• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Immunobiology and conflicting roles of the human NKG2D lymphocyte receptor and its ligands in cancer.人类 NKG2D 淋巴细胞受体及其配体在癌症中的免疫生物学和冲突作用。
J Immunol. 2013 Aug 15;191(4):1509-15. doi: 10.4049/jimmunol.1301071.
2
ULBPs, human ligands of the NKG2D receptor, stimulate tumor immunity with enhancement by IL-15.ULBP是NKG2D受体的人类配体,可通过IL-15增强作用刺激肿瘤免疫。
Blood. 2006 Aug 15;108(4):1313-9. doi: 10.1182/blood-2005-11-011320. Epub 2006 Apr 18.
3
Evasion from NK cell immunity by MHC class I chain-related molecules expressing colon adenocarcinoma.表达于结肠腺癌的MHC I类链相关分子对自然杀伤细胞免疫的逃逸
J Immunol. 2003 Dec 15;171(12):6891-9. doi: 10.4049/jimmunol.171.12.6891.
4
Effect of NKG2D ligand expression on host immune responses.NKG2D 配体表达对宿主免疫反应的影响。
Immunol Rev. 2010 May;235(1):267-85. doi: 10.1111/j.0105-2896.2010.00893.x.
5
Immunobiology of human NKG2D and its ligands.人类自然杀伤细胞2D(NKG2D)及其配体的免疫生物学
Curr Top Microbiol Immunol. 2006;298:121-38. doi: 10.1007/3-540-27743-9_6.
6
Generation of soluble NKG2D ligands: proteolytic cleavage, exosome secretion and functional implications.可溶性 NKG2D 配体的产生:蛋白水解切割、外泌体分泌及其功能意义。
Scand J Immunol. 2013 Aug;78(2):120-9. doi: 10.1111/sji.12072.
7
Human tumor-derived exosomes down-modulate NKG2D expression.人肿瘤来源的外泌体下调NKG2D表达。
J Immunol. 2008 Jun 1;180(11):7249-58. doi: 10.4049/jimmunol.180.11.7249.
8
NKG2D Ligands-Critical Targets for Cancer Immune Escape and Therapy.NKG2D 配体——癌症免疫逃逸和治疗的关键靶点。
Front Immunol. 2018 Sep 11;9:2040. doi: 10.3389/fimmu.2018.02040. eCollection 2018.
9
Antitumor immunity. A shed NKG2D ligand that promotes natural killer cell activation and tumor rejection.抗肿瘤免疫。一种脱落的NKG2D配体,可促进自然杀伤细胞活化和肿瘤排斥。
Science. 2015 Apr 3;348(6230):136-9. doi: 10.1126/science.1258867. Epub 2015 Mar 5.
10
Natural killer group 2D receptor and its ligands in cancer immune escape.自然杀伤细胞组 2D 受体及其配体在癌症免疫逃逸中的作用。
Mol Cancer. 2019 Feb 27;18(1):29. doi: 10.1186/s12943-019-0956-8.

