Suppr超能文献

自然杀伤细胞是克罗恩病患者体内6-巯基嘌呤的生物学和生化靶点。

NK cells are biologic and biochemical targets of 6-mercaptopurine in Crohn's disease patients.

作者信息

Yusung Susy, McGovern Dermot, Lin Lin, Hommes Daniel, Lagishetty Venu, Braun Jonathan

机构信息

Department of Pediatrics, Harbor UCLA Medical Center and Los Angeles Biomedical Institute, Torrance, CA, United States.

Translational Genomics Group, F. Widjaja Foundation Inflammatory Bowel and Immunobiology Research Institute, and Medical Genetics Institute, Cedars Sinai Medical Center, Los Angeles, CA, United States.

出版信息

Clin Immunol. 2017 Feb;175:82-90. doi: 10.1016/j.clim.2016.12.004. Epub 2016 Dec 21.

Abstract

NK cells, which contribute to immune defense against certain viral infections and neoplasia, are emerging as modifiers of chronic immunologic diseases including transplant rejection and autoimmune diseases. Immunobiology and genetic studies have implicated NK cells as a modifier of Crohn's disease, a condition often treated with thiopurine agents such as 6-mercaptopurine (6-MP). Here, we demonstrate that thiopurines mediate NK cell apoptosis via a caspase 3 and 9 inclusive pathway, and that this process is triggered by thiopurine-mediated inhibition of Rac1. We also show that CD patients in clinical remission maintained on 6-MP have decreased NK cell Rac1 activity, and decreased NK cell numbers in their intestinal biopsies. These observations suggest that thiopurine targeting of NK cells may be a previously unappreciated therapeutic action of these agents in IBD.

摘要

自然杀伤(NK)细胞有助于抵御某些病毒感染和肿瘤形成,在包括移植排斥和自身免疫性疾病在内的慢性免疫疾病中,正逐渐成为调节因子。免疫生物学和遗传学研究表明,NK细胞是克罗恩病的调节因子,这种疾病通常用硫嘌呤类药物如6-巯基嘌呤(6-MP)进行治疗。在此,我们证明硫嘌呤通过包含半胱天冬酶3和9的途径介导NK细胞凋亡,并且这一过程由硫嘌呤介导的Rac1抑制所触发。我们还表明,接受6-MP维持治疗处于临床缓解期的克罗恩病患者,其NK细胞Rac1活性降低,肠道活检中的NK细胞数量减少。这些观察结果表明,硫嘌呤对NK细胞的靶向作用可能是这些药物在炎症性肠病中一种先前未被认识到的治疗作用。

相似文献

1
NK cells are biologic and biochemical targets of 6-mercaptopurine in Crohn's disease patients.
Clin Immunol. 2017 Feb;175:82-90. doi: 10.1016/j.clim.2016.12.004. Epub 2016 Dec 21.
2
Rac1 as a Potential Pharmacodynamic Biomarker for Thiopurine Therapy in Inflammatory Bowel Disease.
Ther Drug Monit. 2016 Oct;38(5):621-7. doi: 10.1097/FTD.0000000000000326.
3
The pharmacokinetic effect of adalimumab on thiopurine metabolism in Crohn's disease patients.
J Crohns Colitis. 2014 Feb;8(2):120-8. doi: 10.1016/j.crohns.2013.07.004. Epub 2013 Aug 7.
4
Rac1 Polymorphisms and Thiopurine Efficacy in Children With Inflammatory Bowel Disease.
J Pediatr Gastroenterol Nutr. 2015 Oct;61(4):404-7. doi: 10.1097/MPG.0000000000000820.
6
Thiopurine effectiveness in patients with Crohn's disease: a study of genetic and clinical predictive factors.
Inflamm Bowel Dis. 2013 Jul;19(8):1639-44. doi: 10.1097/MIB.0b013e31828828d3.
7
Designer Thiopurine-analogues for Optimised Immunosuppression in Inflammatory Bowel Diseases.
J Crohns Colitis. 2016 Oct;10(10):1132-43. doi: 10.1093/ecco-jcc/jjw091. Epub 2016 Apr 25.
8
Thiopurine use associated with reduced B and natural killer cells in inflammatory bowel disease.
World J Gastroenterol. 2017 May 14;23(18):3240-3251. doi: 10.3748/wjg.v23.i18.3240.

