Enhancement of immune response against Mycobacterium tuberculosis HspX antigen by incorporation of combined molecular adjuvant (CASAC)

•CASAC improves humoral immunity against HspX antigen with secretion of antigen-specific IgG1 and IgG2a antibody.•CASAC is a good adjuvant to induce Th1-mediated memory CD8+ T-cell response against HspX antigen.•Combination of HspX antigen and CASAC is effective to induce strong humoral and cellular...

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Veröffentlicht in:Molecular immunology 2020-01, Vol.117, p.54-64
Hauptverfasser: Lew, Min Han, Norazmi, Mohd Nor, Tye, Gee Jun
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Sprache:eng
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Zusammenfassung:•CASAC improves humoral immunity against HspX antigen with secretion of antigen-specific IgG1 and IgG2a antibody.•CASAC is a good adjuvant to induce Th1-mediated memory CD8+ T-cell response against HspX antigen.•Combination of HspX antigen and CASAC is effective to induce strong humoral and cellular immunity in C57BL/6 mouse model. Tuberculosis (TB) is one of the deadliest human diseases worldwide caused by mycobacterial infection in the lung. Bacillus Calmette-Guerin (BCG) vaccine protects against disseminated TB in children, but its effectiveness is still questionable due to highly variable protections in adolescence and elderly individuals. Targeting the latency M.tb antigen is a recent therapeutic approach to eradicate dormant pathogen that could possibly lead to disease activation. In this study, we aimed to potentiate immune responses elicited against 16 kDa α-crystalline (HspX) tuberculosis latency antigen by incorporation of Combined Adjuvant for Synergistic Activation of Cellular immunity (CASAC). Histidine-tagged recombinant HspX protein was initially produced in Escherichia coli and purified using Ni-NTA chromatography. To evaluate its adjuvanticity, C57BL/6 mice (n = 5) were initially primed and intradermally immunised in 2-weeks interval for 4 rounds with recombinant HspX, formulated with and without CASAC. Humoral and cell-mediated immune responses elicited against HspX antigen were evaluated using ELISA and Flow Cytometry. Our findings showed that CASAC improved humoral immunity with increased antigen-specific IgG1 and IgG2a antibody response. Stronger CD8+ and Th1-driven immunity was induced by CASAC formulation as supported by elevated level of IFN-γ, TNF-α, IL-12 and IL-17A; and with low IL-10 secretion. Interestingly, adjuvanted HspX vaccine triggered a higher percentage of effector memory T-cell population than those immunised with unadjuvanted vaccine. In conclusion, CASAC adjuvant has great potential to enhance immunogenicity elicited against HspX antigen, which could be an alternative regimen to improve the efficacy of future therapeutic vaccine against Mycobacterium tuberculosis.
ISSN:0161-5890
1872-9142
DOI:10.1016/j.molimm.2019.10.023