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Hum Vaccin Immunother 2015[Aug]; 11 (8): 1954-60 PMID26091147show ga
Tuberculosis (TB) still remains a major public health issue despite the current available vaccine for TB, Bacille Calmette Guerin (BCG). An effective vaccine against TB remains a top priority in the fight against this pandemic bacterial infection. Adequate protection against TB is associated with the development of TH1-type and CD8+ T cell responses. One alarmin cytokine, interleukin 33 (IL-33), has now been implicated in the development of both CD4+ TH1 and CD8+ T cell immunity. In this study, we determined whether the administration of IL-33 as an adjuvant, encoded in a DNA plasmid, could enhance the immunogenicity of a TB DNA vaccine. We report that the co-immunization of IL-33 with a DNA vaccine expressing the Mycobacterium Tuberculosis (Mtb) antigen 85B (Ag85B) induced robust Ag85B-specific IFN? responses by ELISpot compared to Ag85B alone. Furthermore, these enhanced responses were characterized by higher frequencies of Ag85B-specific, multifunctional CD4+ and CD8+ T cells. Vaccination with IL-33 also increased the ability of the Ag85B-specific CD8+ T cells to undergo degranulation and to secrete IFN? and TNF? cytokines. These finding highlights IL-33 as a promising adjuvant to significantly improve the immunogenicity of TB DNA vaccines and support further study of this effective vaccine strategy against TB.
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Hum+Vaccin+Immunother 2015 ; 11 (8): 1954-60
