A computational model to understand the dynamics of tuberculosis lesions within the lungs

A computational model to understand the dynamics of tuberculosis lesions within the lungs
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Representation of lesion evolution

A computational model to understand the dynamics of tuberculosis lesions within the lungs
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Computational minipig bronchial tree

Researchers from the UPC and the Institut Germans Trias i Pujol (IGTP) have developed a virtual lung model using computational modelling techniques to study the dynamics of tuberculosis lesions within the lungs. These are the first results to be published by the 3Rs Programme at the Centre for Comparative Medicine and Bioimaging (CMCiB), which aims to minimize the use of animals in preclinical research. The results of the study have been published in the journal Plos Computational Biology.

Oct 09, 2020

The researchers of the Experimental Tuberculosis Unit of the Germans Trias i Pujol Research Institute (IGTP), led by Pere-Joan Cardona, have published the first results of a computational model that aims to reproduce the dynamics of tuberculosis lesions in a virtual lung. The model has been developed within the 3Rs Programme of the Centre for Comparative Medicine and Bioimaging (CMCiB) of the IGTP, supported by the ”la Caixa” Foundation. Martí Català and Clara Prats, researchers from the Department of Physics of the Universitat Politècnica de Catalunya · BarcelonaTech (UPC) at the CMCiB, and Daniel López-Codina, Sergio Alonso and Joaquim Valls, who are also UPC researchers, took part in the study. Català, the first author of the paper, led the in silico trial of the programme. Its results have been published in the journal Plos Computational Biology.

Today tuberculosis (TB) is still among the world’s top 10 causes of death, having killed 1.6 million people in 2017. Tuberculosis is caused by Mycobacterium tuberculosis, a bacterium that infects pulmonary alveoli. However, 90% of people will never develop the active disease. Not knowing the main factors that trigger the disease in the remaining 10% of cases is one of the main obstacles to its eradication. This study aims to understand the mechanisms that allow the disease to remain latent, especially those related to endogenous reinfection.

The researchers have started from the hypothesis that endogenous reinfection plays an important role in maintaining latent infection. “So, we have developed an agent-based model that describes the growth, fusion and proliferation of tuberculosis lesions in a computational bronchial tree, built from an iterative algorithm that generates bronchial tubes and bifurcations within a 3D volume of the lung surface area”, explains Clara Prats, a researcher at the UPC’s Department of Physics and a member of the Computational Biology and Complex Systems Group. The model has been fed and set up using experimental data from computed tomography scans of five minipigs in the initial stages of infection. The lung surface area of the minipigs has been obtained from these images in order to generate the computational lung. The size and location of each of the TB lesions has also been obtained, which has allowed the researchers to set the parameters of the agent-based model. “The result is a model that allows us to reproduce and understand the experimental data on the computer. We have been able to show an important relationship between the final number of tuberculosis lesions and the frequency of endogenous reinfection and lesion growth”, adds Martí Català.

The model has also been used as an in silico experimental platform to explore the transition from latent infection to active disease, identifying the main triggers: an elevated inflammatory response and the combination of a moderate inflammatory response with low respiratory amplitude. “This study is important because the lung structure of minipigs is very similar to that of humans, so that this model will allow us to make predictions for future actions such as new biomarkers, preventive strategies and therapies for tuberculosis in humans”, explains Pere-Joan Cardona, the co-author of the project.

In silico or computational models
The use of animal models, known as comparative medicine, has been one of the main keys to the huge developments in medicine in the 20th century and particularly in research in the fields of health and life sciences. It remains a necessary and mandatory step for research in these fields, especially for developing new treatments and drugs. New technologies have allowed for the refinement of this practice, which is the main purpose of the research facilities and projects at the Centre for Comparative Medicine and Bioimaging (CMCiB). The Centre promotes research based on the 3Rs: replace, reduce and refine. The use of computational tools for simulation, such as in this case, is a clear example. “Less is more in comparative medicine. Our group has been using alternative models for many years in preclinical research, such as the Drosophila model for tuberculosis research, a paradigmatic example. Now the possibilities offered by computer-generated models are enormous”, explains Cardona, the principal investigator of the Experimental Tuberculosis Unit and the scientific director of the CMCiB. “In this case we have obtained reliable results by generating a model using a small number of animals and bioimaging tools. Now we will not need more animals, the model is in the computer and we will be able to use it for many future studies”, he adds.

These are the first results published within the framework of the 3Rs Programme at the CMCiB, which is supported by the ”la Caixa” Foundation. Other projects are also underway on tuberculosis, ictus, computational models for HIV vaccines and new therapeutic targets in acute leukaemia.