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. 1999 Apr;73(4):3292–3300. doi: 10.1128/jvi.73.4.3292-3300.1999

TABLE 3.

Postchallenge virological follow-up to determine whether sterilizing immunity was achieved

Group Animal Results obtained by PCR and QVI at wka:
Infection statusc postchallenge
2
4
6
12b
PCR QVI PCR QVI PCR QVI
gp120/DNA I038 + 27 + 3 + 3 + Infected
Q062 + 0 + 81 + 9 + Infected
I044 + 9 + 9 + 0 + Infected
X007 + 0.5 + 27 + 0 + Infected
rgp120/MF59 I046 + 0 0 0 Transient infection
T118 + 0 0 0 Transient infection
J041 + 0 0 0 Transient infection
Z64 d 0 0 0 Transient infection
rgp120/ISCOM T122 0 0 0 Protected
L159 + 0 0 0 Transient
Q048 + 1 0 0 Transient infection
X009 0 0 0 Protected
DNA controls Q045 + 9 + 0.5 + 1 + Infected
Q054 + 27 + 27 + 3 + Infected
Subunit protein controls EP4 + 3 + 9 + 27 + Infected
WK2 + 81 + 9 + 1 + Infected
a

Postchallenge virology was based on PCR of DNA from PBMC, with the results being scored as positive (+) or negative (−), and quantitative virus isolation (QVI), with values being the number of virus-producing cells per 106 PBMC. All PCR results were negative and all QVI values were 0 at week 0. 

b

Shown are PCR results for antibodies other than gp120. 

c

Protected, negative for virus by all parameters, including multiple nested PCR analysis of DNA from lymph node biopsy specimens; transient infection, positive at only one time point (week 2), by only one assay, and negative for virus by all parameters at all time points thereafter. 

d

Positive plasma RNA signal detected only at week 2 (see Fig. 3).