Two related DNA vaccine vector plasmids, harbouring either wild-type (pcDNA
3/ntetC) or synthetic codon optimised (pcDNA3/stetC) DNA encoding fragment
C (TetC) of tetanus toxin were constructed. COS-7 cells transformed with pc
DNA3/ stetC reproducibly expressed higher levels of TetC than similar cells
transformed with pcDNA3/ntetC. BALB/c mice immunised intramuscularly with
pcDNA3/stetC produced significantly higher levels of anti-TetC antibodies i
n their serum in the weeks following vaccination compared to mice immunised
with pcDNA3/ntetC, even when differences in the CpG content between the tw
o sequences were controlled for using non-expressing DNA. (C) 2000 Elsevier
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