Suppr超能文献

评价用于诊断人类丝虫病的 WbSXP-1 合成肽。

Evaluation of synthetic peptides of WbSXP-1 for the diagnosis of human lymphatic filariasis.

机构信息

Centre for Biotechnology, Anna University, Chennai, Tamil Nadu, India.

出版信息

Diagn Microbiol Infect Dis. 2010 Dec;68(4):410-5. doi: 10.1016/j.diagmicrobio.2010.07.015.

Abstract

Parasitic nematodes infect nearly half of the world's human population, resulting in significant morbidity and mortality. Though filariasis is not fatal, it is the second leading cause of permanent and long-term disability worldwide. Filariasis has a spectrum of disease manifestation and infectivity found among the infected individuals and also goes unnoticed for years. Furthermore, there are ample reports emerging on the genetic variation among the parasites population. Hence, it is necessary to develop diagnostics for early detection of the disease. Synthetic peptides that mimic the immunogenic regions and a conserved region similar to that of recombinant antigen will be more useful in developing diagnostics, vaccines, or therapeutics. WbSXP-1 was earlier proven as a good diagnostic antigen; B-cell epitopic analysis showed 4 potent immunodominant regions spanning the whole antigen. These synthetic peptides (N, N1, N2, and N3) were produced and used as a diagnostic candidate to detect anti-SXP antibody and conversely to detect the infected individuals. The monomeric peptides showed good reactivity against microfilareamic (MF) sera. Among them, the peptides N, N1, and N2 were found to be more reactive. Furthermore, multiple chimeric peptides in linear combinations of 2 peptides were tested for its efficacy to detect anti-SXP antibody in infected MF sera. The peptides N:N1 and N1:N2 were synthesized and tested against human clinical sera. This chimeric peptides constructed based on WbSXP-1 were found to be reactive, specifically with MF sera by ELISA. These peptide-based diagnostic method can serve as a standard better tool without cross-reactivity in lymphatic filariasis elimination program.

摘要

寄生虫线虫感染了全球近一半的人口,导致了严重的发病率和死亡率。尽管丝虫病不会致命,但它是全球第二大致残和长期残疾的主要原因。丝虫病在受感染个体中具有一系列的疾病表现和传染性,并且多年来未被发现。此外,寄生虫群体中的遗传变异也有大量报道。因此,有必要开发用于早期检测疾病的诊断方法。模拟免疫原性区域和与重组抗原相似的保守区域的合成肽在开发诊断、疫苗或治疗方法方面将更加有用。WbSXP-1 早些时候已被证明是一种很好的诊断抗原;B 细胞表位分析显示了跨越整个抗原的 4 个强大的免疫显性区域。这些合成肽(N、N1、N2 和 N3)被生产并用作诊断候选物,以检测针对 SXP 的抗体,反之亦然,以检测受感染的个体。单体肽对微丝蚴血症(MF)血清显示出良好的反应性。其中,肽 N、N1 和 N2 反应性更强。此外,还测试了线性组合 2 个肽的多个嵌合肽,以评估其在感染 MF 血清中检测针对 SXP 的抗体的效果。肽 N:N1 和 N1:N2 被合成并针对人临床血清进行了测试。通过 ELISA 发现,这些基于 WbSXP-1 构建的嵌合肽具有反应性,特别是对 MF 血清具有反应性。这些基于肽的诊断方法可以作为一种更好的标准工具,在淋巴丝虫病消除计划中没有交叉反应。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验