• 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

B7-CD28超家族

The B7-CD28 superfamily.

作者信息

Sharpe Arlene H, Freeman Gordon J

机构信息

Immunology Research Division, Department of Pathology, Brigham, and Women's Hospital, Harvard Medical School, 221 Longwood Avenue, Boston, Massachusetts 02115, USA.

出版信息

Nat Rev Immunol. 2002 Feb;2(2):116-26. doi: 10.1038/nri727.

DOI:10.1038/nri727
PMID:11910893
Abstract

The B7-1/B7-2-CD28/CTLA-4 pathway is crucial in regulating T-cell activation and tolerance. New B7 and CD28 molecules have recently been discovered and new pathways have been delineated that seem to be important for regulating the responses of previously activated T cells. Several B7 homologues are expressed on cells other than professional antigen-presenting cells, indicating new mechanisms for regulating T-cell responses in peripheral tissues. Some B7 homologues have unknown receptors, indicating that other immunoregulatory pathways remain to be described. Here, we summarize our current understanding of the new members of the B7 and CD28 families, and discuss their therapeutic potential.

摘要

B7-1/B7-2-CD28/CTLA-4通路在调节T细胞活化和耐受性方面至关重要。最近发现了新的B7和CD28分子,并描绘了新的通路,这些通路似乎对调节先前活化的T细胞反应很重要。几种B7同源物在专职抗原呈递细胞以外的细胞上表达,这表明在外周组织中调节T细胞反应有新机制。一些B7同源物具有未知受体,这表明其他免疫调节通路有待描述。在这里,我们总结了目前对B7和CD28家族新成员的理解,并讨论了它们的治疗潜力。

相似文献

1
The B7-CD28 superfamily.B7-CD28超家族
Nat Rev Immunol. 2002 Feb;2(2):116-26. doi: 10.1038/nri727.
2
The B7 family of ligands and its receptors: new pathways for costimulation and inhibition of immune responses.B7 配体家族及其受体:共刺激和免疫反应抑制的新途径。
Annu Rev Immunol. 2002;20:29-53. doi: 10.1146/annurev.immunol.20.091101.091806. Epub 2001 Oct 4.
3
The B7 family revisited.重新审视B7家族。
Annu Rev Immunol. 2005;23:515-48. doi: 10.1146/annurev.immunol.23.021704.115611.
4
Co-signaling molecules of the B7-CD28 family in positive and negative regulation of T lymphocyte responses.B7-CD28家族共信号分子在T淋巴细胞反应的正性和负性调节中作用
Microbes Infect. 2004 Jul;6(8):759-66. doi: 10.1016/j.micinf.2004.03.007.
5
CD28 engagement by B7/BB-1 induces transient down-regulation of CD28 synthesis and prolonged unresponsiveness to CD28 signaling.B7/BB-1与CD28结合会诱导CD28合成的短暂下调以及对CD28信号的长期无反应性。
J Immunol. 1993 Apr 15;150(8 Pt 1):3161-9.
6
Activation of human peripheral blood dendritic cells induces the CD86 co-stimulatory molecule.人类外周血树突状细胞的激活可诱导共刺激分子CD86的产生。
Eur J Immunol. 1995 Jul;25(7):2064-8. doi: 10.1002/eji.1830250739.
7
Nucleic acid vaccine-induced immune responses require CD28 costimulation and are regulated by CTLA4.核酸疫苗诱导的免疫反应需要CD28共刺激,并受CTLA4调节。
J Immunol. 1998 Mar 15;160(6):2706-14.
8
T cells of staphylococcal enterotoxin B-tolerized autoimmune MRL-lpr/lpr mice require co-stimulation through the B7-CD28/CTLA-4 pathway for activation and can be reanergized in vivo by stimulation of the T cell receptor in the absence of this co-stimulatory signal.对葡萄球菌肠毒素B耐受的自身免疫性MRL-lpr/lpr小鼠的T细胞需要通过B7-CD28/CTLA-4途径进行共刺激才能激活,并且在缺乏这种共刺激信号的情况下,通过刺激T细胞受体可在体内再次失能。
Eur J Immunol. 1994 May;24(5):1019-25. doi: 10.1002/eji.1830240502.
9
Complexities of CD28/B7: CTLA-4 costimulatory pathways in autoimmunity and transplantation.CD28/B7:CTLA-4共刺激通路在自身免疫和移植中的复杂性
Annu Rev Immunol. 2001;19:225-52. doi: 10.1146/annurev.immunol.19.1.225.
10
ICOS and CD28 reversely regulate IL-10 on re-activation of human effector T cells with mature dendritic cells.ICOS和CD28在成熟树突状细胞重新激活人效应T细胞时对白细胞介素-10进行反向调节。
Eur J Immunol. 2002 Sep;32(9):2680-6. doi: 10.1002/1521-4141(200209)32:9<2680::AID-IMMU2680>3.0.CO;2-6.

