Kaldany R R, Maasho K, Ohman R, Reitz-Vick D, Britton S, Lefford M J
Scand J Immunol. 1987 Jan;25(1):37-43. doi: 10.1111/j.1365-3083.1987.tb01044.x.
Two methods for detecting the phenolic glycolipid, PGL-1, a Mycobacterium leprae-specific molecule, in the urine of leprosy patients are described. Both methods rely on the 100-fold preconcentration of the urine, which can be accomplished by a single-step ultrafiltration procedure. The equivalent of approximately 2.5 micrograms of PGL-1/ml was detected in the urine of LL patients with an inhibition ELISA. The second method, a direct dot-blot assay on nitrocellulose paper, was much simpler and more sensitive. As little as 3 ng of antigen was detected by the dot-blot technique. PGL-1 was detected in the urine of LL patients.
本文描述了两种检测麻风病人尿液中酚糖脂-1(PGL-1,一种麻风杆菌特异性分子)的方法。两种方法均依赖于尿液100倍的预浓缩,这可通过单步超滤程序实现。用抑制性酶联免疫吸附测定法在LL型麻风病人的尿液中检测到了相当于约2.5微克/毫升的PGL-1。第二种方法是在硝酸纤维素纸上进行直接斑点印迹分析,该方法更为简单且更灵敏。斑点印迹技术能检测到低至3纳克的抗原。在LL型麻风病人的尿液中检测到了PGL-1。