Sensitivity analysis of an ENteric immunity SImulator (ENISI)-based model of immune responses to Helicobacter pylori infection

Maksudul Alam, Xinwei Deng, Casandra Philipson, Josep Bassaganya-Riera, Keith Bisset, Adria Carbo, Stephen Eubank, Raquel Hontecillas, Stefan Hoops, Yongguo Mei, Vida Abedi, Madhav Marathe

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Agent-based models (ABM) are widely used to study immune systems, providing a procedural and interactive view of the underlying system. The interaction of components and the behavior of individual objects is described procedurally as a function of the internal states and the local interactions, which are often stochastic in nature. Such models typically have complex structures and consist of a large number of modeling parameters. Determining the key modeling parameters which govern the outcomes of the system is very challenging. Sensitivity analysis plays a vital role in quantifying the impact of modeling parameters in massively interacting systems, including large complex ABM. The high computational cost of executing simulations impedes running experiments with exhaustive parameter settings. Existing techniques of analyzing such a complex system typically focus on local sensitivity analysis, i.e. one parameter at a time, or a close "neighborhood" of particular parameter settings. However, such methods are not adequate to measure the uncertainty and sensitivity of parameters accurately because they overlook the global impacts of parameters on the system. In this article, we develop novel experimental design and analysis techniques to perform both global and local sensitivity analysis of large-scale ABMs. The proposed method can efficiently identify the most significant parameters and quantify their contributions to outcomes of the system. We demonstrate the proposed methodology for ENteric Immune SImulator (ENISI), a large-scale ABM environment, using a computational model of immune responses to Helicobacter pylori colonization of the gastric mucosa.

Original languageEnglish
Article numbere0136139
JournalPLoS ONE
Volume10
Issue number9
DOIs
StatePublished - Sep 1 2015
Externally publishedYes

Funding

We thank our external collaborators and members of the Network Dynamics and Simulation Science Laboratory (NDSSL) and the Nutritional Immunology and Molecular Medicine Laboratory (NIMML, http://www.nimml.org ) for their suggestions and comments. This work has been partially supported by Defense Threat Reduction Agency (DTRA)—R&D (HPC) Award No. HDTRA1-09-1-0017, DTRA—Validation Award No. HDTRA1-11-1-0016, DTRA—Comprehensive National Incident Management System (CNIMS) Award No. HDRTA1-11-D-0016-0001, National Science Foundation (NSF) PetaApps Grant OCI-0904844, NSF Network Science and Engineering (NetSE) Grant CNS-1011769, NSF Software Development for Cyberinfrastructure (SDCI) Grant OCI-1032677, National Institutes of Health (NIH) MIDAS project 2U01GM070694-7 and National Institute of Allergy and Infectious Diseases (NIAID) & NIH project HHSN272201000056C.

FundersFunder number
NSF Network Science and Engineering
NSF Software Development for Cyberinfrastructure
National Institute of Allergy and Infectious Diseases
National Institutes of Health
NetSECNS-1011769
SDCIOCI-1032677
National Science FoundationOCI-0904844
National Institutes of Health
National Institute of General Medical SciencesU01GM070694
National Institute of Allergy and Infectious DiseasesHHSN272201000056C
Defense Threat Reduction AgencyHDRTA1-11-D-0016-0001, HDTRA1-09-1-0017, HDTRA1-11-1-0016

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