引用本文的文献

1
CD4/CD8-p56 Induced T-Cell Receptor Signaling and Its Implications for Immunotherapy.CD4/CD8-p56诱导的T细胞受体信号传导及其对免疫治疗的意义。
Biomolecules. 2025 Jul 29;15(8):1096. doi: 10.3390/biom15081096.
2
First-in-human phase 1 study of the ICOS agonist feladilimab on patients with advanced solid tumors.ICOS激动剂费拉地利单抗用于晚期实体瘤患者的首次人体1期研究。
J Immunother Cancer. 2025 Aug 11;13(8):e011475. doi: 10.1136/jitc-2025-011475.
3
THE BIOLOGY BEHIND PD-1 CHECKPOINT BLOCKADE.PD-1 检查点阻断背后的生物学原理。
Trans Am Clin Climatol Assoc. 2025;135:169-183.
4
Molecular Dynamics of Trogocytosis and Other Contact-Dependent Cell Trafficking Mechanisms in Tumor Pathogenesis.肿瘤发病机制中噬细胞作用及其他接触依赖性细胞转运机制的分子动力学
Cancers (Basel). 2025 Jul 8;17(14):2268. doi: 10.3390/cancers17142268.
5
Functional and structural analysis of missense variants in the human Gene.人类基因中错义变异的功能和结构分析
J Public Health Afr. 2025 Jun 20;16(4):1348. doi: 10.4102/jphia.v16i4.1348. eCollection 2025.
6
Single-cell transcriptomic landscape indicates the potential role of immunotherapy in metastatic pancreatic angiosarcoma.单细胞转录组图谱揭示免疫疗法在转移性胰腺血管肉瘤中的潜在作用。
Gastroenterol Rep (Oxf). 2025 Jun 16;13:goaf046. doi: 10.1093/gastro/goaf046. eCollection 2025.
7
CD28 and ICOS in immune regulation: Structural insights and therapeutic targeting.CD28和ICOS在免疫调节中的作用:结构见解与治疗靶点
Bioorg Med Chem Lett. 2025 Jun 15;127:130310. doi: 10.1016/j.bmcl.2025.130310.
8
Current Treatment of Uveal Melanoma.葡萄膜黑色素瘤的当前治疗方法
Cancers (Basel). 2025 Apr 23;17(9):1403. doi: 10.3390/cancers17091403.
9
Computational Design of a Bicyclic Peptide Inhibitor Targeting the ICOS/ICOS-L Protein-Protein Interaction.靶向ICOS/ICOS-L蛋白-蛋白相互作用的双环肽抑制剂的计算设计
Chem Biol Drug Des. 2025 May;105(5):e70117. doi: 10.1111/cbdd.70117.
10
Single-cell transcriptomic analysis reveals gut microbiota-immunotherapy synergy through modulating tumor microenvironment.单细胞转录组分析揭示肠道微生物群与免疫疗法通过调节肿瘤微环境产生协同作用。
Signal Transduct Target Ther. 2025 May 2;10(1):140. doi: 10.1038/s41392-025-02226-7.