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. 2006 Sep;80(17):8745–8762. doi: 10.1128/JVI.00956-06

TABLE 4.

Epitope specificities of serum antibodies determined by MAb binding competition

Group Binding to JRFL gp120a Neutralization of JRFLb
Competition titerc
CD4BS
Glycan (2G12) V3
CD4i (X5/sCD4) Cluster I (7B2)
Standard After CD4 b6 15e b12 LE311 LE311/sCD4
SF162gp140 5,000 <100 6,000 <100 <100 <100 <100 125 250 <100 <100
ΔV2gp140 4,000 <100 3,000 100 225 <100 <100 100 500 <100 <100
ΔV3gp140 10,000 <100 120 <100 100 <100 <100 100 500 150 <100
ΔV2ΔV3gp140 17,000 <100 <100 100 125 <100 <100 <100 150 <100 <100
SHIVSF162P4d 150,000 250 >30,000 300,000 500 <100 500 17,000 70,000 24,000 >25,000
Prebleede <1,000 <100 <100 <100 <100 <100 <100 <100 <100 <100 <100
Selff 0.01 0.08 0.02 0.2 0.008 0.008 0.005 0.005
a

Values indicate the reciprocal serum dilution resulting in half-maximal binding.

b

Values indicate reciprocal serum dilution resulting in 50% neutralization in the absence of sCD4 (standard) or following preincubation of viruses with sCD4 (after CD4).

c

Values indicate the reciprocal serum dilution at which MAb-mediated virus capture was competed 50%.

d

For SHIVSF162P4, the sera tested were collected 643 days postinfection.

e

For prebleed, preimmunization sera pooled from all animals were included in all groups.

f

Self denotes competition with the same MAb used for capture recorded in μg/ml.