The immunogenicity and toxicity of a purified influenza vine (N2) neur
aminidase vaccine (NAV) were investigated in 88 human subjects aged 18
-40, and compared to response to a conventional trivalent influenza va
ccine, Fluogen (Parke-Davis). NAV doses ranged from 2.6 to 69.9 mu g a
nd were given intramuscularly. Serologic neuraminidase-inhibiting (NI)
and neuraminidase-specific ELISA responses in this N2-primed populati
on were roughly proportional to the dose administered Maximal response
was seen in 14-21 days and NI antibody titers persisted unabated for
the 6-month post-vaccination follow-lip period. All doses were well to
lerated with respect to local and systemic reactions. NI tests perform
ed with the putative (1975) priming N2 antigen demonstrated anamnestic
response but did not reveal responses not already shown with the homo
logous (1992) antigen. Response to this purified, non-adjuvanted prepa
ration encourages continuing investigation of the induction of infecti
on-permissive immunity with influenza virus neuraminidase.