Investigating tuberculosis pathology in the human lung with 3D X-ray Histology; a correlative imaging approach

Dr. Eleni Konstantinopoulou1, Dr. Orestis Katsamenis2, Dr. Sanjay Jogai3, Dr. David Chatelet4, Dr. Matthew Lawson1, Dr. Philip Basford5, Elaine Ho6, Prof. Philipp Schneider2,6,7, Prof. Paul Elkington1

1 Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom

2 µ-VIS X-ray Imaging Centre, Faculty of Engineering and Physical Sciences, University of Southampton, Southampton, United Kingdom

3 University Hospital Southampton, NHS National Health Service, Southampton, United Kingdom

4 Biomedical Imaging Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom

5 Computational Engineering and Design, Faculty of Engineering and Physical Sciences, University of Southampton, Southampton, United Kingdom

6 Bioengineering Science Research Group, Faculty of Engineering and Physical Sciences, University of Southampton, Southampton, United Kingdom

7 High-Performance Vision Systems, Center for Vision, Automation & Control, AIT Austrian Institute of Technology, Vienna, Austria

Abstract

Tuberculosis kills more than 1.5 million people every year. (1) Most studies on tuberculosis use either animal or in vitro cell culture models that do not recapitulate human disease. The most common method of disease investigation (used in both research and clinical workflows) is the route of traditional histology, which involves thinly sectioning the sample and chemically staining said sections to extract specific molecular/cellular information about the tissue. However, such two-dimensional systems present with limitations regarding tissue connectivity and three-dimensionality of tissue structures. Consequently, fundamental mechanisms in human tuberculosis disease are poorly understood. (2-6)

In this project, we have developed a correlative imaging approach by integrating non-invasive 3D micro-CT imaging (7-9) with traditional 2D histology of formalin-fixed paraffin-embedded (FFPE) human lung biopsies from tuberculosis patients. We leverage the third dimension added to our histology imaging data by micro-CT to explore disease process in tuberculosis, interrogating the structure of tuberculous granulomas and the interconnectivity of tissue microenvironments which is lost when imaging representative 2D sections by traditional optical microscopy.

Human tuberculous lung biopsies were first imaged with micro-CT. The FFPE biopsies were then thinly sectioned and each section was stained with either histological or tinctorial stains to reveal areas of tuberculous pathology, fibrosis and calcification. Sections were scanned using a slide-scanner and optical microscopy. Manual segmentation in 3D was based on annotations performed by a consultant histopathologist on the digital histology slides. Preliminary data suggests that these analyses will provide unique insight into human disease and the interrelationships of microenvironments in 3D.

References:

(1) Global tuberculosis report 2020, World Health Organization (WHO), 2020, ISBN 978-92-4-001313-1

(2) O’Garra A, Redford PS, McNab FW, et al. The immune response in tuberculosis. Annual Review of Immunology. 2013;31:475-527; DOI: 10.1146/annurev-immunol-032712-095939

(3) Bielecka MK, Tezera LB, Zmijan R, et al. A Bioengineered Three-Dimensional Cell Culture Platform Integrated with Microfluidics To Address Antimicrobial Resistance in Tuberculosis. MBio 2017;8(1):e02073-16; DOI: 10.1128/mBio.02073-16

(4) Tezera LB, Bielecka MK, Chancellor A, et al. Dissection of the host-pathogen interaction in human tuberculosis using a bioengineered 3-dimensional model. eLife 2017;6:e21283; DOI: 10.7554/eLife.21283

(5) Workman VL, Tezera LB, Elkington PT, et al. Controlled Generation of Microspheres Incorporating Extracellular Matrix Fibrils for Three-Dimensional Cell Culture. Advanced Functional Materials 2014;24(18):2648-57; DOI: 10.1002/adfm.201303891

(6) Tezera LB, Bielecka MK, Ogongo P, et al. Anti-PD-1 immunotherapy leads to tuberculosis reactivation via dysregulation of TNF-α. eLife 2020;9:e52668; DOI: 10.7554/eLife.52668

(7) Katsamenis OL, Olding M, Warner JA, et al. X-ray micro-computed tomography for non-destructive 3D X-ray histology. The American journal of pathology. 2019.05.004; DOI: 10.1016/j.ajpath.2019.05.004

(8) Wollatz L, Johnston SJ, Lackie PM, et al. 3D Histopathology—a Lung Tissue Segmentation Workflow for Microfocus X-ray-Computed Tomography Scans. Journal of Digital Imaging. 2017;1-10; DOI: 10.1007/s10278-017-9966-5

(9) Koo H-K, Vasilescu DM, Booth S, et al. Small airways disease in mild and moderate chronic obstructive pulmonary disease: a cross-sectional study. The Lancet, Respiratory medicine. 2018;6:591-602; DOI: 10.1016/S2213-2600(18)30196-6

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