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Purpose Of Review: Pregnant people living with HIV (PLWH) are at especially high risk for progression from latent tuberculosis infection (LTBI) to active tuberculosis (TB) disease. Among pregnant PLWH, concurrent TB increases the risk of complications such as preeclampsia, intrauterine fetal-growth restriction, low birth weight, preterm-delivery, perinatal transmission of HIV, and admission to the neonatal intensive care unit. The grave impact of superimposed TB disease on maternal morbidity and mortality among PLWH necessitates clear guidelines for concomitant therapy and an understanding of the pharmacokinetics (PK) and potential drug-drug interactions (DDIs) between antitubercular (anti-TB) agents and antiretroviral therapy (ART) in pregnancy.
Recent Findings: This review discusses the currently available evidence on the use of anti-TB agents in pregnant PLWH on ART. Pharmacokinetic and safety studies of anti-TB agents during pregnancy and postpartum are limited, and available data on second-line and newer anti-TB agents used in pregnancy suggest that several research gaps exist. DDIs between ART and anti-TB agents can decrease plasma concentration of ART, with the potential for perinatal transmission of HIV. Current recommendations for the treatment of LTBI, drug-susceptible TB, and multidrug-resistant TB (MDR-TB) are derived from observational studies and case reports in pregnant PLWH. While the use of isoniazid, rifamycins, and ethambutol in pregnancy and their DDIs with various ARTs are well-characterized, there is limited data on the use of pyrazinamide and several new and second-line antitubercular drugs in pregnant PLWH. Further research into treatment outcomes, PK, and safety data for anti-TB agent use during pregnancy and postpartum is urgently needed.
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http://dx.doi.org/10.1007/s11904-022-00641-x | DOI Listing |
Clin Exp Med
August 2025
Department of pathology, College of Medicine, King Khalid University, Abha, Saudi Arabia.
This study examined the association between diabetes mellitus and tuberculosis (TB) in a cohort of 200TB-positive patients, stratified by gender, age, treatment regimen, and comorbidities, including diabetes, acute gastroenteritis, and hypertension, compared to TB patients without additional complications. Clinical parameters-Random Blood Sugar (RBS), C-reactive protein (CRP), and Erythrocyte Sedimentation Rate (ESR)-were assessed at baseline and after four months of anti-TB therapy. The results showed no significant changes in mean RBS or CRP levels post-treatment, but a notable reduction in mean ESR was observed.
View Article and Find Full Text PDFEur J Pharmacol
August 2025
National Clinical Research Center for Infectious Diseases, Shenzhen Third People's Hospital, Shenzhen, Guangdong, China. Electronic address:
The increasing prevalence of drug-resistant tuberculosis (TB), coupled with the lengthy and toxic nature of conventional treatments and the complicating factor of Human Immunodeficiency Virus (HIV) co-infection, underscores the urgent need for the development of effective anti-TB drugs and robust stockpiles to combat this global health crisis. In this study, the anti-tubercular activity and potential antibacterial mechanisms of tioconazole were investigated. Tioconazole exhibited remarkable antibacterial activity against Mtb H37Ra and H37Rv, with minimum inhibitory concentrations (MICs) of 4 μg/mL and 1 μg/mL respectively.
View Article and Find Full Text PDFSci Rep
August 2025
Quality assurance and enhancement directorate, College of Medicine and Health Sciences, Wachemo University, Hosaina, Ethiopia.
Tuberculosis (TB) is a curable disease that can be treated with antitubercular (anti-TB) drugs that have markedly reduced mortality due to the disease. However, the drugs may cause liver injury, which is associated with increased morbidity due to acute liver failure, disease progression, and drug resistance. There is a scarcity of evidence on the prevalence and predictors of anti-TB drug-induced liver injury (ATDILI).
View Article and Find Full Text PDFJ Med Chem
August 2025
Department of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Balanagar, Hyderabad, Telangana 500037, India.
The alarming rise of multidrug-resistant tuberculosis (MDR-TB) underscores the urgent need for new classes of antitubercular agents targeting novel pathways. To address this, a series of indole triazole sulfonamides were rationally designed, incorporating an indole pharmacophore hybridized with a triazole linker containing a sulfonamide group. Compound had the highest anti-TB efficacy against with a MIC of 0.
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