Direct DNA inoculations are being developed as a method of subunit vac
cination. Plasmid DNAs encoding influenza virus hemagglutinin glycopro
teins have been tested for the ability to provide protection against l
ethal influenza challenges. In immunization trials using inoculations
of purified DNA in saline, 67-95% of test mice and 25-63% of test chic
kens were protected against the lethal challenge. Good protection was
achieved by intramuscular, intravenous and intradermal injections. In
mice, 95% protection was achieved by gene gun delivery of 250-2500 tim
es less DNA than the saline inoculations. Successful DNA vaccination b
y multiple routes of inoculation and the high efficiency of gene-gun d
elivery highlight the potential of this promising new approach to immu
nization.