Tuberculosis (TB), caused by the intracellular pathogen Mycobacterium tuberculosis ( Mtb ), affects the lungs of infected individuals (pulmonary TB) but can also affect other sites (extrapulmonary TB). The only licensed vaccine Mycobacterium bovis bacillus Calmette-Guerin (BCG) protects infants and young children but exhibits variable efficacy in protecting against adult pulmonary TB. Poor compliance and prolonged treatment regimens associated with the use of chemotherapy has contributed to the development of multidrug-resistant (MDR) and extensively drug-resistant (XDR) Mtb . Thus, there is an urgent need for the design of more effective vaccines against TB. The development of safe and novel adjuvants for human use is critical. In this study, we demonstrate that saponin-based TQL1055 adjuvant when formulated with a TLR4 agonist (PHAD) and Mtb specific immunodominant antigens (ESAT-6 and Ag85B) and delivered intramuscularly in mice, the SA-TB vaccine induced potent lung immune responses. Additionally, the SA-TB vaccine conferred significant protection against Mtb infection, comparable with levels induced by BCG. These findings support the development of a SA-TB vaccine comprising TQL1055, as a novel, safe and effective TB vaccine for potential use in humans.
Keyphrases
- mycobacterium tuberculosis
- multidrug resistant
- drug resistant
- pulmonary tuberculosis
- immune response
- acinetobacter baumannii
- endothelial cells
- emergency department
- gram negative
- early stage
- pulmonary hypertension
- toll like receptor
- dendritic cells
- climate change
- radiation therapy
- inflammatory response
- metabolic syndrome
- cystic fibrosis
- type diabetes
- oxidative stress
- klebsiella pneumoniae
- hepatitis c virus
- adipose tissue
- high fat diet induced
- high glucose
- combination therapy
- diabetic rats
- bacillus subtilis
- stress induced
- anti inflammatory
- human health