SaBio. Instituto de Investigacion en Recursos Cinegeticos IREC-CSIC-UCLM-JCCM, Ronda de Toledo 12, 13005 Ciudad Real, Spain.
Department of Veterinary Pathobiology, Center for Veterinary Health Sciences, Oklahoma State University, Stillwater, OK 74078, United States.
Curr Med Chem. 2018;25(29):3482-3490. doi: 10.2174/0929867325666180314121813.
Why an autoimmune disease that is the main cause of the acute neuromuscular paralysis worldwide does not have a well-characterized cause or an effective treatment yet? The existence of different clinical variants for the Guillain-Barré syndrome (GBS) coupled with the fact that a high number of pathogens can cause an infection that sometimes, but not always, precedes the development of the syndrome, confers a high degree of uncertainty for both prognosis and treatment. In the post-genomic era, the development of omics technologies for the high-throughput analysis of biological molecules is allowing the characterization of biological systems in a degree of depth unimaginable before. In this context, this work summarizes the application of post-genomics technologies to the study of GBS.
We performed a structured search of bibliographic databases for peer-reviewed research literature to outline the state of the art with regard the application of post-genomics technologies to the study of GBS. The quality of retrieved papers was assessed using standard tools and thirty-four were included in the review. To date, transcriptomics and proteomics have been the unique post-genomics approaches applied to GBS study. Most of these studies have been performed on cerebrospinal fluid samples and only a few studies have been conducted with other samples such as serum, Schwann cells and human peripheral nerve.
In the post-genomics era, transcriptomics and proteomics have shown the possibilities that omics technologies can offer for a better understanding of the immunological and pathological mechanisms involved in GBS and the identification of potential biomarkers, but these results have only shown the tip of the iceberg and there is still a long way to exploit the full potential that post-genomics approaches could offer to the study of the GBS. The integration of different omics datasets through a systems biology approach could allow network-based analyses to describe the complexity and functionality of the molecular mechanisms involved in the course of disease facilitating the discovery of novel biomarkers that could be used to improve the diagnosis, predict the disease progression, improve our understanding of the pathology, and serve as therapeutic targets for GBS.
为什么一种自身免疫性疾病,它是全世界急性神经肌肉瘫痪的主要原因,却没有一个特征明确的病因或有效的治疗方法?格林-巴利综合征(GBS)存在不同的临床变异,而且许多病原体都能引起感染,这种感染有时但并不总是先于综合征的发生,这给预后和治疗带来了高度的不确定性。在后基因组时代,高通量分析生物分子的组学技术的发展使得对生物系统的特征描述达到了以前难以想象的深度。在这种背景下,本工作总结了后基因组技术在 GBS 研究中的应用。
我们对同行评议的研究文献进行了结构化的文献数据库搜索,概述了后基因组技术在 GBS 研究中的应用现状。使用标准工具评估检索到的论文的质量,共纳入 34 篇论文进行综述。迄今为止,转录组学和蛋白质组学是唯一应用于 GBS 研究的后基因组方法。这些研究大多是在脑脊液样本上进行的,只有少数研究是在血清、雪旺细胞和人周围神经等其他样本上进行的。
在后基因组时代,转录组学和蛋白质组学已经显示出组学技术在更好地理解 GBS 中涉及的免疫和病理机制以及识别潜在生物标志物方面所能提供的可能性,但这些结果仅显示出冰山一角,还有很长的路要走,才能充分利用后基因组方法在 GBS 研究中可能提供的全部潜力。通过系统生物学方法整合不同的组学数据集,可以进行基于网络的分析,描述疾病过程中涉及的分子机制的复杂性和功能,从而发现新的生物标志物,这些标志物可用于改善诊断、预测疾病进展、加深对病理学的理解,并作为 GBS 的治疗靶点。