Guzman R E, Datta K, Khan N K
Drug Safety Research and Development, Pfizer Global Research and Development, Groton, CT, USA.
Vet Pathol. 2008 Nov;45(6):945-8. doi: 10.1354/vp.45-6-945.
We have observed a renal toxicity consistent with an obstructive protein cast nephropathy in cynomolgus macaques but not in other species treated with different therapeutic candidates having a common carboxylic acid moiety, suggesting a species-specific sensitivity. Here, we present renal toxicity findings consistent with a protein cast nephropathy in a 2-week safety study in cynomolgus monkeys. Light microscopic changes consisted of intratubular cast formation, tubular dilatation, interstitial inflammation, and expansion of the medullary interstitium. Tubular cast material was identified as Tamm-Horsfall protein (THP) and, on ultrastructure, crystalloid material was present in vacuoles of tubular epithelium. It is hypothesized that microcrystal formation in the urinary tubular spaces induces aggregation of THP protein and cast formation in monkeys. Drug-induced obstructive nephropathy is not identified as a major problem in humans; thus, the clinical relevance of the above findings in monkeys is not clear.
我们在食蟹猴中观察到了与梗阻性蛋白管型肾病一致的肾毒性,但在用具有共同羧酸部分的不同治疗候选物处理的其他物种中未观察到,这表明存在物种特异性敏感性。在此,我们展示了在食蟹猴的一项为期2周的安全性研究中与蛋白管型肾病一致的肾毒性发现。光学显微镜下的变化包括肾小管内管型形成、肾小管扩张、间质炎症以及髓质间质扩张。肾小管管型物质被鉴定为Tamm-Horsfall蛋白(THP),并且在超微结构上,晶体物质存在于肾小管上皮细胞的空泡中。据推测,肾小管腔内的微晶形成会诱导食蟹猴体内THP蛋白聚集和管型形成。药物性梗阻性肾病在人类中未被认定为主要问题;因此,上述在食蟹猴中的发现的临床相关性尚不清楚。