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. 2008 Jul 30;82(20):10032–10041. doi: 10.1128/JVI.01050-08

TABLE 1.

N36Mut(e,g) and neutralizing gp41-directed MAbs inhibit infectivity synergistically in an HBX2 Env-pseudotyped virus neutralization assaya

Ab peptide Ab/N36Mut(e,g) combination ratio DRI (mean ± SD)
CI (mean ± SD)
Ab N36Mut(e,g)
bF-3674b 1:20 2.4 ± 0.6 7.4 ± 1.6 0.6 ± 0.2
1:40 4.0 ± 0.9 6.4 ± 1.2 0.4 ± 0.2
1:80 7.0 ± 1.5 5.6 ± 0.9 0.3 ± 0.1
1:100 10.0 ± 2.7 6.4 ± 1.5 0.3 ± 0.1
1:200 10.4 ± 2.3 3.3 ± 0.6 0.4 ± 0.1
mF-3674b 1:10 3.7 ± 1.0 3.5 ± 0.8 0.6 ± 0.2
1:20 11.8 ± 2.4 5.5 ± 0.9 0.3 ± 0.1
2F5 1:500 3.4 ± 1.0 8.4 ± 1.6 0.4 ± 0.2
1:1,000 8.2 ± 1.9 9.7 ± 1.2 0.2 ± 0.1
4E10 1:500 6.2 ± 1.5 12.7 ± 2.7 0.3 ± 0.1
1:1,000 12.0 ± 2.6 12.1 ± 2.2 0.2 ± 0.1
a

The IC50s of the antibodies alone are as follows: bF-3674, 88 ± 14 nM; mf-3674, 603 ± 91 nM; 2F5, 3.8 ± 1.0 nM; 4E10, 6.3 ± 3.7 nM. The IC50 for N36Mut(e,g) is 5.7 ± 0.5 μM.

b

bF-3674 and mF-3674 are the bivalent and monovalent versions of Fab 3674, respectively (16).