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鉴定杜氏利什曼原虫婴儿前鞭毛体中一种适合用于地中海内脏利什曼病特异性诊断的免疫显性32千道尔顿膜蛋白。

Identification of an immunodominant 32-kilodalton membrane protein of Leishmania donovani infantum promastigotes suitable for specific diagnosis of Mediterranean visceral leishmaniasis.

作者信息

Tebourski F, el Gaied A, Louzir H, Ben Ismail R, Kammoun R, Dellagi K

机构信息

Laboratory of Hematology and Immunopathology, Faculté de Médecine de Tunis, Tunisia.

出版信息

J Clin Microbiol. 1994 Oct;32(10):2474-80. doi: 10.1128/jcm.32.10.2474-2480.1994.

DOI:10.1128/jcm.32.10.2474-2480.1994
PMID:7814485
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC264086/
Abstract

Sera from 35 patients suffering from Mediterranean visceral leishmaniasis (caused by Leishmania donovani infantum) and 59 patients with various forms of cutaneous leishmaniasis prevalent in the sub-Mediterranean countries (caused by Leishmania major, L. donovani infantum, or Leishmania tropica) were tested by immunoblotting and enzyme-linked immunosorbent assay (ELISA) with both membrane and soluble antigens prepared from L. donovani infantum parasites. Control sera were from healthy children (n = 41), adults with nonleishmanial diseases (n = 40), and patients with Chagas' disease (n = 12). A P32 antigen present in the membrane preparation from L. donovani infantum parasites was recognized by 95% of serum specimens from patients with Mediterranean visceral leishmaniasis but not by serum specimens from patients with cutaneous leishmaniasis or sera from control individuals. An ELISA with electroeluted P32 antigen was found to have a specificity and sensitivity of 94% in the serodiagnosis of Mediterranean visceral leishmaniasis. Healthy children with asymptomatic Leishmania infection were seronegative for the P32 antigen by ELISA. These results suggest that antibodies to P32 antigen develop only in patients with visceral leishmaniasis and that the P32 ELISA may be useful in areas where the disease is endemic for discriminating between patients with this disease and those with other clinical conditions.

摘要

采用从婴儿利什曼原虫制备的膜抗原和可溶性抗原,通过免疫印迹法和酶联免疫吸附测定(ELISA)对35例患地中海内脏利什曼病(由婴儿利什曼原虫引起)的患者以及59例患地中海沿岸国家流行的各种皮肤利什曼病(由硕大利什曼原虫、婴儿利什曼原虫或热带利什曼原虫引起)的患者的血清进行检测。对照血清来自健康儿童(n = 41)、患有非利什曼病的成年人(n = 40)以及恰加斯病患者(n = 12)。婴儿利什曼原虫寄生虫膜制剂中存在的一种P32抗原可被95%的地中海内脏利什曼病患者血清标本识别,但不能被皮肤利什曼病患者血清标本或对照个体血清识别。发现用经电洗脱的P32抗原进行ELISA检测,在地中海内脏利什曼病血清诊断中的特异性和敏感性为94%。ELISA检测显示,无症状利什曼原虫感染的健康儿童对P32抗原呈血清阴性。这些结果表明,仅内脏利什曼病患者会产生针对P32抗原的抗体,且P32 ELISA在该病流行地区对于鉴别该病患者与其他临床病症患者可能有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b4b/264086/66f097386643/jcm00010-0147-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b4b/264086/9deef4c19c6a/jcm00010-0146-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b4b/264086/65fd8198345b/jcm00010-0147-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b4b/264086/66f097386643/jcm00010-0147-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b4b/264086/9deef4c19c6a/jcm00010-0146-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b4b/264086/65fd8198345b/jcm00010-0147-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b4b/264086/66f097386643/jcm00010-0147-b.jpg

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