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Mycobacterium bovis BCG-vaccination in the guinea pig model of tuberculosis (TB) is sufficiently protective that candidate TB vaccines are judged against this. Little is understood about how the BCG vaccine works and, in the absence of a definitive correlate of protection, it is difficult to interpret the significance of novel vaccine induced host responses. Here an extended custom-made microarray (86 guinea pig genes) was used to dissect temporal changes in BCG-vaccine induced gene signatures to different mycobacterial antigens. Initially at 4h, pro-inflammatory genes such as IL-1α, IL-1β, IL-8 and GRO were up-regulated (P<0.001) and these were then superseded by IFN-γ and GM-CSF (at 12 and 20h) post-stimulation, ex vivo with PPD. Similar genes were seen following stimulation with viable BCG but with the addition of IL-23 (P<0.01) after 8h. Our results suggest that temporal changes in the up- and down-regulation of a variety of genes are required to trigger a successful protective response to TB in guinea pigs. This provides base-line information against which new TB vaccines can be compared.

More information Original publication

DOI

10.1016/j.vaccine.2010.09.061

Type

Journal article

Publication Date

2010-11-23T00:00:00+00:00

Volume

28

Pages

7979 - 7986

Total pages

7

Keywords

Animals, Antigens, Bacterial, BCG Vaccine, Cells, Cultured, Cytokines, Gene Expression Profiling, Gene Expression Regulation, Guinea Pigs, Oligonucleotide Array Sequence Analysis, Spleen, Time Factors, Tuberculosis, Up-Regulation