenvironment. We propose that Natural Killer T (NKT) cells, which are unconventional T lymphocytes that recognize lipid antigens presented by CD1d molecules, may play a key immunoregulatory role in glioblastoma. For example, evidence suggests that the activation of type I NKT cells can facilitate anti-glioblastoma immune responses. On the other hand, type II NKT cells are known to play an immunosuppressive role in other cancers, as well as to cross-regulate type I NKT cell activity, although their specific role in glioblastoma remains largely unclear. This review provides a summary of our current understanding of NKT cells in the immunoregulation of glioblastoma as well as highlights the involvement of NKT cells in other cancers and central nervous system diseases.

摘要

胶质母细胞瘤是一种侵袭性和致命性的癌症,但迄今为止,免疫疗法在改善胶质母细胞瘤患者的预后方面并未取得重大进展。开发胶质母细胞瘤免疫疗法的当前挑战之一是我们对胶质母细胞瘤肿瘤微环境中发挥作用的众多免疫调节机制了解不足。我们提出,自然杀伤 T(NKT)细胞是识别由 CD1d 分子呈递的脂质抗原的非常规 T 淋巴细胞,可能在胶质母细胞瘤中发挥关键的免疫调节作用。例如,有证据表明,I 型 NKT 细胞的激活可以促进抗胶质母细胞瘤免疫反应。另一方面,II 型 NKT 细胞在其他癌症中已知发挥免疫抑制作用,并且可以交叉调节 I 型 NKT 细胞的活性,尽管它们在胶质母细胞瘤中的具体作用在很大程度上仍不清楚。本综述总结了我们目前对 NKT 细胞在胶质母细胞瘤免疫调节中的理解,并强调了 NKT 细胞在其他癌症和中枢神经系统疾病中的参与。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1e/8307781/f4251846a0ce/cells-10-01641-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1e/8307781/58f6beb00978/cells-10-01641-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1e/8307781/f4756e5cd66b/cells-10-01641-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1e/8307781/f4251846a0ce/cells-10-01641-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1e/8307781/58f6beb00978/cells-10-01641-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1e/8307781/f4756e5cd66b/cells-10-01641-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1e/8307781/f4251846a0ce/cells-10-01641-g003.jpg

相似文献

[1]
The Role of NKT Cells in Glioblastoma.

Cells. 2021-6-30

[2]
Tissue-Specific Roles of NKT Cells in Tumor Immunity.

Front Immunol. 2018-8-15

[3]
Type II NKT Cells: An Elusive Population With Immunoregulatory Properties.

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[4]
Altered Lipid Tumor Environment and Its Potential Effects on NKT Cell Function in Tumor Immunity.

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[5]
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[6]
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[7]
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Cancer Immunol Immunother. 2021-5

[8]
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Curr Mol Med. 2009-8

[9]
The immunoregulatory role of type I and type II NKT cells in cancer and other diseases.

Cancer Immunol Immunother. 2014-1-3

[10]
Natural killer T cell activation increases iNOSCD206 M1 macrophage and controls the growth of solid tumor.

J Immunother Cancer. 2019-8-6

引用本文的文献

[1]
Clinical significance of immune cell and biomarker changes in liver cancer.

World J Gastrointest Surg. 2025-6-27

[2]
Comparative evaluation of CAR-expressing T-, NK-, NKT-cells, and macrophages in an immunocompetent mouse glioma model.

Neurooncol Adv. 2025-4-12

[3]
Expanding horizons of cancer immunotherapy: hopes and hurdles.

Front Oncol. 2025-4-25

[4]
CAR-NK cell therapy combined with checkpoint inhibition induces an NKT cell response in glioblastoma.

Br J Cancer. 2025-5

[5]
Balancing Tumor Immunotherapy and Immune-Related Adverse Events: Unveiling the Key Regulators.

Int J Mol Sci. 2024-10-10

[6]
Non-Tumor Cells within the Tumor Microenvironment-The "Eminence Grise" of the Glioblastoma Pathogenesis and Potential Targets for Therapy.

Cells. 2024-5-9

[7]
The tumor micro-environment in pediatric glioma: friend or foe?

Front Immunol. 2023

[8]
Development and validation a prognostic model based on natural killer T cells marker genes for predicting prognosis and characterizing immune status in glioblastoma through integrated analysis of single-cell and bulk RNA sequencing.

Funct Integr Genomics. 2023-8-31

[9]
SFRP4IGFBP5 NKT cells induced neural-like cell differentiation to contribute to adenomyosis pain.

Front Immunol. 2022

[10]
Cellular immunotherapy for medulloblastoma.

Neuro Oncol. 2023-4-6

本文引用的文献

[1]
Making a Cold Tumor Hot: The Role of Vaccines in the Treatment of Glioblastoma.

Front Oncol. 2021-5-10

[2]
Regulation of tumor immune suppression and cancer cell survival by CXCL1/2 elevation in glioblastoma multiforme.

Sci Adv. 2021-1-27

[3]
Functional characterization of the dural sinuses as a neuroimmune interface.

Cell. 2021-2-18

[4]
Innate immunity at the crossroads of healthy brain maturation and neurodevelopmental disorders.

Nat Rev Immunol. 2021-7

[5]
Glioblastoma Immune Landscape and the Potential of New Immunotherapies.

Front Immunol. 2020

[6]
CD1d expression in glioblastoma is a promising target for NKT cell-based cancer immunotherapy.

Cancer Immunol Immunother. 2021-5

[7]
Neutrophil-induced ferroptosis promotes tumor necrosis in glioblastoma progression.

Nat Commun. 2020-10-27

[8]
Zika virus-based immunotherapy enhances long-term survival of rodents with brain tumors through upregulation of memory T-cells.

PLoS One. 2020-10-1

[9]
High Dimensional Single-Cell Analysis Reveals iNKT Cell Developmental Trajectories and Effector Fate Decision.

Cell Rep. 2020-9-8

[10]
Peripherally induced brain tissue-resident memory CD8 T cells mediate protection against CNS infection.

Nat Immunol. 2020-6-22

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