4.7 Article

Repurposing Carbamazepine To Treat Gonococcal Infection in Women: Oral Delivery for Control of Epilepsy Generates Therapeutically Effective Levels in Vaginal Secretions

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AMER SOC MICROBIOLOGY
DOI: 10.1128/aac.00968-22

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Neisseria gonorrhoeae; antimicrobial agents; carbamazepine; drug repurposing

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Neisseria gonorrhoeae has developed resistance to previous antibiotics, necessitating the development of novel antimicrobials. Carbamazepine has been shown to block the interaction between gonococcal pili and human complement receptor 3, as well as effectively clear established gonococcal infections. Concentrations of carbamazepine in vaginal fluid from women taking the drug were found to be sufficient to significantly reduce the number of viable gonococci recovered from cervical cell infections. These findings support the further development of carbamazepine as a host-targeted therapy for gonococcal cervicitis.
Neisseria gonorrhoeae has developed resistance to all previous antibiotics used for treatment. This highlights a crucial need for novel antimicrobials to treat gonococcal infections. We previously showed that carbamazepine (Cz), one of the most commonly prescribed antiepileptic drugs, can block the interaction between gonococcal pili and the I-domain region of human complement receptor 3 (CR3)-an interaction that is vital for infection of the female cervix. We also show that Cz can completely clear an established N. gonorrhoeae infection of primary human cervical cells. In this study, we quantified Cz in serum, saliva, and vaginal fluid collected from 16 women who were, or were not, regularly taking Cz. We detected Cz in lower reproductive tract mucosal secretions in the test group (women taking Cz) at potentially therapeutic levels using a competitive ELISA. Furthermore, we found that Cz concentrations present in vaginal fluid from women taking this drug were sufficient to result in a greater than 99% reduction (within 24 h) in the number of viable gonococci recovered from ex vivo, human, primary cervical cell infections. These data provide strong support for the further development of Cz as a novel, host-targeted therapy to treat gonococcal cervicitis.

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