Cm. Leutenegger et al., PARTIAL PROTECTION BY VACCINATION WITH RECOMBINANT FELINE IMMUNODEFICIENCY VIRUS SURFACE GLYCOPROTEINS, AIDS research and human retroviruses, 14(3), 1998, pp. 275-283
In an effort to induce a strong immune response that might protect aga
inst feline immunodeficiency virus (FIV) challenge infection, three gr
oups of five specified pathogen-free (spf) cats each were immunized su
bcutaneously with different FIV antigen preparations, Immunizations we
re done at weeks 0, 2, and 4 with 100 mu g of recombinant SU from an F
IV Zurich 2 (FIV Z2) strain expressed by E. coli (group 1) or the bacu
lovirus expression system (groups 2 and 3) adsorbed on aluminum hydrox
yde and administered with QS-21 (groups 1 and 2) or Freund's adjuvant
together with the recombinant nucleocapsid protein (protein NC) of rab
ies virus (group 3), Protein NC was described to act as an exogenous s
uperantigen. Group 3 cats demonstrated the highest detectable antibody
response to the vaccine antigen as determined by ELISA and Western bl
ot analysis, All immunized cats together with seven control animals we
re challenged with 20 CID50 of cat lymphocyte-grown FIV Z2 3 weeks fol
lowing the last immunization, Whereas virus was readily recovered from
peripheral blood lymphocytes of seven of seven nonvaccinated control
cats following this challenge dose, virus was not recovered from two c
ats of groups 1 and 2, All cats in groups 2 and 3 showed a provirus lo
ad significantly decreased to 3% of that of controls up to week 8 afte
r challenge infection, Eleven of 15 vaccinated cats and 5 of 7 control
cats developed virus-neutralizing antibodies by week 8 after challeng
e infection, The two cats negative on virus isolation remained seroneg
ative, developed no detectable virus-neutralizing activities, but were
repeatedly positive in provirus PCR, Moreover, starting at week 1 aft
er challenge, both cats showed the lowest provirus load in their respe
ctive groups, These results indicate that immunization with recombinan
t FIV SU in conjunction with appropriate adjuvants may lead to partial
protection against FIV challenge infection.