A low-cost drug, nitazoxanide, could curb M. tuberculosis by harnessing cells' RNA sensors. Courtesy of NIAID
Current treatment regimens for Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis, are long, complex, and hard for people to sustain. Moreover, the bacteria often develop drug resistance, and many people harbor multi-drug-resistant strains. In 2018 alone, nearly 1.5 million people died from tuberculosis worldwide.
Now, a study in Science suggests a new approach that might help: making people's cells better at killing Mtb by harnessing RNA sensors in our cells, which detect the RNA of invading pathogens.
RNA sensing is part of our first-line immune defense. For the first time, researchers led by Anne Goldfeld, MD, of Boston Children's Hospital's Program in Cellular and Molecular Medicine, showed that RNA sensing is important in inhibiting Mtb's growth once it gets inside cells.
By studying infected cells, the team showed that Mtb activates several major RNA sensors -- RIG-I, MDA5, PKR, and MAVS -- that in turn inhibit bacterial growth. When they disrupted any of these sensors using gene-editing methods such as CRISPR, Mtb grew to significantly higher levels in human cells.
"This was a key breakthrough, because RNA sensor molecules were previously thought to be involved in fighting viruses and not bacteria," Goldfeld says. "It suggested that enhancing the activity of these RNA sensors via drug therapy could curb MTb growth."
Recently, Goldfeld's lab, together with the lab of her colleague Sun Hur, PhD, showed that an FDA-approved antiparasitic drug called nitazoxanide (NTZ) inhibits the Ebola virus, and that it works by amplifying RNA sensor activities. That finding, coupled with the new discovery that RNA sensors inhibit Mtb growth within cells, led Goldfield's team to try NTZ in tuberculosis.
"We showed that NTZ amplifies the activities of RNA sensors once they have been triggered by Mtb RNA," Goldfeld says. "And unexpectedly, we found that NTZ also amplifies MTB's stimulation of RNA sensor activity."
The net result was that NTZ increased production of interferon and IFITM3, important elements of the immune response against tuberculosis, and significantly inhibited Mtb growth inside cells. Although more research is needed to better understand how NTZ does all this, Goldfeld hopes these studies will open a new approach to alleviate the global burden of tuberculosis.
"NTZ is low in cost and available as an oral drug, including a syrup formulation for children, making it an easily accessible treatment," she says. "We think NTZ or a derivative drug could complement traditional tuberculosis regimens by boosting host defenses to kill Mtb. The power of this approach is that targeting host factors will not precipitate or increase antibiotic resistance in bacteria."
Shahin Ranjbar and Viraga Haridas of the Program in Cellular and Molecular Medicine (PCMM) were co-first authors on the paper. Coauthors were Aya Nambu, Luke Jasenosky, Supriya Sadhukhan, and James Falvo of PCMM; Thomas Ebert and Veit Hornung of Ludwig-Maximilians-Universität München (Munich, Germany); and Gail H. Cassell of Harvard Medical School.
This work was supported by the National Institutes of Health (AI125075), the Annenberg Foundation, the Ragon Institute, Romark Inc., John Moores, Jeanne Sullivan, the Campbell Foundation, and a lab gift from Romark, Inc., which makes NTZ.