A medicine developed successful nan 1950s to dainty Parkinson's illness whitethorn connection a powerful caller instrumentality successful nan conflict against tuberculosis (TB), according to caller investigation from nan University of British Columbia.
Published in npj Antimicrobials & Resistance, nan study recovered that benztropine, a supplier utilized to negociate tremors successful patients pinch Parkinson's, tin dramatically trim levels of TB-causing germs by boosting nan body's earthy immune response.
TB is nan world's deadliest infectious disease, typically affecting nan lungs and causing an estimated 1.3 cardinal deaths each year. Treatment requires a months-long regimen of aggregate antibiotics, which tin person superior broadside effects and is progressively challenged by nan emergence of drug-resistant bacterial strains.
New approaches for treating tuberculosis are urgently needed. By enhancing immune usability alternatively than targeting nan bacteria, this could beryllium a powerful instrumentality against drug-resistant TB. And, it's a compound that has already proven safe successful group pinch Parkinson's."
Dr. Yossef Av-Gay, elder author, professor of infectious diseases, UBC module of medicine
Tuberculosis is peculiarly difficult to dainty because nan germs responsible, Mycobacterium tuberculosis, is capable to infect and past wrong nan very immune cells designed to destruct pathogens, known arsenic macrophages.
While antibiotics activity by sidesplitting nan germs directly, benztropine functions done an replacement attack that supercharges immune cells to conflict back. The supplier blocks a receptor connected macrophages that TB germs exploit, allowing nan cells to regain their expertise to termination nan bacterial invaders.
The researchers opportunity treatments that heighten nan body's earthy defences, known arsenic host-directed therapies, could connection important benefits successful nan conflict against TB.
"Because these therapies don't straight target nan bacteria, they're acold little apt to thrust supplier resistance," said lead writer Dr. Henok Sahile, a postdoctoral interrogator successful UBC's module of medicine. "They tin besides activity successful operation pinch existing antibiotics to amended curen outcomes aliases thief successful cases wherever antibiotics fail."
To place benztropine, nan investigation squad screened a room of much than 240 U.S. Food and Drug Administration-approved narcotics by testing each compound connected immune cells infected pinch TB.
Benztropine emerged arsenic a standout candidate, tin of importantly reducing TB bacterial counts successful experiments pinch some quality and rodent immune cells. The researchers past tested benztropine successful mice infected pinch TB, pinch oral curen starring to a 70 per cent simplification successful bacterial load successful nan lungs-comparable to immoderate existent TB treatments.
The supplier showed akin effectiveness successful a abstracted rodent exemplary of Salmonella infection, suggesting its imaginable arsenic a curen for a wide scope of pathogens.
Because benztropine is already approved for usage successful humans, nan researchers opportunity nan findings could accelerate its way to objective testing for TB and different infections.
"Repurposing existing narcotics is 1 of nan fastest and astir cost-effective ways to bring caller treatments to patients," said Dr. Av-Gay. "With benztropine, we already understand nan information floor plan and pharmacology, which intends we tin move much quickly toward objective trials."
The interdisciplinary investigation squad progressive microbiologists, immunologists and infectious illness experts astatine UBC's Life Sciences Institute, arsenic good arsenic collaborators astatine nan Vaccine and Infectious Disease Organization astatine nan University of Saskatchewan.
This study was supported by nan Canadian Institutes of Health Research.
Source:
Journal reference:
Sahile, H. A., et al. (2025). The Parkinson’s supplier benztropine possesses histamine receptor 1-dependent host-directed antimicrobial activity against Mycobacterium tuberculosis. npj Antimicrobials and Resistance. doi.org/10.1038/s44259-025-00143-x.