Department of Urology, Lahey Hospital and Medical Center , Burlington , Massachusetts.
Department of Pathology, Lahey Hospital and Medical Center , Burlington , Massachusetts.
J Urol. 2019 Jun;201(6):1158-1163. doi: 10.1097/JU.0000000000000155.
We evaluated the pathophysiology of lichen sclerosus and nonlichen sclerosus urethral stricture disease by comparing protein expression related to inflammation, cell cycle disruption, oxidative stress, hormone receptor status and infection.
Tissue samples were collected from the urethral strictures of 81 patients undergoing urethroplasty. Clinical and demographic data were obtained by chart review. After identifying areas pathognomonic for lichen sclerosus a tissue microarray was created with cores from each sample and immunohistochemistry was performed.
Patients had similar baseline demographics and comorbidities. Of the 81 strictures 58 were and 23 were not due to lichen sclerosus. Lichen sclerosus strictures were significantly longer and showed higher levels of inflammation. The proportion of T cells which stained positive for CD8 was significantly higher in strictures due to lichen sclerosus (50% vs 13%, p = 0.004). CCL-4 was expressed significantly more in strictures due to lichen sclerosus (76% vs 42%, p = 0.01). Several other inflammatory markers were only found in strictures due to lichen sclerosus. Block-like p16, a surrogate for high risk human papillomavirus infection, and varicella zoster virus were found only in lichen sclerosus urethral stricture disease samples, although both were rare. Epstein-Barr virus RNA was found in significantly more lichen sclerosus samples (37% vs 10%, p = 0.024).
To our knowledge this is the first study to evaluate protein expression in lichen sclerosus urethral stricture disease. These strictures demonstrate increased inflammation compared to nonlichen sclerosus urethral strictures. Markers of oxidative stress, cell cycle dysregulation and the androgen receptor do not appear to be uniquely associated with lichen sclerosus urethral stricture disease. Positive staining for several viruses in samples of lichen sclerosus urethral stricture disease suggests a possible infectious etiology.
通过比较与炎症、细胞周期紊乱、氧化应激、激素受体状态和感染相关的蛋白表达,我们评估了硬化性苔藓和非硬化性苔藓尿道狭窄疾病的病理生理学。
收集 81 例行尿道成形术的尿道狭窄患者的尿道狭窄组织标本。通过病历回顾获取临床和人口统计学数据。在确定硬化性苔藓的特征性区域后,使用每个样本的芯创建组织微阵列,并进行免疫组织化学染色。
患者的基线人口统计学和合并症相似。81 处狭窄中有 58 处和 23 处不是由硬化性苔藓引起的。硬化性苔藓性狭窄明显更长,炎症水平更高。硬化性苔藓性狭窄中 CD8 阳性 T 细胞的比例明显更高(50%对 13%,p=0.004)。CCL-4 在硬化性苔藓性狭窄中表达明显更高(76%对 42%,p=0.01)。还有其他一些炎症标志物仅在硬化性苔藓性狭窄中发现。块状 p16,高危型人乳头瘤病毒感染的替代物,和水痘-带状疱疹病毒仅在硬化性苔藓性尿道狭窄疾病样本中发现,尽管这两种病毒都很少见。硬化性苔藓样本中发现 Epstein-Barr 病毒 RNA 的比例明显更高(37%对 10%,p=0.024)。
据我们所知,这是第一项评估硬化性苔藓尿道狭窄疾病中蛋白表达的研究。与非硬化性苔藓性尿道狭窄相比,这些狭窄显示出更高的炎症。氧化应激、细胞周期失调和雄激素受体的标志物似乎与硬化性苔藓性尿道狭窄疾病没有独特的相关性。硬化性苔藓尿道狭窄组织样本中几种病毒的阳性染色提示可能存在感染病因。