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基于前鞭毛体和无鞭毛体抗原的直接凝集试验在黑热病后皮肤利什曼病血清诊断中的潜力。

Potential of direct agglutination test based on promastigote and amastigote antigens for serodiagnosis of post-kala-azar dermal leishmaniasis.

作者信息

Singh Ruchi, Subba Raju B V, Jain R K, Salotra Poonam

机构信息

Institute of Pathology (ICMR), New Delhi 110029, India.

出版信息

Clin Diagn Lab Immunol. 2005 Oct;12(10):1191-4. doi: 10.1128/CDLI.12.10.1191-1194.2005.

Abstract

Post-kala-azar dermal leishmaniasis (PKDL) is a dermal complication, a sequel to kala-azar. Diagnosis of PKDL presents a challenge due to the low parasite burden in the lesions. The direct agglutination test (DAT) based on promastigote and amastigote antigens of Leishmania donovani of indigenous isolates was developed to diagnose PKDL, and the results were compared with those of the rk39 strip test. The sensitivities of DAT for antileishmanial antibody detection, based on promastigote and amastigote antigens at a cutoff titer of 1:800 were 98.5% and 100%, respectively, with corresponding specificities of 96.5% and 100%. DAT could correctly detect 100% polymorphic cases and 95.4% macular PKDL cases. In comparison, the rk39 strip test was able to correctly diagnose 95.6% of polymorphic and 86.0% macular PKDL cases. DAT based on axenic amastigote antigen provided 100% sensitivity and specificity, making it particularly useful for macular PKDL cases, which are often missed by the rk39 strip test. Thus, DAT provides a simple, reliable, and inexpensive test for PKDL diagnosis with potential applicability in field conditions.

摘要

黑热病后皮肤利什曼病(PKDL)是一种皮肤并发症,是黑热病的后遗症。由于病变中寄生虫负荷较低,PKDL的诊断面临挑战。基于本地分离株杜氏利什曼原虫前鞭毛体和无鞭毛体抗原开发了直接凝集试验(DAT)来诊断PKDL,并将结果与rk39试纸条试验的结果进行比较。在截断效价为1:800时,基于前鞭毛体和无鞭毛体抗原的DAT检测抗利什曼原虫抗体的敏感性分别为98.5%和100%,相应的特异性为96.5%和100%。DAT能够正确检测100%的多形性病例和95.4%的斑疹型PKDL病例。相比之下,rk39试纸条试验能够正确诊断95.6%的多形性病例和86.0%的斑疹型PKDL病例。基于无菌无鞭毛体抗原的DAT提供了100%的敏感性和特异性,使其对斑疹型PKDL病例特别有用,而rk39试纸条试验常常会漏诊这些病例。因此,DAT为PKDL诊断提供了一种简单、可靠且廉价的检测方法,在现场条件下具有潜在的适用性。

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