Yusung Susy, McGovern Dermot, Lin Lin, Hommes Daniel, Lagishetty Venu, Braun Jonathan
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.
Clin Immunol. 2017 Feb;175:82-90. doi: 10.1016/j.clim.2016.12.004. Epub 2016 Dec 21.
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.
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。