Autor: |
Nguyen, Michelle, Ahn, Phillip, Dawi, John, Gargaloyan, Areg, Kiriaki, Anthony, Shou, Tiffany, Wu, Kevin, Yazdan, Kian, Venketaraman, Vishwanath |
Předmět: |
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Zdroj: |
Clinics & Practice; Feb2024, Vol. 14 Issue 1, p198-213, 16p |
Abstrakt: |
Tuberculosis (TB), a respiratory disease caused by Mycobacterium tuberculosis (Mtb), is a significant cause of mortality worldwide. The lung, a breeding ground for Mtb, was once thought to be a sterile environment, but has now been found to host its own profile of microbes. These microbes are critical in the development of the host immune system and can produce metabolites that aid in host defense against various pathogens. Mtb infection as well as antibiotics can shift the microbial profile, causing dysbiosis and dampening the host immune response. Additionally, increasing cases of drug resistant TB have impacted the success rates of the traditional therapies of isoniazid, rifampin, pyrazinamide, and ethambutol. Recent years have produced tremendous research into the human microbiome and its role in contributing to or attenuating disease processes. Potential treatments aimed at altering the gut-lung bacterial axis may offer promising results against drug resistant TB and help mitigate the effects of TB. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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