Computational modeling of tuberculous meningitis reveals an important role for tumor necrosis factor-alpha
Authored by Denise E Kirschner, M. El-Kebir, M. van der Kuip, A. M. van Furth
Date Published: 2013-07-07
DOI: 10.1016/j.jtbi.2013.03.008
Sponsors:
United States National Institutes of Health (NIH)
Platforms:
C++
Model Documentation:
Other Narrative
Flow charts
Pseudocode
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Model code not found
Abstract
Tuberculosis is a global health issue with annually about 1.5 million deaths and 2 billion infected people worldwide. Extra-pulmonary tuberculosis comprises 13% of all cases of which tuberculous meningitis is the most severe. It has a high mortality and is often diagnosed once irreversible neurological damage has already occurred. Development of diagnostic and treatment strategies requires a thorough understanding of the pathogenesis of tuberculous meningitis. This disease is characterized by the formation of a cerebral granuloma, which is a collection of immune cells that attempt to immunologically restrain, and physically contain bacteria. The cytokine tumor necrosis factor-a is known for its important role in granuloma formation. Because traditional experimental animal studies exploring tuberculous meningitis are difficult and expensive, another approach is needed to begin to address this important and significant disease outcome. Here, we present an in silico model capturing the unique immunological environment of the brain that allows us to study the key mechanisms driving granuloma formation in time. Uncertainty and sensitivity analysis reveals a dose-dependent effect of tumor necrosis factor-a on bacterial load and immune cell numbers thereby influencing the onset of tuberculous meningitis. Insufficient levels result in bacterial overgrowth, whereas high levels lead to uncontrolled inflammation being detrimental to the host. These findings have important implications for the development of immuno-modulating treatment strategies for tuberculous meningitis. (C) 2013 Elsevier Ltd. All rights reserved.
Tags
Agent based model
Granuloma formation
Central nervous system
Rich focus
Tumor necrosis factor