The Francis Crick Institute
lanni-et-al-2023-a-preclinical-model-of-tb-meningitis-to-determine-drug-penetration-and-activity-at-the-sites-of-disease (1).pdf (1.08 MB)

A preclinical model of TB meningitis to determine drug penetration and activity at the sites of disease.

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journal contribution
posted on 2024-01-10, 11:27 authored by Faye Lanni, Rosleine Antilus Sainte, Mark Hansen Jr., Paul Parigi, Firat Kaya, Katherine LoMauro, Bernard Siow, Robert J Wilkinson, Sean Wasserman, Brendan K Podell, Martin Gengenbacher, Véronique Dartois
Tuberculosis meningitis (TBM) is essentially treated with the first-line regimen used against pulmonary tuberculosis, with a prolonged continuation phase. However, clinical outcomes are poor in comparison, for reasons that are only partially understood, highlighting the need for improved preclinical tools to measure drug distribution and activity at the site of disease. A predictive animal model of TBM would also be of great value to prioritize promising drug regimens to be tested in clinical trials, given the healthy state of the development pipeline for the first time in decades. Here, we report the optimization of a rabbit model of TBM disease induced via inoculation of Mycobacterium tuberculosis into the cisterna magna, recapitulating features typical of clinical TBM: neurological deterioration within months post-infection, acid-fast bacilli in necrotic lesions in the brain and spinal cord, and elevated lactate levels in cerebrospinal fluid (CSF). None of the infected rabbits recovered or controlled the disease. We used young adult rabbits, the size of which allows for spatial drug quantitation in critical compartments of the central nervous system that cannot be collected in clinical studies. To illustrate the translational value of the model, we report the penetration of linezolid from plasma into the CSF, meninges, anatomically distinct brain areas, cervical spine, and lumbar spine. Across animals, we measured the bacterial burden concomitant with neurological deterioration, offering a useful readout for drug efficacy studies. The model thus forms the basis for building a preclinical platform to identify improved regimens and inform clinical trial design.


Crick (Grant ID: 10020, Grant title: STP BRF - In Vivo Imaging) Crick (Grant ID: CC1109, Grant title: STP BRF) Crick (Grant ID: CC2112, Grant title: Wilkinson CC2112)