• 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

抗体CD166对荷口腔鳞状细胞癌小鼠肿瘤治疗的影响及免疫机制

The influence of antibody CD166 on the treatment of tumor and the immunological mechanism in mice bearing oral squamous cell carcinoma.

作者信息

Yu Binbin, Li Rui, Zhu Xueqin, Chi Zhengbing

机构信息

Department of Pediatric Dentistry, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, College of Stomatology, Shanghai Jiao Tong University, Shanghai, China.

National Center for Stomatology, National Clinical Research Center for Oral Diseases, Shanghai Key Laboratory of Stomatology, Shanghai Research Institute of Stomatology, Shanghai, China.

出版信息

Transl Cancer Res. 2023 Apr 28;12(4):784-792. doi: 10.21037/tcr-22-2704. Epub 2023 Apr 6.

DOI:10.21037/tcr-22-2704
PMID:37180656
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10174996/
Abstract

BACKGROUND

This study aimed to investigate the influence of antibody CD166 on the inhibition of tumor and further investigate the influence on immune cells of tumor tissues in mice bearing oral squamous cell carcinoma (OSCC).

METHODS

The xenograft model was established through subcutaneously injection of mouse OSCCs cells. Ten mice were randomly divided into two groups. The treatment group was treated with antibody CD166 and the control group was injected with the same volume normal saline. Hematoxylin and eosin (H&E) was used to confirm the tissue histopathology of xenograft mice model. Flow cytometry was used to detect the proportion of CD3CD8 T cells, CD8PD-1 cells and CD11bGr-1 myeloid-derived suppressor cells (MDSCs) cells in the tumor tissues.

RESULTS

After treatment with antibody CD166, the tumor volume and weight in xenograft mice model were significantly reduced. The result of flow cytometry showed that antibody CD166 showed no obvious influence on the proportion of CD3CD8 and CD8PD-1 T lymphocyte cells in the tumor tissues. In the antibody CD166 treatment group, the proportion of CD11bGr-1 MDSCs cells in tumor tissues was 1.930%±0.5317%, which was significantly lower than that of the control group, 4.940%±0.3252% (P=0.0013).

CONCLUSIONS

Antibody CD166 treatment helped reduce the proportion of CD11bGr-1 MDSCs cells, and produced obvious therapeutic effect on the treatment of mice bearing OSCC.

摘要

背景

本研究旨在探讨抗体CD166对肿瘤抑制的影响,并进一步研究其对口腔鳞状细胞癌(OSCC)荷瘤小鼠肿瘤组织免疫细胞的影响。

方法

通过皮下注射小鼠OSCC细胞建立异种移植模型。将10只小鼠随机分为两组。治疗组用抗体CD166治疗,对照组注射相同体积的生理盐水。苏木精和伊红(H&E)染色用于确认异种移植小鼠模型的组织病理学。流式细胞术用于检测肿瘤组织中CD3CD8 T细胞、CD8PD-1细胞和CD11bGr-1髓源性抑制细胞(MDSCs)的比例。

结果

用抗体CD166治疗后,异种移植小鼠模型中的肿瘤体积和重量显著减小。流式细胞术结果显示,抗体CD166对肿瘤组织中CD3CD8和CD8PD-1 T淋巴细胞细胞的比例无明显影响。在抗体CD166治疗组中,肿瘤组织中CD11bGr-1 MDSCs细胞的比例为1.930%±0.5317%,显著低于对照组的4.940%±0.3252%(P=0.0013)。

结论

抗体CD166治疗有助于降低CD11bGr-1 MDSCs细胞的比例,并对OSCC荷瘤小鼠的治疗产生明显的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08f/10174996/73bc2589ca0d/tcr-12-04-784-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08f/10174996/e6baa6de9a95/tcr-12-04-784-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08f/10174996/3cbb7145ff23/tcr-12-04-784-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08f/10174996/a984d264840a/tcr-12-04-784-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08f/10174996/74edf6d5173a/tcr-12-04-784-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08f/10174996/73bc2589ca0d/tcr-12-04-784-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08f/10174996/e6baa6de9a95/tcr-12-04-784-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08f/10174996/3cbb7145ff23/tcr-12-04-784-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08f/10174996/a984d264840a/tcr-12-04-784-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08f/10174996/74edf6d5173a/tcr-12-04-784-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b08f/10174996/73bc2589ca0d/tcr-12-04-784-f5.jpg