引用本文的文献

1
Gamma delta T cells in cancer therapy: from tumor recognition to novel treatments.癌症治疗中的γδ T细胞:从肿瘤识别到新型治疗方法
Front Med (Lausanne). 2024 Dec 19;11:1480191. doi: 10.3389/fmed.2024.1480191. eCollection 2024.
2
MHC class I polypeptide-related sequence B shedding modulates pancreatic tumor immunity via the activation of NKG2D T cells.MHC Ⅰ类多肽相关序列 B 的脱落通过激活 NKG2D T 细胞调节胰腺肿瘤免疫。
Sci Rep. 2024 Oct 8;14(1):23401. doi: 10.1038/s41598-024-73712-1.
3
Human NK cells and cancer.人自然杀伤细胞与癌症。
Oncoimmunology. 2024 Jul 16;13(1):2378520. doi: 10.1080/2162402X.2024.2378520. eCollection 2024.
4
Chimeric Antigen Receptor T Cell Therapy for Pancreatic Cancer: A Review of Current Evidence.嵌合抗原受体 T 细胞疗法治疗胰腺癌:现有证据的综述。
Cells. 2024 Jan 4;13(1):101. doi: 10.3390/cells13010101.
5
Lenalidomide improves NKG2D-based CAR-T cell activity against colorectal cancer cells invitro.来那度胺可提高基于NKG2D的嵌合抗原受体T细胞(CAR-T细胞)在体外对结肠癌细胞的活性。
Heliyon. 2023 Sep 27;9(10):e20460. doi: 10.1016/j.heliyon.2023.e20460. eCollection 2023 Oct.
6
Valproic acid increases CAR T cell cytotoxicity against acute myeloid leukemia.丙戊酸增强 CAR T 细胞对急性髓系白血病的细胞毒性。
J Immunother Cancer. 2023 Jul;11(7). doi: 10.1136/jitc-2023-006857.
7
models to study natural killer cell dynamics in the tumor microenvironment.用于研究肿瘤微环境中自然杀伤细胞动态的模型。
Front Immunol. 2023 Jun 28;14:1135148. doi: 10.3389/fimmu.2023.1135148. eCollection 2023.
8
Combination therapy of DKK1 inhibition and NKG2D chimeric antigen receptor T cells for the treatment of gastric cancer.DKK1 抑制与 NKG2D 嵌合抗原受体 T 细胞联合治疗胃癌。
Cancer Sci. 2023 Jul;114(7):2798-2809. doi: 10.1111/cas.15828. Epub 2023 May 7.
9
The roles of lncRNA functions and regulatory mechanisms in the diagnosis and treatment of hepatocellular carcinoma.长链非编码RNA功能及调控机制在肝细胞癌诊断与治疗中的作用
Front Cell Dev Biol. 2022 Nov 18;10:1051306. doi: 10.3389/fcell.2022.1051306. eCollection 2022.
10
Upregulation of NKG2D ligands impairs hematopoietic stem cell function in Fanconi anemia.NKG2D 配体的上调会损害范可尼贫血症患者造血干细胞的功能。
J Clin Invest. 2022 Aug 1;132(15). doi: 10.1172/JCI142842.

本文引用的文献

1
Novel immune modulators used in hematology: impact on NK cells.新型免疫调节剂在血液学中的应用:对 NK 细胞的影响。
Front Immunol. 2013 Jan 3;3:388. doi: 10.3389/fimmu.2012.00388. eCollection 2012.
2
Regulation of ligands for the NKG2D activating receptor.NKG2D 激活受体配体的调节。
Annu Rev Immunol. 2013;31:413-41. doi: 10.1146/annurev-immunol-032712-095951. Epub 2013 Jan 3.
3
Chimeric NKG2D CAR-expressing T cell-mediated attack of human ovarian cancer is enhanced by histone deacetylase inhibition.组蛋白去乙酰化酶抑制增强嵌合型 NKG2D CAR 表达 T 细胞对人卵巢癌的攻击。
Hum Gene Ther. 2013 Mar;24(3):295-305. doi: 10.1089/hum.2012.143. Epub 2013 Mar 1.
4
Comprehensive analysis of NKG2D ligand expression and release in leukemia: implications for NKG2D-mediated NK cell responses.白血病中 NKG2D 配体表达和释放的综合分析:对 NKG2D 介导的 NK 细胞反应的影响。
J Immunol. 2012 Aug 1;189(3):1360-71. doi: 10.4049/jimmunol.1200796. Epub 2012 Jun 22.
5
Prevalence of the NKG2D Thr72Ala polymorphism in patients with cervical carcinoma.宫颈癌患者中NKG2D苏氨酸72位点至丙氨酸多态性的患病率
Genet Test Mol Biomarkers. 2012 Aug;16(8):841-5. doi: 10.1089/gtmb.2011.0308. Epub 2012 Apr 5.
6
Redirecting T cells to Ewing's sarcoma family of tumors by a chimeric NKG2D receptor expressed by lentiviral transduction or mRNA transfection.通过慢病毒转导或 mRNA 转染表达的嵌合 NKG2D 受体将 T 细胞重定向至尤文氏肉瘤家族肿瘤。
PLoS One. 2012;7(2):e31210. doi: 10.1371/journal.pone.0031210. Epub 2012 Feb 15.
7
Immune surveillance and therapy of lymphomas driven by Epstein-Barr virus protein LMP1 in a mouse model.在小鼠模型中,由 Epstein-Barr 病毒蛋白 LMP1 驱动的淋巴瘤的免疫监视和治疗。
Cell. 2012 Feb 17;148(4):739-51. doi: 10.1016/j.cell.2011.12.031.
8
NKG2D ligand tumor expression and association with clinical outcome in early breast cancer patients: an observational study.NKG2D 配体肿瘤表达与早期乳腺癌患者临床结局的相关性:一项观察性研究。
BMC Cancer. 2012 Jan 18;12:24. doi: 10.1186/1471-2407-12-24.
9
Expression of ERp5 and GRP78 on the membrane of chronic lymphocytic leukemia cells: association with soluble MICA shedding.慢性淋巴细胞白血病细胞膜上的 ERp5 和 GRP78 的表达:与可溶性 MICA 脱落的关联。
Cancer Immunol Immunother. 2012 Aug;61(8):1201-10. doi: 10.1007/s00262-011-1195-z. Epub 2012 Jan 4.
10
CEACAM1 dampens antitumor immunity by down-regulating NKG2D ligand expression on tumor cells.CEACAM1 通过下调肿瘤细胞上的 NKG2D 配体表达来抑制抗肿瘤免疫。
J Exp Med. 2011 Dec 19;208(13):2633-40. doi: 10.1084/jem.20102575. Epub 2011 Dec 5.

