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一种分子定义的皮肤测试试剂,用于诊断牛结核病,与针对约翰氏病的疫苗接种兼容。

A molecularly defined skin test reagent for the diagnosis of bovine tuberculosis compatible with vaccination against Johne's Disease.

机构信息

Animal and Plant Health Agency, Bacteriology, Addlestone, UK.

University College, Dublin, Republic of Ireland.

出版信息

Sci Rep. 2021 Feb 3;11(1):2929. doi: 10.1038/s41598-021-82434-7.

Abstract

Tuberculin Purified Protein Derivatives (PPDs) exhibit multiple limitations: they are crude extracts from mycobacterial cultures with largely unknown active components; their production depends on culture of mycobacteria requiring expensive BCL3 production facilities; and their potency depends on the technically demanding guinea pig assay. To overcome these limitations, we developed a molecularly defined tuberculin (MDT) by adding further antigens to our prototype reagent composed of ESAT-6, CFP-10 and Rv3615c (DIVA skin test, DST). In vitro screening using PBMC from infected and uninfected cattle shortlisted four antigens from a literature-based list of 18 to formulate the MDT. These four antigens plus the previously identified Rv3020c protein, produced as recombinant proteins or overlapping synthetic peptides, were formulated together with the three DST antigens into the MDT to test cattle experimentally and naturally infected with M. bovis, uninfected cattle and MAP vaccinated calves. We demonstrated significant increases in MDT-induced skin responses compared to DST in infected animals, whilst maintaining high specificity in unvaccinated or MAP vaccinated calves. Further, MDT can also be applied in in vitro blood-based interferon-gamma release assays. Thus, MDT promises to be a robust diagnostic skin and blood test reagent overcoming some of the limitations of PPDs and warrants full validation.

摘要

结核菌素纯蛋白衍生物(PPD)存在多种局限性:它们是从分枝杆菌培养物中提取的粗提物,其中活性成分大部分未知;其生产依赖于分枝杆菌的培养,这需要昂贵的 BCL3 生产设施;其效价取决于对豚鼠有技术要求的检测。为了克服这些局限性,我们通过在由 ESAT-6、CFP-10 和 Rv3615c 组成的原型试剂中添加其他抗原,开发了一种分子定义的结核菌素(MDT)(区分免疫和感染皮肤试验,DST)。使用来自感染和未感染牛的 PBMC 进行的体外筛选,从基于文献的 18 种抗原列表中筛选出 4 种抗原,用于构建 MDT。这四种抗原加上之前鉴定的 Rv3020c 蛋白,作为重组蛋白或重叠合成肽生产,与三种 DST 抗原一起配制到 MDT 中,用于对感染了牛分枝杆菌、未感染牛和 MAP 疫苗接种牛的牛进行实验和自然感染测试。与感染动物的 DST 相比,我们证明 MDT 引起的皮肤反应明显增加,同时在未接种或 MAP 疫苗接种的小牛中保持高特异性。此外,MDT 还可以应用于体外基于血液的干扰素-γ释放检测。因此,MDT 有望成为一种强大的诊断皮肤和血液检测试剂,克服了 PPD 的一些局限性,值得进行全面验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dda0/7859399/63fada108082/41598_2021_82434_Fig1_HTML.jpg

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