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利用患者血清,通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳免疫过氧化物酶技术(SGIP)对麻风分枝杆菌抗原进行免疫化学特性分析。

Immunochemical characterization of Mycobacterium leprae antigens by the SDS-polyacrylamide gel electrophoresis immunoperoxidase technique (SGIP) using patients' sera.

作者信息

Klatser P R, van Rens M M, Eggelte T A

出版信息

Clin Exp Immunol. 1984 Jun;56(3):537-44.

PMID:6378452
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1536007/
Abstract

In this study the SDS-polyacrylamide gel electrophoresis immunoperoxidase (SGIP) assay was used for characterizing the antigenic components of Mycobacterium leprae using patients' sera. This technique involved the separation of mycobacterial sonicates on SDS-polyacrylamide gels, longitudinal sectioning of the gels, incubation with patients' sera and visualization of the antigen-antibody complexes by the indirect immunoperoxidase technique. A number of antigens present in M. leprae sonicates were recognized by leprosy patients' sera, some of which were seen in other mycobacteria as well. Antibody binding to a 33 kD antigen, present in both M. leprae and BCG sonicates, was reduced only in the latter after 6 months of multiple drug treatment of one patient. It is suggested that this is a common mycobacterial antigen with one or more M. leprae specific determinants. Several antigens were identified only in M. leprae sonicates, only by leprosy patients: a 12, 22, 28, 36, 41 and 86 kD component. These antigens lost their antigenicity after trypsin treatment, but were heat stable. Such M. leprae specific antigens may be useful for immunodiagnosis.

摘要

在本研究中,采用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳免疫过氧化物酶(SGIP)测定法,利用患者血清来鉴定麻风分枝杆菌的抗原成分。该技术包括在十二烷基硫酸钠-聚丙烯酰胺凝胶上分离分枝杆菌超声裂解物,对凝胶进行纵向切片,与患者血清孵育,并通过间接免疫过氧化物酶技术使抗原-抗体复合物可视化。麻风分枝杆菌超声裂解物中的多种抗原可被麻风患者血清识别,其中一些在其他分枝杆菌中也可见。一名患者接受多药治疗6个月后,仅在卡介苗超声裂解物中存在的一种33kD抗原的抗体结合减少,而在麻风分枝杆菌超声裂解物中未减少。提示这是一种具有一个或多个麻风分枝杆菌特异性决定簇的常见分枝杆菌抗原。仅在麻风分枝杆菌超声裂解物中、仅被麻风患者识别出几种抗原:一种12、22、28、36、41和86kD的成分。这些抗原经胰蛋白酶处理后失去抗原性,但具有热稳定性。此类麻风分枝杆菌特异性抗原可能有助于免疫诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/1536007/b11ebf5b19fd/clinexpimmunol00147-0066-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/1536007/c4684c77f855/clinexpimmunol00147-0064-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/1536007/87c77384460a/clinexpimmunol00147-0065-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/1536007/7ec7d00ea186/clinexpimmunol00147-0065-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/1536007/b11ebf5b19fd/clinexpimmunol00147-0066-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/1536007/c4684c77f855/clinexpimmunol00147-0064-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/1536007/87c77384460a/clinexpimmunol00147-0065-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/1536007/7ec7d00ea186/clinexpimmunol00147-0065-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cdb/1536007/b11ebf5b19fd/clinexpimmunol00147-0066-a.jpg

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