2,074
Views
0
CrossRef citations to date
0
Altmetric
Novel Vaccines

Saponin TQL1055 adjuvant-containing vaccine confers protection upon Mycobacterium tuberculosis challenge in mice

, , , , , & show all
Article: 2302070 | Received 14 Sep 2023, Accepted 02 Jan 2024, Published online: 08 Jan 2024
 

ABSTRACT

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.

Acknowledgments

This work was supported by Subcontract from Adjuvance Technologies, Inc HHSN272201700066C and Washington University in St. Louis, Department of Molecular Microbiology. The authors thank Lan Lu, Darya Urusova and Yun Tao for technical assistance. The authors have no conflicts to report

Disclosure statement

No potential conflict of interest was reported by the author(s).

Supplementary material

Supplemental data for this article can be accessed on the publisher’s website at https://doi.org/10.1080/21645515.2024.2302070

Additional information

Funding

The work was supported by the National Institute of Allergy and Infectious Diseases [HHSN272201700066C].