Topic Editors

Departamento de Ciências Biológicas, São Paulo State University, Sao Paulo, Brazil
Centro de Ciências Exatas e de Tecnologia (CCET), Universidade Federal de São Carlos, Sao Carlos, Brazil
Dr. Adelino Vieira de Godoy Netto
Instituto de Química, São Paulo State University, Sao Paulo, Brazil
Núcleo de Desenvolvimento de Novos Fármacos (NUDEFA), Rio Grande Federal University, Rio Grande, Brazil

Research for New Drugs against Tuberculosis and Other Mycobacterial Diseases

Abstract submission deadline
31 May 2023
Manuscript submission deadline
31 July 2023
Viewed by
1303

Topic Information

Dear Colleagues,

Mycobacterium tuberculosis is the major etiological agent for tuberculosis (TB), an infectious disease. TB is the leading cause of single pathogen infection-related deaths with more than 4000 TB-related deaths reported every day worldwide. In 2019, approximately 10 million individuals were diagnosed with TB and an estimated 25% of the population suffered from latent TB. The World Health Organization (WHO) has aimed to reduce TB-related deaths and infections by 90% and 80% by 2030, respectively, when compared with those reported in 2015. To achieve this goal, novel safe, and effective antibiotics must be developed against intracellular, non-replicant, and resistant strains. On the other hand Non-tuberculous mycobacteria (NTM) are ubiquitously present in the environment, but NTM diseases occur infrequently. NTM are generally considered to be less virulent than Mycobacterium tuberculosis, however, these organisms can cause diseases in both immunocompromised and immunocompetent hosts. Therefore, there is an urgent need to develop novel drugs for effectively treating MDR-TB, and NTM decreasing the treatment duration, and minimizing the toxicity and cost of the drugs. This Research Topic requires the coordinated effort of multiple scientific disciplines as microbiology, pharmacology, chemistry, medical and correlated. We welcome your contributions on all aspects of novel drugs for treating MDR-TB in this Topic.

Prof. Dr. Fernando Rogério Pavan
Prof. Dr. Alzir Azevedo Batista
Dr. Adelino Vieira de Godoy Netto
Dr. Daniela Fernandes Ramos
Topic Editors

Keywords

  • mycobacterium tuberculosis
  • nontuberculous mycobacteria
  • new drugs

Participating Journals

Journal Name Impact Factor CiteScore Launched Year First Decision (median) APC
Biomedicines
biomedicines
4.757 3.0 2013 17.4 Days 2200 CHF Submit
Future Pharmacology
futurepharmacol
- - 2021 19.7 Days 1000 CHF Submit
Journal of Clinical Medicine
jcm
4.964 4.4 2012 18 Days 2600 CHF Submit
Pharmaceutics
pharmaceutics
6.525 6.0 2009 15.9 Days 2600 CHF Submit
Tropical Medicine and Infectious Disease
tropicalmed
3.711 4.8 2016 15.1 Days 2000 CHF Submit

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Published Papers (1 paper)

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Article
Latent Tuberculosis: A Promising New Compound to Treat Non-Replicating and Intramacrophagic Mycobacteria
Biomedicines 2022, 10(10), 2398; https://doi.org/10.3390/biomedicines10102398 - 26 Sep 2022
Cited by 1 | Viewed by 755
Abstract
As a biologic reservoir of Mycobacterium tuberculosis (M. tb), one-quarter of the world population is infected with the well-known latent tuberculosis (LTBI). About 5–10% of LTBI patients will progress to active disease in the first years after primary infection and, despite [...] Read more.
As a biologic reservoir of Mycobacterium tuberculosis (M. tb), one-quarter of the world population is infected with the well-known latent tuberculosis (LTBI). About 5–10% of LTBI patients will progress to active disease in the first years after primary infection and, despite using the recommended treatment, 20% can still reactivate the infection. A new LTBI treatment could minimize adverse effects and antibiotic resistance that can occur when the same drug is used to treat the latent and active disease. New hydrazones were evaluated, and they showed great inhibitory activity against intramacrophagic and non-replicating M. tb, commonly found at this stage of infection, in addition to bactericidal and narrow-spectrum activity. When tested against eukaryotic cells, the hydrazones showed great safety at different exposure times. In vitro, these compounds performed better than isoniazid and could be considered new candidates for LTBI treatment, which may promote greater engagement in its prescription and adherence. Full article
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