Teirstein A S
Division of Pulmonary and Critical Care Medicine, Mount Sinai Medical Center, and the Mount Sinai School of Medicine, New York, NY 10029, USA.
Semin Respir Infect. 1998 Sep;13(3):206-11.
This article explores the role of the Kveim-Siltzbach (KS) test in finding the cause of sarcoidosis. Experimental granulomas are formed by a T-cell mediated immunologic response to particulate agents which resist degradation and persist in tissues for prolonged periods. There is no animal model for human sarcoidosis. However, the KS test is an in vivo model of sarcoidosis. KS homogenates incite a tissue response in patients with sarcoidosis histologically identical to disease-caused granulomas. The suspensions are particulate and maintain activity when exposed to a variety of chemical and physical stresses. Studies of the monocyte and T-cell host response confirm that KS reagent provokes a sarcoidosis-like antigen driven granuloma. KS suspensions contain an antigen(s) that incite a granuloma identical with that occurring in sarcoidosis. Identification of the active principle in KS suspensions should aid in the search for the cause of sarcoidosis.
本文探讨了克维姆-西尔茨巴赫(KS)试验在寻找结节病病因中的作用。实验性肉芽肿是由T细胞介导的对颗粒性物质的免疫反应形成的,这些颗粒性物质抗降解并在组织中长期存留。人类结节病没有动物模型。然而,KS试验是结节病的一种体内模型。KS匀浆在结节病患者中引发的组织反应在组织学上与疾病所致肉芽肿相同。这些悬液是颗粒性的,在受到各种化学和物理应激时仍保持活性。对单核细胞和T细胞宿主反应的研究证实,KS试剂可引发类似结节病的抗原驱动性肉芽肿。KS悬液含有一种抗原,可引发与结节病中出现的肉芽肿相同的肉芽肿。确定KS悬液中的活性成分应有助于寻找结节病的病因。