Division of Nephrology, Montefiore Medical Center, Bronx, NY 10466, USA.
Am J Kidney Dis. 2011 May;57(5):752-5. doi: 10.1053/j.ajkd.2010.12.010. Epub 2011 Feb 4.
Diffuse infiltrative lymphocytosis syndrome (DILS) is believed to be an immunologic syndrome, most likely in response to human immunodeficiency virus (HIV) antigens, and can be accompanied by decreased kidney function. The spectrum of kidney involvement includes acute or chronic kidney disease, primarily tubular proteinuria; enlarged kidneys on imaging studies; and dense lymphocytic tubulointerstitial infiltrates predominantly composed of CD8(+) T cells on kidney biopsy. We describe 3 newly diagnosed HIV-positive patients of African descent with the histologic and clinical diagnosis of DILS who presented with acute kidney injury associated with Gram-negative bacterial infections. Solely with specific antibiotic therapy without antiviral and/or corticosteroid therapy, all patients recovered from acute kidney injury and had partial to complete resolution of proteinuria and enlarged kidney size. These observations led us to hypothesize that an altered immunologic and/or inflammatory response to the endotoxin derived from Gram-negative bacteria, rather than an immunologic response directed to HIV-related antigens, may be a pathogenetic mechanism for the kidney disease associated with DILS in a subset of HIV-positive patients, especially those of immunogenetically susceptible African descent.
弥漫浸润性淋巴细胞增多症(DILS)被认为是一种免疫综合征,很可能是对人类免疫缺陷病毒(HIV)抗原的反应,并且可能伴有肾功能下降。肾脏受累的范围包括急性或慢性肾脏病,主要是管状蛋白尿;影像学研究显示肾脏增大;肾活检显示致密的淋巴细胞性肾小管间质浸润,主要由 CD8(+)T 细胞组成。我们描述了 3 例新诊断的 HIV 阳性、非洲裔患者,其组织学和临床诊断为 DILS,表现为与革兰氏阴性菌感染相关的急性肾损伤。仅采用特定的抗生素治疗,而不采用抗病毒和/或皮质类固醇治疗,所有患者的急性肾损伤均得到恢复,并且蛋白尿和肾脏增大的情况部分或完全得到缓解。这些观察结果使我们假设,对源自革兰氏阴性菌的内毒素的免疫和/或炎症反应的改变,而不是针对 HIV 相关抗原的免疫反应,可能是与 DILS 相关的肾脏疾病的发病机制,特别是在具有免疫遗传易感性的非洲裔 HIV 阳性患者中。