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. 2002 Jul;76(14):6882–6892. doi: 10.1128/JVI.76.14.6882-6892.2002

TABLE 1.

Immunogens used and their FIV contentsa

Immunogen Composition Mean % IF-positive cells ± SDb Mean virus content/106 cells ± SD
Infectivity
Proteinc (μg) RNAd (no. of copies) In vitroe In vivof
FCPLB Infected, fixed PLB 54 ± 1 50 ± 2 (5.0 ± 0.6) × 109
ID-1 PLB + AT2-FIV 23 ± 2 15 ± 1 (5.8 ± 0.8) × 108
ID-2 PLB + AT2-FIV + peptide SU5 20 ± 3 11 ± 1 (2.6 ± 0.5) × 108
ID-3 PLB + AT2-FIV + peptide TM59 24 ± 1 12 ± 2 (2.4 ± 0.3) × 108
Mock-1 PLB 0 0 <103
Mock-2 PLB + peptides SU5 and TM59 0 0 <103
a

Values shown are the means ± the standard deviations of the immunogens prepared for each prospective vaccinee.

b

That is, the percent membrane IF-positive cells when probed with anti-FIV serum and anti-cat IgG polyclonal serum conjugated with fluorescein isothiocyanate.

c

Cells were lysed in sodium dodecyl sulfate-electrophoresis sample buffer at 60°C for 30 min, electrophoresed, and examined by using a semiquantitative Western blot assay.

d

Cells were lysed and tested for viral RNA by TM-PCR.

e

Cells were tested for FIV infectivity by inoculation into MBM cells, which were then monitored for FIV production for 8 weeks.

f

Based on testing immunized cats by virus isolation and TM-PCR 5.5 months after the first inoculation of the immunogens.