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TLR7/8 激动剂触发人 6-硫酸唾液酸 LacNAc 树突状细胞的免疫刺激特性。

TLR7/8 agonists trigger immunostimulatory properties of human 6-sulfo LacNAc dendritic cells.

机构信息

Institute of Immunology, Medical Faculty, Technical University of Dresden, Dresden, Germany.

出版信息

Cancer Lett. 2013 Jul 10;335(1):119-27. doi: 10.1016/j.canlet.2013.02.003. Epub 2013 Feb 9.


DOI:10.1016/j.canlet.2013.02.003
PMID:23402811
Abstract

Imiquimod and resiquimod represent Toll-like receptor (TLR) 7 and 8 agonists, which emerged as attractive candidates for tumor therapy. To elucidate immune cells, which mainly contribute to TLR7/8-mediated antitumoral activity, we investigated the impact of imiquimod and resiquimod on native human 6-sulfo LacNAc (slan) dendritic cells (DCs). We found that both TLR7/8 agonists significantly improve the release of various proinflammatory cytokines by slanDCs and promote their tumor-directed cytotoxic activity. Furthermore, resiquimod efficiently augmented the ability of slanDCs to stimulate T cells and natural killer cells. These results indicate that imiquimod and resiquimod trigger various immunostimulatory properties of slanDCs, which may contribute to their antitumor effects.

摘要

咪喹莫特和瑞喹莫特是 Toll 样受体 (TLR) 7 和 8 的激动剂,它们作为肿瘤治疗的有吸引力的候选药物而出现。为了阐明主要有助于 TLR7/8 介导的抗肿瘤活性的免疫细胞,我们研究了咪喹莫特和瑞喹莫特对天然人 6-硫酸神经氨酸 (sLan) 树突状细胞 (DCs) 的影响。我们发现,两种 TLR7/8 激动剂都显著提高了 slanDCs 释放各种促炎细胞因子的能力,并促进了它们的肿瘤定向细胞毒性活性。此外,瑞喹莫特有效地增强了 slanDCs 刺激 T 细胞和自然杀伤细胞的能力。这些结果表明,咪喹莫特和瑞喹莫特触发了 slanDCs 的各种免疫刺激特性,这可能有助于它们的抗肿瘤作用。

相似文献

[1]
TLR7/8 agonists trigger immunostimulatory properties of human 6-sulfo LacNAc dendritic cells.

Cancer Lett. 2013-2-9

[2]
Cancer immunotherapeutic potential of novel small molecule TLR7 and TLR8 agonists.

J Immunotoxicol. 2009-12

[3]
The TLR7/8 ligand resiquimod targets monocyte-derived dendritic cell differentiation via TLR8 and augments functional dendritic cell generation.

Cell Immunol. 2011-8-22

[4]
Impact of chemotherapeutic agents on the immunostimulatory properties of human 6-sulfo LacNAc+ (slan) dendritic cells.

Int J Cancer. 2012-11-16

[5]
Reciprocal activating interaction between 6-sulfo LacNAc+ dendritic cells and NK cells.

Int J Cancer. 2009-1-15

[6]
Radiotherapy combined with TLR7/8 activation induces strong immune responses against gastrointestinal tumors.

Oncotarget. 2015-3-10

[7]
Plasmacytoid dendritic cells produce cytokines and mature in response to the TLR7 agonists, imiquimod and resiquimod.

Cell Immunol. 2002

[8]
Generation of Th1-polarizing dendritic cells using the TLR7/8 agonist CL075.

J Immunol. 2010-5-28

[9]
Reversal of human papillomavirus-specific T cell immune suppression through TLR agonist treatment of Langerhans cells exposed to human papillomavirus type 16.

J Immunol. 2009-3-1

[10]
TLR7 and TLR8 as targets in cancer therapy.

Oncogene. 2008-1-7

引用本文的文献

[1]
And Yet It Moves: Oxidation of the Nuclear Autoantigen La/SS-B Is the Driving Force for Nucleo-Cytoplasmic Shuttling.

Int J Mol Sci. 2021-9-8

[2]
6-Sulfo LacNAc (Slan) as a Marker for Non-classical Monocytes.

Front Immunol. 2019-9-13

[3]
Current Concepts on 6-sulfo LacNAc Expressing Monocytes (slanMo).

Front Immunol. 2019-5-22

[4]
IL-1β limits the extent of human 6-sulfo LacNAc dendritic cell (slanDC)-mediated NK cell activation and regulates CD95-induced apoptosis.

Cell Mol Immunol. 2016-4-18

[5]
Structure Based Modeling of Small Molecules Binding to the TLR7 by Atomistic Level Simulations.

Molecules. 2015-5-8

[6]
Tumoricidal activity of human dendritic cells.

Trends Immunol. 2013-11-18

[7]
Imiquimod directly inhibits Hedgehog signalling by stimulating adenosine receptor/protein kinase A-mediated GLI phosphorylation.

Oncogene. 2013-9-2

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