MIP3α-Rel<sub>Mtb</sub> intranasal DNA vaccination induces reactive T-cell infiltration into the lungs of mice and macaques.
Ontology highlight
ABSTRACT: Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis (TB), is the leading cause of mortality due to a single infectious organism. While generally curable, TB requires a lengthy and complex antibiotic regimen, due in large part to persistent bacteria that survive antibiotic exposure. RelMtb is the primary enzyme regulating the stringent response, which contributes to Mtb persistence. Targeting RelMtb with a vaccine to eliminate persistent bacteria in combination with antibiotics to kill dividing bacteria has shown promise in model systems. In a mouse model of Mtb infection, a vaccine created by genetically fusing relMtb to the chemokine macrophage inflammatory protein 3α (MIP3α), a ligand for the CC chemokine receptor type 6 (CCR6) present o
SUBMITTER: Gordy JT
PROVIDER: S-EPMC12313244 | biostudies-literature | 2025 Aug
REPOSITORIES: biostudies-literature
ACCESS DATA