Journal Article Review Ppublish 4 citations
PubMed: 39360834 DOI: 10.1128/cmr.00080-23
Toward better cures for Mycobacterium abscessus lung disease.
Clin Microbiol Rev 37(4):e0008023
Authors: Véronique Dartois, Thomas Dick
Affiliations
- Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, New Jersey, USA.
- Department of Medical Sciences, Hackensack Meridian School of Medicine, Nutley, New Jersey, USA.
- Department of Microbiology and Immunology, Georgetown University, Washington, DC, USA.
Abstract
SUMMARYThe opportunistic pathogen Mycobacterium abscessus (Mab) causes fatal lung infections that bear similarities-and notable differences-with tuberculosis (TB) pulmonary disease. In contrast to TB, no antibiotic is formally approved to treat Mab disease, there is no reliable cure, and the discovery and development pipeline is incredibly thin. Here, we discuss the factors behind the unsatisfactory cure rates of Mab disease, namely intrinsic resistance and persistence of the pathogen, and the use of underperforming, often parenteral and toxic, repurposed drugs. We propose preclinical strategies to build injectable-free sterilizing and safe regimens: (i) prioritize oral bactericidal antibiotic classes, with an initial focus on approved agents or advanced clinical candidates to provide immediate options for desperate patients, (ii) test drug combinations early, (iii) optimize novel leads specifically for M. abscessus, and (iv) consider pharmacokinetic-pharmacodynamic targets at the site of disease, the lung lesions in which drug tolerant bacterial populations reside. Knowledge and tool gaps in the preclinical drug discovery process are identified, including validated mouse models and computational platforms to enable in vitro mouse-human translation. We briefly discuss recent advances in clinical development, the need for readouts and biomarkers that correlate with cure, and clinical trial concepts adapted to the uniqueness of Mab patient populations for new regimen development. In an era when most pharmaceutical firms have withdrawn from antimicrobial drug discovery, the breakthroughs needed to fill the regimen development pipeline will likely come from partnerships between academia, biotech, pharma, non-profit organizations, and governments, with incentives that reward cooperation.
MeSH
Drug Discovery, Lung, Mycobacterium, Pharmaceutical Preparations, Mycobacterium Abscessus, Microbiology, Lung Diseases, Communicable Diseases
Cited by
- Toward a Bactericidal Oral Drug Combination for the Treatment of Mycobacterium abscessus Lung Disease. ACS Infect Dis, 2025
- A Year in Review on Tuberculosis and Non-tuberculous Mycobacteria Disease: A 2025 Update for Clinicians and Scientists. Pathog Immun, 2025
- Activity of combinations of bactericidal and bacteriostatic compounds in Mycobacterium abscessus-infected mice: an overview. Front Microbiol, 2025
- Next-generation rifamycins for the treatment of mycobacterial infections. Proc Natl Acad Sci U S A, 2025