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伤寒沙门氏菌O:9,12多糖-蛋白结合物:与混合及个体正常人血清、甲型和乙型副伤寒及伤寒患者血清以及动物血清的特性及免疫反应性

Salmonella typhi O:9,12 polysaccharide-protein conjugates: characterization and immunoreactivity with pooled and individual normal human sera, sera from patients with paratyphoid A and B and typhoid fever, and animal sera.

作者信息

Aron L, Di Fabio J, Cabello F C

机构信息

Department of Microbiology and Immunology, New York Medical College, Valhalla 10595.

出版信息

J Clin Microbiol. 1993 Apr;31(4):975-8. doi: 10.1128/jcm.31.4.975-978.1993.

DOI:10.1128/jcm.31.4.975-978.1993
PMID:7681853
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC263597/
Abstract

Polysaccharide of O:9,12 specificity purified from Salmonella typhi was conjugated to tetanus toxoid or bovine serum albumin in order to obtain defined antigenic material that would contain O chain free of other S. typhi antigens and that would be suitable for characterizing host humoral response to only S. typhi O-chain antigens. These artificial conjugates were strongly reactive in immunodots with 18 pooled and 3 individual serum samples from patients with typhoid fever and with rabbit anti-Salmonella O antiserum (group D, factors 1, 9, and 12). They reacted weakly with one serum sample from one human with paratyphoid A. These results suggest that the periodate oxidation and the reductive amination used in the conjugation conserved the immunogenicity of the O chain and allowed its absorption to nitrocellulose. They also suggest that the bovine serum albumin conjugate could be used in the diagnosis of S. typhi infections as normal sera may react with the protein molecule of the tetanus toxoid conjugate.

摘要

从伤寒沙门氏菌中纯化出具有O:9,12特异性的多糖,并将其与破伤风类毒素或牛血清白蛋白偶联,以获得特定的抗原物质,该物质将包含不含其他伤寒沙门氏菌抗原的O链,并且适合于表征宿主对仅伤寒沙门氏菌O链抗原的体液免疫反应。这些人工偶联物在免疫斑点试验中与18份来自伤寒热患者的混合血清样本和3份个体血清样本以及兔抗沙门氏菌O抗血清(D组,因子1、9和12)有强烈反应。它们与1例副伤寒A患者的1份血清样本反应较弱。这些结果表明,偶联过程中使用的高碘酸盐氧化和还原胺化保留了O链的免疫原性,并使其能吸附到硝酸纤维素上。它们还表明,牛血清白蛋白偶联物可用于伤寒沙门氏菌感染的诊断,因为正常血清可能会与破伤风类毒素偶联物的蛋白质分子发生反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f2/263597/c9fd6df99a54/jcm00016-0225-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f2/263597/e1272211259e/jcm00016-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f2/263597/f7b55265fd44/jcm00016-0224-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f2/263597/c9fd6df99a54/jcm00016-0225-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f2/263597/e1272211259e/jcm00016-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f2/263597/f7b55265fd44/jcm00016-0224-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f2/263597/c9fd6df99a54/jcm00016-0225-a.jpg

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