Immune system power may lessen reliance on antibiotics for tuberculosis

By Elissa Wolfson, The Science Advisory Board assistant editor

March 24, 2023 -- Francis Crick Institute researchers have found that the body's natural process of removing old and damaged cell parts may be an essential part of tackling infections like tuberculosis (TB) that take hold within cells. They hypothesized that harnessing this process might present alternatives to antibiotics or improve antibiotic use. Their study was published in Nature Microbiology on Friday -- World TB Day.

TB is caused by bacteria (Mycobacterium tuberculosis) that most often affect the lungs. Untreated TB killed 1.6 million people in 2021. Although a long course of different antibiotic treatments is required to effectively remove the infection, TB is curable and preventable.

To combat infections like TB, the team studied genes key to bacteria's ability to evade autophagy, a pathway used by cells to destroy themselves when they are stressed or infected. They engineered human immune cells called macrophages from induced pluripotent stem cells, which have the ability to become any cell type in the body. They then used genome editing tools to manipulate the macrophages' ability to perform autophagy.

When genes key to autophagy were removed and the cells were infected with M. tuberculosis, the bacterial infection took hold, increasing replication within the engineered cells and causing mass host-cell death. The team validated their results using macrophages isolated from blood samples, confirming the importance of autophagy in human defenses.

The researchers believe that if autophagy's strong role in controlling intracellular infections like TB can be strengthened, it could provide new avenues for tackling antibiotic resistance. However, they note that boosting the autophagy pathway is complex, since all parts of the body use autophagy to recycle old and damaged cells. To safely increase autophagy where infections occur, researchers must target the pathway in macrophages alone. The team is now planning to screen for drug compounds that could boost autophagy in such a targeted way. Their goal is to make existing antibiotic drugs more effective, or present alternatives to antibiotic drugs in cases where bacteria have evolved resistance.

"Antibiotic resistance is a huge threat to our health so it's incredibly important to understand how our bodies fight infection and where there might be room for improvement," Beren Aylan, joint first author and a Crick PhD student, said in a statement. "Anything that can be done to more effectively remove bacteria could also make a huge difference to the cost and accessibility of treatments."

Study finds tuberculosis vaccines cost-effective in lower-income countries
Harvard University researchers and collaborators conducted a modeling study that showed tuberculosis vaccination could be cost-effective in 73 of 105...
Researchers learn why Huntington's disease turns on with age
Washington University School of Medicine researchers have discovered that when Huntington's disease patients age the fatal neurological disorder gradually...
Preclinical data on long-acting tuberculosis drug raises hopes for simplified treatment
A long-acting injectable formulation of rifabutin has delivered high plasma concentrations for 16 weeks in mice, resulting in the prevention of tuberculosis...
Researchers identify how bacterium that causes tuberculosis evolves rapidly
A new study has identified how the bacterium that causes tuberculosis can evolve rapidly in response to new environments, providing insights into how...
ZebiAI, TB Alliance collaborate on tuberculosis targets
Biotech firm ZebiAI has announced a collaboration agreement with nonprofit TB Alliance to further the discovery, development, and delivery of tuberculosis...
Thermally stable TB vaccine may now be possible thanks to an innovative new process
Researchers at the University of Bath have developed a process that protects vaccines from heat damage by trapping them in silica cages. The results were...

Copyright © 2023 scienceboard.net


Conferences
Connect
Science Advisory Board on LinkedIn
Science Advisory Board on Facebook
Science Advisory Board on Twitter