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婴儿利什曼原虫抗原抗体的蛋白质印迹分析:14-kD和16-kD抗原用于诊断和流行病学目的的潜力

Western blot analysis of antibodies to Leishmania infantum antigens: potential of the 14-kD and 16-kD antigens for diagnosis and epidemiologic purposes.

作者信息

Mary C, Lamouroux D, Dunan S, Quilici M

机构信息

Laboratoire de Parasitologie, Faculte de Medecine, Marseille, France.

出版信息

Am J Trop Med Hyg. 1992 Dec;47(6):764-71. doi: 10.4269/ajtmh.1992.47.764.

DOI:10.4269/ajtmh.1992.47.764
PMID:1281966
Abstract

When infected with Leishmania species, patients develop specific antibodies that constitute the basis of serodiagnosis. Using Western blot analysis, we studied the specificity of anti-L. infantum antibodies in patients with visceral leishmaniasis (including patients with acquired immunodeficiency syndrome [AIDS]) and in healthy subjects living in an endemic area. Sera from patients with visceral leishmaniasis recognized numerous antigens that had a molecular mass range of 12-120 kD. The 14-, 16-, 28-30-, 46-, and 68-kD antigens were recognized by 92%, 95%, 63%, 80%, 69%, and 89% of the patients' sera, respectively. The 14-16-kD antigens had the greatest specificity for leishmaniasis. The same pattern was found with sera from AIDS patients with proven leishmaniasis, but the 14-kD band was not present in some cases; recognition of the 16-kD band was constant. In these patients, Western blotting characterized specific antibodies even when the results of classic serologic tests (indirect immunofluorescent antibody test and enzyme-linked immunosorbent assay) were negative. Western blotting was found to be more sensitive than the IFA and ELISA, and it was used to detect antibodies to the 14-, 16-, 22-, and 24-kD antigens in subjects living in an endemic area. The detection of antibodies for the 14-kD and 16-kD Leishmania antigens would be a valuable tool both in the diagnosis of visceral leishmaniasis and in epidemiologic studies.

摘要

感染利什曼原虫属物种后,患者会产生特定抗体,这些抗体构成了血清学诊断的基础。我们采用蛋白质印迹分析,研究了内脏利什曼病患者(包括获得性免疫缺陷综合征[艾滋病]患者)及生活在流行地区的健康受试者体内抗婴儿利什曼原虫抗体的特异性。内脏利什曼病患者的血清识别出众多分子量范围在12 - 120 kD的抗原。14 kD、16 kD、28 - 30 kD、46 kD和68 kD的抗原分别被92%、95%、63%、80%、69%和89%的患者血清识别。14 - 16 kD的抗原对利什曼病具有最高的特异性。在确诊为利什曼病的艾滋病患者血清中也发现了相同的模式,但在某些情况下不存在14 kD条带;对16 kD条带的识别是恒定的。在这些患者中,即使经典血清学检测(间接免疫荧光抗体试验和酶联免疫吸附测定)结果为阴性,蛋白质印迹法仍能鉴定出特异性抗体。结果发现蛋白质印迹法比间接免疫荧光法和酶联免疫吸附测定更敏感,并且用于检测生活在流行地区的受试者体内针对14 kD、16 kD、22 kD和24 kD抗原的抗体。检测针对14 kD和16 kD利什曼原虫抗原的抗体,在内脏利什曼病的诊断和流行病学研究中都将是一种有价值的工具。

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