T7噬菌体展示库是检测结核病特异性生物标志物的一种有前途的策略。

H. Talwar, J. Talreja, L. Samavati
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引用次数: 9

摘要

世界上三分之一的人口感染结核病,只有10%会发展为活动性疾病,其余90%被认为是潜伏性结核病(LTB)。虽然活动性结核病具有传染性并可能致命,但LTB可以演变为活动性结核病。结核病的诊断可能具有挑战性,特别是在早期阶段,因为表现和非特异性体征和症状存在差异。目前,我们只有有限的工具来诊断活动性结核病,预测活动性结核病的治疗效果和治愈,潜伏性结核感染的再激活,以及通过疫苗接种诱导保护性免疫反应。因此,鉴定强大而准确的结核病特异性生物标志物对于成功根除结核病至关重要。在这篇评论中,我们总结了现有的诊断和鉴别活动性结核和LTB的方法及其局限性。此外,我们提出了一种新的肽微阵列平台,作为识别结核病生物标志物的有希望的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
T7 Phage Display Library a Promising Strategy to Detect Tuberculosis Specific Biomarkers.
One-third of the world's population is infected with tuberculosis, only 10% will develop active disease and the remaining 90% is considered to have latent TB (LTB). While active TB is contagious and can be lethal, the LTB can evolve to active TB. The diagnosis of TB can be challenging, especially in the early stages, due to the variability in presentation and nonspecific signs and symptoms. Currently, we have limited tools available to diagnose active TB, predict treatment efficacy and cure of active tuberculosis, the reactivation of latent tuberculosis infection, and the induction of protective immune responses through vaccination. Therefore, the identification of robust and accurate tuberculosis-specific biomarkers is crucial for the successful eradication of TB. In this commentary, we summarized the available methods for diagnosis and differentiation of active TB from LTB and their limitations. Additionally, we present a novel peptide microarray platform as promising strategy to identify TB biomarkers.
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