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抗天然DNA抗体:通过免疫过氧化物酶测定法进行检测及其免疫球蛋白类别的测定

Antibodies to native DNA: detection by immunoperoxidase assay and determination of their immunoglobulin classes.

作者信息

Vladutiu A O, Palumbo D A, Asirwatham J E

出版信息

Clin Chem. 1979 Mar;25(3):366-70.

PMID:400438
Abstract

Antinuclear antibodies are almost always found in sera of patients with systemic lupus erythematosus. To differentiate antinuclear antibodies from antibodies to DNA in the recently described Crithidia luciliae assay, we developed an immunoperoxidase technique for detecting antibodies to native, double-stranded DNA and compared results by it with those by the Farr assay. Smears of cultured Crithidia luciliae were incubated with human sera, peroxidase-labeled anti-human IgG serum, and diaminobenzidine. The peroxidase stain was examined by conventional light microscopy, which facilitated differentiation between the kinetoplast and the nuclear staining. The Crithidia assay appeared to be specific for double-stranded DNA antibodies, seemed to be more sensitive than the Farr assay, and allowed us to determine the immunoglobulin classes of antibodies to native DNA. Some patients with systemic lupus erythematosus had only IgM or IgA antibodies to DNA.

摘要

抗核抗体几乎总是在系统性红斑狼疮患者的血清中被发现。为了在最近描述的利什曼原虫检测中区分抗核抗体和抗DNA抗体,我们开发了一种免疫过氧化物酶技术来检测抗天然双链DNA抗体,并将其结果与Farr检测法的结果进行比较。将培养的利什曼原虫涂片与人血清、过氧化物酶标记的抗人IgG血清和二氨基联苯胺一起孵育。通过传统光学显微镜检查过氧化物酶染色,这有助于区分动基体和细胞核染色。利什曼原虫检测似乎对双链DNA抗体具有特异性,似乎比Farr检测更敏感,并且使我们能够确定抗天然DNA抗体的免疫球蛋白类别。一些系统性红斑狼疮患者只有抗DNA的IgM或IgA抗体。

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