Synthetic protein conjugate vaccines provide protection against Mycobacterium tuberculosis in mice.
Cameron C HannaAnneliese S AshhurstDiana QuanJoshua W C MaxwellWarwick J BrittonRichard J PaynePublished in: Proceedings of the National Academy of Sciences of the United States of America (2021)
The global incidence of tuberculosis remains unacceptably high, with new preventative strategies needed to reduce the burden of disease. We describe here a method for the generation of synthetic self-adjuvanted protein vaccines and demonstrate application in vaccination against Mycobacterium tuberculosis Two vaccine constructs were designed, consisting of full-length ESAT6 protein fused to the TLR2-targeting adjuvants Pam2Cys-SK4 or Pam3Cys-SK4 These were produced by chemical synthesis using a peptide ligation strategy. The synthetic self-adjuvanting vaccines generated powerful local CD4+ T cell responses against ESAT6 and provided significant protection in the lungs from virulent M. tuberculosis aerosol challenge when administered to the pulmonary mucosa of mice. The flexible synthetic platform we describe, which allows incorporation of adjuvants to multiantigenic vaccines, represents a general approach that can be applied to rapidly assess vaccination strategies in preclinical models for a range of diseases, including against novel pandemic pathogens such as SARS-CoV-2.
Keyphrases
- mycobacterium tuberculosis
- sars cov
- pulmonary tuberculosis
- protein protein
- cancer therapy
- pulmonary hypertension
- amino acid
- high fat diet induced
- binding protein
- inflammatory response
- immune response
- risk factors
- emergency department
- high throughput
- adipose tissue
- bone marrow
- toll like receptor
- adverse drug
- hepatitis c virus
- wild type
- antiretroviral therapy