Islam Mohammad Zahidul, Itoh Makoto, Takagi Hidekazu, Islam Anwar Ul, Ekram A R M Saifuddin, Rahman Ajijur, Takesue Atsuhide, Hashiguchi Yoshihisa, Kimura Eisaku
Department of Parasitology, Aichi Medical University School of Medicine, Nagakute, Aichi, Japan.
Am J Trop Med Hyg. 2008 Oct;79(4):599-604.
We recently reported the production of the recombinant kinesin-related protein of Leishmania donovani with a molecular weight of 42 kd (rKRP42) and the value of the antigen in serum-based ELISA for the diagnosis of visceral leishmaniasis (VL). In this study, the rKRP42 antigen was validated with ELISA using urine samples (rKRP42 urine ELISA). The urine-based ELISA showed 94% sensitivity (108 positives among 115 VL samples) and 99.6% specificity (239 negatives among 240 non-VL samples). The sensitivity and specificity are almost similar to our previous results by ELISA with acetone-treated L. donovani promastigote antigen and direct agglutination test, both methods being done by use of urine samples. A comparison of the rKRP42 urine ELISA with the commercially available urinary antigen detection kit (KAtex) using 108 VL samples showed much higher sensitivity of the ELISA (96.3%) than KAtex (55.6%). The use of the rKRP42 antigen with urine samples will facilitate epidemiologic studies.
我们最近报道了杜氏利什曼原虫重组驱动蛋白相关蛋白(分子量为42kd,即rKRP42)的产生以及该抗原在基于血清的酶联免疫吸附测定(ELISA)中用于内脏利什曼病(VL)诊断的价值。在本研究中,使用尿液样本通过ELISA对rKRP42抗原进行了验证(rKRP42尿液ELISA)。基于尿液的ELISA显示敏感性为94%(115份VL样本中有108份呈阳性),特异性为99.6%(240份非VL样本中有239份呈阴性)。其敏感性和特异性与我们之前使用经丙酮处理的杜氏利什曼原虫前鞭毛体抗原进行ELISA以及直接凝集试验的结果几乎相似,这两种方法均使用尿液样本。使用108份VL样本将rKRP42尿液ELISA与市售尿液抗原检测试剂盒(KAtex)进行比较,结果显示ELISA的敏感性(96.3%)远高于KAtex(55.6%)。rKRP42抗原与尿液样本的使用将有助于流行病学研究。