Livni N, Abramowitz A, Londner M, Okon E, Morag A
Virchows Arch A Pathol Anat Histopathol. 1983;401(2):147-51. doi: 10.1007/BF00692639.
An indirect immunoperoxidase technique was applied for identification of Leishmania in routinely prepared histological sections. Paraffin embedded, formalin-fixed slide preparations of skin (1 case), bone marrow (2 cases) and lymph node (1 case) were examined. The tissues were obtained from one patient with cutaneous leishmaniasis and from three patients with visceral leishmaniasis. Specific rabbit antisera against L. donovani, L. tropica and L. mexicana were used as primary reagents. Positive controls were performed simultaneously and included L. tropica cultures in blood-agar (NNN media) - free promastigotes and amastigotes within macrophages. Strongly positive brown staining was localized specifically in Leishman-Donovan (LD) bodies only. This method increases the probability of microscopic diagnosis of leishmaniasis and helps to prevent confusion of Leishmania with other infective agents in histological sections.
采用间接免疫过氧化物酶技术在常规制备的组织学切片中鉴定利什曼原虫。对石蜡包埋、福尔马林固定的皮肤(1例)、骨髓(2例)和淋巴结(1例)玻片标本进行检查。组织取自1例皮肤利什曼病患者和3例内脏利什曼病患者。使用针对杜氏利什曼原虫、热带利什曼原虫和墨西哥利什曼原虫的特异性兔抗血清作为一抗试剂。同时进行阳性对照,包括血琼脂(NNN培养基)中热带利什曼原虫培养物——游离前鞭毛体和巨噬细胞内的无鞭毛体。强阳性棕色染色仅特异性定位于利杜体。该方法提高了利什曼病显微镜诊断的概率,并有助于防止在组织学切片中将利什曼原虫与其他感染因子混淆。