How implementation of systems biology into clinical trials accelerates understanding of diseases

被引:26
作者
Bielekova, Bibiana [1 ,2 ]
Vodovotz, Yoram [3 ,4 ]
An, Gary [4 ,5 ]
Hallenbeck, John [6 ]
机构
[1] NINDS, Neuroimmunol Dis Unit, NIH, Bethesda, MD 20892 USA
[2] NIH, Ctr Human Immunol, Bethesda, MD 20892 USA
[3] Univ Pittsburgh, Dept Surg, Pittsburgh, PA USA
[4] McGowan Inst Regenerat Med, Ctr Inflammat & Regenerat Modeling, Pittsburgh, PA USA
[5] Northwestern Univ, Dept Surg, Chicago, IL 60611 USA
[6] NINDS, Stroke Branch, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
systems biology; clinical trials; clinical trials methodology; multiple sclerosis; polygenic diseases; ENVIRONMENTAL RISK-FACTORS; MULTIPLE-SCLEROSIS; T-CELL; DRUG DISCOVERY; DACLIZUMAB; ACTIVATION; TRANS;
D O I
10.3389/fneur.2014.00102
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Systems biology comprises a series of concepts and approaches that have been used successfully both to delineate novel biological mechanisms and to drive translational advances. The goal of systems biology is to re-integrate putatively critical elements extracted from multi-modality datasets in order to understand how interactions among multiple components form functional networks at the organism/patient-level, and how dysfunction of these networks underlies a particular disease. Due to the genetic and environmental diversity of human subjects, identification of critical elements related to a particular disease process from cross-sectional studies requires prohibitively large cohorts. Alternatively, implementation of systems biology principles to interventional clinical trials represents a unique opportunity to gain predictive understanding of complex diseases in comparatively small cohorts of patients. This paper reviews systems biology principles applicable to translational research, focusing on lessons from systems approaches to inflammation applied to multiple sclerosis. We suggest that employing systems biology methods in the design and execution of biomarker-supported, proof-of-principle clinical trials provides a singular opportunity to merge therapeutic development with a basic understanding of disease processes. The ultimate goal is to develop predictive computational models of the disease, which will revolutionize diagnostic process and provide mechanistic understanding necessary for personalized therapeutic approaches. Added, biologically meaningful information can be derived from diagnostic tests, if they are interpreted in functional relationships, rather than as independent measurements. Such systems biology based diagnostics will transform disease taxonomies from phenotypical to molecular and will allow physicians to select optimal therapeutic regimens for individual patients.
引用
收藏
页数:9
相关论文
共 60 条
[1]   In Silico Augmentation of the Drug Development Pipeline: Examples From the Study of Acute Inflammation [J].
An, Gary ;
Bartels, John ;
Vodovotz, Yoram .
DRUG DEVELOPMENT RESEARCH, 2011, 72 (02) :187-200
[2]   Environmental risk factors for multiple sclerosis. Part II: Noninfectious factors [J].
Ascherio, Alberto ;
Munger, Kassandra L. .
ANNALS OF NEUROLOGY, 2007, 61 (06) :504-513
[3]   Environmental risk factors for multiple sclerosis. Part I: The role of infection [J].
Ascherio, Alberto ;
Munger, Kassandra L. .
ANNALS OF NEUROLOGY, 2007, 61 (04) :288-299
[4]   Dynamics of biological systems: role of systems biology in medical research [J].
Assmus, Heike E. ;
Herwig, Rolf ;
Cho, Kwang-Hyun ;
Wolkenhauer, Olaf .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2006, 6 (06) :891-902
[5]   Systems-based medicine approaches to understand and treat complex diseases. The example of multiple sclerosis [J].
Baranzini, Sergio E. .
AUTOIMMUNITY, 2006, 39 (08) :651-662
[6]   Commensal microbiota and myelin autoantigen cooperate to trigger autoimmune demyelination [J].
Berer, Kerstin ;
Mues, Marsilius ;
Koutrolos, Michail ;
Al Rasbi, Zakeya ;
Boziki, Marina ;
Johner, Caroline ;
Wekerle, Hartmut ;
Krishnamoorthy, Gurumoorthy .
NATURE, 2011, 479 (7374) :538-U266
[7]   Regulatory CD56bright natural killer cells mediate immunomodulatory effects of IL-2Rα-targeted therapy (daclizumab) in multiple sclerosis [J].
Bielekova, B ;
Catalfamo, M ;
Reichert-Scrivner, S ;
Packer, A ;
Cerna, M ;
Waldmann, TA ;
McFarland, H ;
Henkart, PA ;
Martin, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (15) :5941-5946
[8]   Humanized anti-CD25 (daclizumab) inhibits disease activity in multiple sclerosis patients failing to respond to interferon β [J].
Bielekova, B ;
Richert, N ;
Howard, T ;
Blevins, G ;
Markovic-Plese, S ;
McCartin, J ;
Würfel, J ;
Ohayon, J ;
Waidmann, TA ;
McFarland, HF ;
Martin, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (23) :8705-8708
[9]   Intrathecal effects of daclizumab treatment of multiple sclerosis [J].
Bielekova, B. ;
Richert, N. ;
Herman, M. L. ;
Ohayon, J. ;
Waldmann, T. A. ;
McFarland, H. ;
Martin, R. ;
Blevins, G. .
NEUROLOGY, 2011, 77 (21) :1877-1886
[10]   Cellular Pathways of Hereditary Spastic Paraplegia [J].
Blackstone, Craig .
ANNUAL REVIEW OF NEUROSCIENCE, VOL 35, 2012, 35 :25-47