相似文献

1
The influence of antibody CD166 on the treatment of tumor and the immunological mechanism in mice bearing oral squamous cell carcinoma.抗体CD166对荷口腔鳞状细胞癌小鼠肿瘤治疗的影响及免疫机制
Transl Cancer Res. 2023 Apr 28;12(4):784-792. doi: 10.21037/tcr-22-2704. Epub 2023 Apr 6.
2
Decidua-derived granulocyte macrophage colony-stimulating factor induces polymorphonuclear myeloid-derived suppressor cells from circulating CD15+ neutrophils.蜕膜衍生粒细胞巨噬细胞集落刺激因子诱导循环 CD15+中性粒细胞中的多形核髓系来源抑制细胞。
Hum Reprod. 2020 Dec 1;35(12):2677-2691. doi: 10.1093/humrep/deaa217.
3
[Myeloid-derived Gr-1⁺ CD11b⁺ suppressor cells are involved in immunoregulation of experimental autoimmune encephalomyelitis].骨髓来源的Gr-1⁺ CD11b⁺抑制细胞参与实验性自身免疫性脑脊髓炎的免疫调节
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2014 Aug;30(8):789-92, 797.
4
Enhanced expression of PD-L1 in oral squamous cell carcinoma-derived CD11b(+)Gr-1(+) cells and its contribution to immunosuppressive activity.口腔鳞状细胞癌来源的CD11b(+)Gr-1(+)细胞中PD-L1的表达增强及其对免疫抑制活性的作用
Oral Oncol. 2016 Aug;59:20-29. doi: 10.1016/j.oraloncology.2016.05.012.
5
Jianpi Huayu Decoction Attenuates the Immunosuppressive Status of H Hepatocellular Carcinoma-Bearing Mice: By Targeting Myeloid-Derived Suppressor Cells.健脾化瘀汤通过靶向髓源性抑制细胞减轻肝癌荷瘤小鼠的免疫抑制状态
Front Pharmacol. 2020 Feb 18;11:16. doi: 10.3389/fphar.2020.00016. eCollection 2020.
6
Polysaccharide Agaricus blazei Murill stimulates myeloid derived suppressor cell differentiation from M2 to M1 type, which mediates inhibition of tumour immune-evasion via the Toll-like receptor 2 pathway.姬松茸多糖刺激髓源性抑制细胞从M2型向M1型分化,其通过Toll样受体2途径介导对肿瘤免疫逃逸的抑制。
Immunology. 2015 Nov;146(3):379-91. doi: 10.1111/imm.12508. Epub 2015 Sep 3.
7
B7-H1 on myeloid-derived suppressor cells in immune suppression by a mouse model of ovarian cancer.通过卵巢癌小鼠模型研究髓源性抑制细胞上的B7-H1在免疫抑制中的作用
Clin Immunol. 2008 Dec;129(3):471-81. doi: 10.1016/j.clim.2008.07.030. Epub 2008 Sep 14.
8
The Combination of MEK Inhibitor With Immunomodulatory Antibodies Targeting Programmed Death 1 and Programmed Death Ligand 1 Results in Prolonged Survival in Kras/p53-Driven Lung Cancer.MEK 抑制剂联合靶向程序性死亡受体 1 和程序性死亡配体 1 的免疫调节抗体可延长 Kras/p53 驱动的肺癌患者的生存时间。
J Thorac Oncol. 2019 Jun;14(6):1046-1060. doi: 10.1016/j.jtho.2019.02.004. Epub 2019 Feb 13.
9
Differences of tumor-recruiting myeloid cells in murine squamous cell carcinoma influence the efficacy of immunotherapy combined with a TLR7 agonist and PD-L1 blockade.在小鼠鳞状细胞癌中,招募肿瘤的髓样细胞的差异影响 TLR7 激动剂和 PD-L1 阻断联合免疫治疗的疗效。
Oral Oncol. 2019 Apr;91:21-28. doi: 10.1016/j.oraloncology.2019.02.014. Epub 2019 Feb 20.
10
Regorafenib enhances antitumor immune efficacy of anti-PD-L1 immunotherapy on oral squamous cell carcinoma.雷戈非尼增强抗 PD-L1 免疫疗法治疗口腔鳞状细胞癌的抗肿瘤免疫疗效。
Biomed Pharmacother. 2022 Mar;147:112661. doi: 10.1016/j.biopha.2022.112661. Epub 2022 Jan 26.

