Mengistu G, Kiessling R, Akuffo H
Armauer Hansen Research Institute, Addis Ababa, Ethiopia.
Trans R Soc Trop Med Hyg. 1990 May-Jun;84(3):359-62. doi: 10.1016/0035-9203(90)90317-8.
The usefulness and sensitivity of a direct agglutination test (DAT) in the diagnosis of cutaneous leishmaniasis due to Leishmania aethiopica infection has been investigated. Formalin-fixed, trypsin-treated and Coomassie blue-stained Leishmania promastigotes of various origins were used as antigens. L. major, L. donovani, L. aethiopica but not L. tropica antigen preparations were able to distinguish sera from individuals infected with Leishmania from sera of uninfected controls, although the titres of sera from patients with localized cutaneous leishmaniasis were low. Comparable results were obtained when the same sera were tested using freshly prepared antigen or antigen stored for 10 months at 4 degrees C. The assay was also used to monitor improvement of disease status following treatment of diffuse cutaneous leishmaniasis patients, and it was found to correlate well with the changing clinical status of the patients.
对直接凝集试验(DAT)在诊断由埃塞俄比亚利什曼原虫感染引起的皮肤利什曼病中的实用性和敏感性进行了研究。使用来自不同来源的经福尔马林固定、胰蛋白酶处理并用考马斯亮蓝染色的利什曼原鞭毛虫作为抗原。硕大利什曼原虫、杜氏利什曼原虫、埃塞俄比亚利什曼原虫而非热带利什曼原虫的抗原制剂能够区分感染利什曼原虫个体的血清与未感染对照的血清,尽管局限性皮肤利什曼病患者血清的滴度较低。当使用新鲜制备的抗原或在4℃储存10个月的抗原对相同血清进行检测时,获得了可比的结果。该试验还用于监测弥漫性皮肤利什曼病患者治疗后疾病状态的改善情况,发现其与患者不断变化的临床状态密切相关。