人类 NKG2D 淋巴细胞受体及其配体在癌症中的免疫生物学和冲突作用。

Immunobiology and conflicting roles of the human NKG2D lymphocyte receptor and its ligands in cancer.

机构信息

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

出版信息

J Immunol. 2013 Aug 15;191(4):1509-15. doi: 10.4049/jimmunol.1301071.

DOI:10.4049/jimmunol.1301071
PMID:23913973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3736343/
Abstract

Cancers adopt diverse strategies to safeguard their survival, which often involve blinding or incapacitating the immune response, thereby gaining battleground advantage against the host. In immune responses against cancer, an important stimulatory lymphocyte receptor is NKG2D because the tumor-associated expression of its ligands promotes destruction of malignant cells. However, with advanced human cancers profound changes unfold wherein NKG2D and its ligands are targeted or exploited for immune evasion and suppression. This negative imprinting on the immune system may be accompanied by another functional state wherein cancer cells coopt expression of NKG2D to complement the presence of its ligands for self-stimulation of tumor growth and presumably malignant progression. This review emphasizes these conflicting functional dynamics at the immunity-cancer biology interface in humans, within an overview of the immunobiology of NKG2D and mechanisms underlying the regulation of its ligands in cancer, with reference to instructive clinical observations and translational approaches.

摘要

癌症采用多种策略来保护其生存,其中经常涉及蒙蔽或使免疫反应丧失能力,从而在与宿主的对抗中获得战场优势。在针对癌症的免疫反应中,NKG2D 是一种重要的刺激性淋巴细胞受体,因为其配体在肿瘤相关表达促进了恶性细胞的破坏。然而,在晚期人类癌症中,深刻的变化发生了,其中 NKG2D 及其配体成为免疫逃逸和抑制的目标或被利用。这种对免疫系统的负面印记可能伴随着另一种功能状态,其中癌细胞篡夺 NKG2D 的表达以补充其配体的存在,以自我刺激肿瘤生长,并推测恶性进展。在概述 NKG2D 的免疫生物学和癌症中其配体调节的机制的基础上,本综述强调了人类免疫 - 癌症生物学界面上这些相互矛盾的功能动态,并参考了有益的临床观察和转化方法。