In the first of a Series of three papers published in The Lancet Respiratory Medicine and eBioMedicine, Keertan Dheda and colleagues
discuss the effects of COVID-19 on efforts to end tuberculosis and the need for wide-ranging interventions to restore tuberculosis control, including the need to implement and enhance tuberculosis diagnostic tests to reduce under-diagnosis. In the second paper, Ruvandhi Nathavitharana and colleagues
highlight progress in the development of non-sputum-based diagnostic tests with potential for decentralised deployment. Finally, Hanif Esmail and colleagues
discuss optimal treatment regimens across the full spectrum of tuberculosis infection and tuberculosis disease, previously known as latent tuberculosis and active tuberculosis, respectively.
Although these articles apply mainly to pulmonary tuberculosis, advances in the diagnosis and treatment of extrapulmonary tuberculosis will have to be made concurrently in addressing the substantial burden of disease. Importantly, the various sequelae after tuberculosis need to be understood and optimally managed.
Finally, options for the prevention of tuberculosis in the form of robust vaccines need to be developed.
Translational research will underpin progress in preventing and managing the entire spectrum of tuberculosis, and a pressing need exists for investment and support to strengthen research capacity.
highlight the need to develop a sensitive and specific, rapid, non-sputum-based tuberculosis test by harnessing existing resources invested in COVID-19 detection. By use of easily accessible clinical samples, such as urine or oral swabs for diagnosis and implementing point-of-care tests, tuberculosis diagnosis could be enhanced in LMICs, where the majority of the world's tuberculosis burden is found.
Such diagnostic tests need to be broadly applicable to all population types, including immunocompromised individuals, who tend to have atypical presentations and are often sputum-smear negative, which compromises the yield of the more rapid nucleic-acid tests.
Additionally, the performance of existing tuberculosis nucleic-acid tests is variable across specimen types, which is less than ideal and underscores the need for better diagnostic tests. The gold-standard tuberculosis cultures and drug-susceptibility tests remain unavailable in most LMICs, but the advent of whole-genome sequencing shortens the time to determine anti-tuberculosis drug susceptibility for more effective tuberculosis treatment.
Such technology, if made available across resource settings, would help to stem transmission of both drug-susceptible and drug-resistant Mycobacterium tuberculosis because it allows prompt initiation of effective anti-tubercular treatment.
propose an approach in which tuberculosis treatment and management are tailored across the tuberculosis spectrum, instead of being provided within the binary framework of tuberculosis infection and tuberculosis disease. However, extensive work is needed before this concept can be realised in clinical practice. For example, the implementation of this concept requires the development of a host-based or mycobacteria-based biomarker that indicates eradication of the pathogen, applicable to both tuberculosis infection and disease states of pulmonary and extrapulmonary tuberculosis, regardless of the level of immunity. Once validated in several independent cohorts, this biomarker would be useful in guiding the duration of treatment for infection or disease. Drug discovery and repurposing of drugs takes an excruciatingly long time in the tuberculosis field, but scientific and political will can remove barriers and expedite the process, similar to progress observed in COVID-19, with the necessary funding.
before studies in humans in phase 2 and 3 clinical trials.
but the extent of the global burden of lung disease after tuberculosis infection is poorly defined and likely to be under-reported. Mechanisms that underlie tuberculosis tissue destruction and fibrosis are being established. Phase 2 clinical trials repurposing existing drugs, such as doxycycline and everolimus, to decrease tissue destruction hold promise in improving lung function and ameliorating sequelae from post-tuberculosis lung disease,
but their efficacy would need to be demonstrated in larger cohorts before being implemented in practice. These measures, together with measures such as pulmonary rehabilitation, need to be adopted according to an agreed clinical standard to reduce the global burden of tuberculosis sequelae.
Altogether, tuberculosis translational research remains key to advancing prevention and management across the entire spectrum of tuberculosis, which is still a leading killer globally. Despite the catastrophic setbacks from COVID-19, researchers need to continue to push ahead to reach the ultimate goal of ending tuberculosis. As has been seen for COVID-19, a whole-of-government approach for tuberculosis is needed for the development of effective diagnostic and treatment approaches to stem transmission and save lives.
CWMO has received speaking fees from Qiagen, outside this work. The other authors declare no competing interests.
Table of Contents
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Gauging the impact of the COVID-19 pandemic on tuberculosis services: a global study.
Eur Respir J. 2021; 582101786
The intersecting pandemics of tuberculosis and COVID-19: population-level and patient-level impact, clinical presentation, and corrective interventions.
Lancet Respir Med. 2022; ()
Reimagining the status quo: how close are we to rapid sputum-free tuberculosis diagnostics for all?.
EBioMedicine. 2022; ()
Mind the gap – managing tuberculosis across the disease spectrum.
EBioMedicine. 2022; ()
Clinical standards for the assessment, management and rehabilitation of post-TB lung disease.
Int J Tuberc Lung Dis. 2021; 25: 797-813
Accelerating research and development of new vaccines against tuberculosis: a global roadmap.
Lancet Infect Dis. 2022; ()
Lack of latent tuberculosis (TB) screening and delay in anti-retroviral therapy initiation in HIV-TB co-infection: an 11-year study in an intermediate TB-burden country.
Int J Infect Dis. 2021; 113: 178-183
Prediction of susceptibility to first-line tuberculosis drugs by DNA Sequencing.
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The scientific response to TB — the other deadly global health emergency.
Int J Tuberc Lung Dis. 2022; 26: 186-189
Nos2−/− mice infected with M. tuberculosis develop neurobehavioral changes and immunopathology mimicking human central nervous system tuberculosis.
J Neuroinflammation. 2022; 19: 21
Pulmonary tuberculosis treated with directly observed therapy: serial changes in lung structure and function.
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Doxycycline host-directed therapy in human pulmonary tuberculosis.
J Clin Invest. 2021; 131e141895
Adjunctive host-directed therapies for pulmonary tuberculosis: a prospective, open-label, phase 2, randomised controlled trial.
Lancet Respir Med. 2021; 9: 897-908
Published: March 23, 2022
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