本文引用的文献

1
Targeting myeloid derived suppressor cells reverts immune suppression and sensitizes BRAF-mutant papillary thyroid cancer to MAPK inhibitors.靶向髓系来源抑制细胞可逆转免疫抑制,并使 BRAF 突变型甲状腺乳头状癌对 MAPK 抑制剂敏感。
Nat Commun. 2022 Mar 24;13(1):1588. doi: 10.1038/s41467-022-29000-5.
2
Androgen receptor activity in T cells limits checkpoint blockade efficacy.T 细胞中的雄激素受体活性限制了检查点阻断疗法的疗效。
Nature. 2022 Jun;606(7915):791-796. doi: 10.1038/s41586-022-04522-6. Epub 2022 Mar 23.
3
Metabolic reprograming of MDSCs within tumor microenvironment and targeting for cancer immunotherapy.
肿瘤微环境中 MDSCs 的代谢重编程及其在癌症免疫治疗中的靶向作用。
Acta Pharmacol Sin. 2022 Jun;43(6):1337-1348. doi: 10.1038/s41401-021-00776-4. Epub 2021 Sep 24.
4
MDSC: Markers, development, states, and unaddressed complexity.骨髓来源抑制细胞:标志物、分化、状态和未解决的复杂性。
Immunity. 2021 May 11;54(5):875-884. doi: 10.1016/j.immuni.2021.04.004.
5
Immune suppressive activity of myeloid-derived suppressor cells in cancer requires inactivation of the type I interferon pathway.髓源抑制性细胞在癌症中的免疫抑制活性需要使 I 型干扰素途径失活。
Nat Commun. 2021 Mar 19;12(1):1717. doi: 10.1038/s41467-021-22033-2.
6
Immunotherapy Targeting Myeloid-Derived Suppressor Cells (MDSCs) in Tumor Microenvironment.靶向肿瘤微环境中髓源抑制细胞(MDSCs)的免疫疗法
Front Immunol. 2021 Feb 4;11:585214. doi: 10.3389/fimmu.2020.585214. eCollection 2020.
7
Cancer Statistics, 2021.癌症统计数据,2021.
CA Cancer J Clin. 2021 Jan;71(1):7-33. doi: 10.3322/caac.21654. Epub 2021 Jan 12.
8
CD166 promotes cancer stem cell-like phenotype via the EGFR/ERK1/2 pathway in the nasopharyngeal carcinoma cell line CNE-2R.CD166 通过 EGFR/ERK1/2 通路促进鼻咽癌细胞系 CNE-2R 中的癌症干细胞样表型。
Life Sci. 2021 Feb 15;267:118983. doi: 10.1016/j.lfs.2020.118983. Epub 2020 Dec 29.
9
Tumor Mutational Burden as a Predictor of Immunotherapy Response: Is More Always Better?肿瘤突变负荷作为免疫治疗反应的预测因子:更多是否总是更好?
Clin Cancer Res. 2021 Mar 1;27(5):1236-1241. doi: 10.1158/1078-0432.CCR-20-3054. Epub 2020 Nov 16.
10
The New Era of Cancer Immunotherapy: Targeting Myeloid-Derived Suppressor Cells to Overcome Immune Evasion.癌症免疫治疗的新时代:靶向髓系来源抑制细胞以克服免疫逃逸。
Front Immunol. 2020 Jul 30;11:1680. doi: 10.3389/fimmu.2020.01680. eCollection 2020.