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新型共刺激分子介导的免疫调节

Immune regulation by novel costimulatory molecules.

作者信息

Dong Chen, Nurieva Roza I, Prasad Durbaka V R

机构信息

Department of Immunology, University of Washington School of Medicine, Seattle, WA 98195-7650, USA.

出版信息

Immunol Res. 2003;28(1):39-48. doi: 10.1385/IR:28:1:39.

DOI:10.1385/IR:28:1:39
PMID:12947223
Abstract

CD4 helper T (Th)-cells and the cytokines that they produce play essential regulatory roles in immune and autoimmune responses. Th activation and differentiation is regulated by costimulatory receptors. CD28 and CTLA-4 are important in maintaining the threshold of T-cell activation. ICOS and PD-1 are novel costimulatory receptors expressed on activated T-cells. B7-H3 recognizes a putative costimulatory receptor on activated T-cells. Here we summarize the latest developments in the novel costimulatory molecules and their roles in regulating Th activation, differentiation, and function.

摘要

CD4辅助性T(Th)细胞及其产生的细胞因子在免疫和自身免疫反应中发挥着重要的调节作用。Th细胞的激活和分化受共刺激受体调控。CD28和CTLA-4在维持T细胞激活阈值方面很重要。ICOS和PD-1是在活化T细胞上表达的新型共刺激受体。B7-H3识别活化T细胞上一种假定的共刺激受体。在此,我们总结新型共刺激分子的最新进展及其在调节Th细胞激活、分化和功能方面的作用。

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Immune regulation by novel costimulatory molecules.新型共刺激分子介导的免疫调节
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2
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Nat Immunol. 2001 Mar;2(3):203-9. doi: 10.1038/85251.
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本文引用的文献

1
Characterization of mouse and human B7-H3 genes.小鼠和人类B7-H3基因的特征分析。
J Immunol. 2002 Jun 15;168(12):6294-7. doi: 10.4049/jimmunol.168.12.6294.
2
B7H costimulates clonal expansion of, and cognate destruction of tumor cells by, CD8(+) T lymphocytes in vivo.B7H在体内共刺激CD8(+) T淋巴细胞对肿瘤细胞进行克隆扩增并对其进行同源性杀伤。
J Exp Med. 2001 Nov 5;194(9):1339-48. doi: 10.1084/jem.194.9.1339.
3
The costimulatory molecule ICOS plays an important role in the immunopathogenesis of EAE.共刺激分子ICOS在实验性自身免疫性脑脊髓炎的免疫发病机制中起重要作用。
ICOS 信号促进 Foxp3 转录,有利于调节性 T 细胞的抑制功能。
Int J Med Sci. 2018 Apr 3;15(7):666-673. doi: 10.7150/ijms.23940. eCollection 2018.
4
Unique Features of Pancreatic-Resident Regulatory T Cells in Autoimmune Type 1 Diabetes.自身免疫性1型糖尿病中胰腺驻留调节性T细胞的独特特征
Front Immunol. 2017 Sep 29;8:1235. doi: 10.3389/fimmu.2017.01235. eCollection 2017.
5
Potential targeting of B7-H4 for the treatment of cancer.B7-H4在癌症治疗中的潜在靶向作用。
Immunol Rev. 2017 Mar;276(1):40-51. doi: 10.1111/imr.12530.
6
The co-stimulatory molecule B7-H3 promotes the epithelial-mesenchymal transition in colorectal cancer.共刺激分子B7-H3促进结直肠癌中的上皮-间质转化。
Oncotarget. 2016 May 31;7(22):31755-71. doi: 10.18632/oncotarget.9035.
7
Inducible T-cell co-stimulator ligand (ICOSL) blockade leads to selective inhibition of anti-KLH IgG responses in subjects with systemic lupus erythematosus.诱导型 T 细胞共刺激分子配体 (ICOSL) 阻断导致系统性红斑狼疮患者抗 KLH IgG 反应的选择性抑制。
Lupus Sci Med. 2016 Apr 8;3(1):e000146. doi: 10.1136/lupus-2016-000146. eCollection 2016.
8
Mechanisms of Cholera Toxin in the Modulation of TH17 Responses.霍乱毒素调节TH17反应的机制
Crit Rev Immunol. 2015;35(2):135-52. doi: 10.1615/critrevimmunol.2015012295.
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J Clin Lab Anal. 2015 Sep;29(5):412-8. doi: 10.1002/jcla.21788. Epub 2014 Nov 10.
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Characterization of programmed death-1 homologue-1 (PD-1H) expression and function in normal and HIV infected individuals.程序性死亡-1同源物-1(PD-1H)在正常个体和HIV感染个体中的表达及功能特征
PLoS One. 2014 Oct 3;9(10):e109103. doi: 10.1371/journal.pone.0109103. eCollection 2014.
Nat Immunol. 2001 Jul;2(7):605-11. doi: 10.1038/89750.
4
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J Immunol. 2001 Jul 1;167(1):132-9. doi: 10.4049/jimmunol.167.1.132.
5
ICOS is essential for effective T-helper-cell responses.诱导性共刺激分子(ICOS)对于有效的辅助性T细胞反应至关重要。
Nature. 2001 Jan 4;409(6816):105-9. doi: 10.1038/35051113.
6
ICOS is critical for CD40-mediated antibody class switching.诱导共刺激分子(ICOS)对于CD40介导的抗体类别转换至关重要。
Nature. 2001 Jan 4;409(6816):102-5. doi: 10.1038/35051107.
7
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Nature. 2001 Jan 4;409(6816):97-101. doi: 10.1038/35051100.
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J Immunol. 2001 Mar 15;166(6):3659-62. doi: 10.4049/jimmunol.166.6.3659.
9
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Nat Immunol. 2001 Mar;2(3):269-74. doi: 10.1038/85339.
10
Cell fate decision: T-helper 1 and 2 subsets in immune responses.细胞命运决定:免疫反应中的辅助性T细胞1和2亚群
Arthritis Res. 2000;2(3):179-188. doi: 10.1186/ar85. Epub 2000 Mar 27.