Health Genetics Unit, Institute for Maternal and Child Health-IRCCS Burlo Garofolo, Trieste, Italy.
Pediatr Res. 2013 Sep;74(3):266-71. doi: 10.1038/pr.2013.96. Epub 2013 Jun 12.
Mevalonate kinase deficiency (MKD) is a rare genetic autoinflammatory disease caused by blocking of the enzyme mevalonate kinase in the pathway of cholesterol and isoprenoids. The pathogenic mechanism originating an immune response in MKD patients has not been clearly understood.
We investigated the dysregulation of expression of selected cytokines and chemokines in the serum of MKD patients. The results have been compared with those observed in an MKD mouse model obtained by treating the mice with aminobisphosphonate, a molecule that is able to inhibit the cholesterol pathway, mimicking the genetic block characteristic of the disease.
Interleukin (IL)-1β, IL-5, IL-6, IL-9, IL-17, granulocyte colony-stimulating factor, monocyte chemotactic protein-1, tumor necrosis factor-α, and IL-4 expression were dysregulated in sera from MKD patients and mice. Moreover, geraniol, an exogenous isoprenoid, when administered to MKD mice, restored cytokines and chemokines levels with values similar to those of untreated mice.
Our findings, which were obtained in patients and a mouse model mimicking the human disease, suggest that these cytokines and chemokines could be MKD specific and that isoprenoids could be considered as potential therapeutic molecules. The mouse model, even if with some limitations, was robust and suitable for routine testing of potential MKD drugs.
甲羟戊酸激酶缺乏症(MKD)是一种罕见的遗传性自身炎症性疾病,由胆固醇和异戊烯途径中酶甲羟戊酸激酶的阻断引起。MKD 患者产生免疫反应的发病机制尚未明确。
我们研究了 MKD 患者血清中选定细胞因子和趋化因子表达的失调。将这些结果与通过用能够抑制胆固醇途径的分子氨基双膦酸盐处理小鼠获得的 MKD 小鼠模型中观察到的结果进行了比较,该分子模拟了疾病的遗传阻断特征。
MKD 患者和小鼠的血清中白细胞介素(IL)-1β、IL-5、IL-6、IL-9、IL-17、粒细胞集落刺激因子、单核细胞趋化蛋白-1、肿瘤坏死因子-α和 IL-4 的表达失调。此外,给予 MKD 小鼠香叶醇(一种外源性异戊烯)可恢复细胞因子和趋化因子水平,使其与未治疗的小鼠相似。
我们在患者和模拟人类疾病的小鼠模型中获得的发现表明,这些细胞因子和趋化因子可能是 MKD 特异性的,异戊烯类化合物可以被认为是潜在的治疗分子。即使存在一些限制,该小鼠模型仍然稳健且适合常规测试潜在的 MKD 药物。