TB is an air-borne infectious disease caused by a bacterium called Mycobacterium Tuberculosis (Mtb), which often infects the lungs.
Even though drugs are available to treat the disease, TB continues to be a major threat to public health, killing close to 1.5 million people every year.
Conventional drugs used to treat TB usually adopt a pathogen-targeted strategy which attacks and kills bacteria directly.
This approach has caused Mtb strains to acquire drug resistance, making existing treatments become increasingly ineffective and resulting in a pressing need to design new therapeutic strategies for the disease.
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They screened FDA-approved drugs and identified Metformin (MET), an old anti-diabetic drug that could defend Mtb invasion without targeting the bacteria directly.
Instead, MET targets the host cells to trigger the production of a chemical which then damages Mtb and stops its replication.
Such indirect, host-targeted approach is less likely to engender drug resistance. The team also discovered that MET improves the efficacy of conventional anti-TB drugs when used in combination with them.
This anti-diabetic drug is therefore a promising adjunctive therapy that could enhance the effectiveness of existing TB treatments.
As it is a drug that is currently in use, another benefit of using MET as an adjunct treatment for TB is that it is likely to shorten the time required for clinical trials.
"Using MET as an adjunct treatment for TB is very promising since this drug interferes with the biochemical pathway essential for the bacteria's survival and does not promote the development of drug resistance," said lead scientists Dr Amit Singhal, Project Leader and Prof Gennaro De Libero, Principal Investigator at SIgN.