引用本文的文献

1
Gut microbiota and intestinal immunity interaction in ulcerative colitis and its application in treatment.
Front Cell Infect Microbiol. 2025 Apr 9;15:1565082. doi: 10.3389/fcimb.2025.1565082. eCollection 2025.
3
WNT2B high‑expressed fibroblasts induce the fibrosis of IBD by promoting NK cells secreting IL-33.
J Mol Med (Berl). 2024 Oct;102(10):1199-1215. doi: 10.1007/s00109-024-02477-x. Epub 2024 Aug 13.
5
Role of Rho GTPases in inflammatory bowel disease.
Cell Death Discov. 2023 Jan 23;9(1):24. doi: 10.1038/s41420-023-01329-w.
6
Effects of metabolic cancer therapy on tumor microenvironment.
Front Oncol. 2022 Dec 13;12:1046630. doi: 10.3389/fonc.2022.1046630. eCollection 2022.
7
Inflammatory Bowel Disease: A Review of Pre-Clinical Murine Models of Human Disease.
Int J Mol Sci. 2022 Aug 19;23(16):9344. doi: 10.3390/ijms23169344.
8
Immune Cell Landscaping Reveals Distinct Immune Signatures of Inflammatory Bowel Disease.
Front Immunol. 2022 Mar 16;13:861790. doi: 10.3389/fimmu.2022.861790. eCollection 2022.
10
Rho GTPases as Key Molecular Players within Intestinal Mucosa and GI Diseases.
Cells. 2021 Jan 4;10(1):66. doi: 10.3390/cells10010066.

本文引用的文献

1
Tissue-Resident NK Cells Mediate Ischemic Kidney Injury and Are Not Depleted by Anti-Asialo-GM1 Antibody.
J Immunol. 2015 Nov 15;195(10):4973-85. doi: 10.4049/jimmunol.1500651. Epub 2015 Oct 9.
2
Innate lymphoid cells. Innate lymphoid cells: a new paradigm in immunology.
Science. 2015 May 22;348(6237):aaa6566. doi: 10.1126/science.aaa6566. Epub 2015 May 21.
3
Control of intestinal homeostasis through crosstalk between natural killer T cells and the intestinal microbiota.
Clin Immunol. 2015 Aug;159(2):128-33. doi: 10.1016/j.clim.2015.05.008. Epub 2015 May 16.
4
6-Mercaptopurine reduces macrophage activation and gut epithelium proliferation through inhibition of GTPase Rac1.
Inflamm Bowel Dis. 2014 Sep;20(9):1487-95. doi: 10.1097/MIB.0000000000000122.
5
Human NK cells licensed by killer Ig receptor genes have an altered cytokine program that modifies CD4+ T cell function.
J Immunol. 2014 Jul 15;193(2):940-9. doi: 10.4049/jimmunol.1400093. Epub 2014 Jun 16.
6
Innate lymphoid cells facilitate NK cell development through a lymphotoxin-mediated stromal microenvironment.
J Exp Med. 2014 Jun 30;211(7):1421-31. doi: 10.1084/jem.20131501. Epub 2014 Jun 9.
7
Functional NK cell repertoires are maintained through IL-2Rα and Fas ligand.
J Immunol. 2014 Apr 15;192(8):3889-97. doi: 10.4049/jimmunol.1302601. Epub 2014 Mar 14.
8
Interleukin 23 in Crohn's disease.
Inflamm Bowel Dis. 2014 Mar;20(3):587-95. doi: 10.1097/01.MIB.0000442014.52661.20.
9
Natural cytotoxicity receptors and their ligands.
Immunol Cell Biol. 2014 Mar;92(3):221-9. doi: 10.1038/icb.2013.98. Epub 2013 Dec 24.
10
IL-2-dependent adaptive control of NK cell homeostasis.
J Exp Med. 2013 Jun 3;210(6):1179-87. doi: 10.1084/jem.20122571. Epub 2013 May 6.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验