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. 2011 Aug;85(16):8227–8240. doi: 10.1128/JVI.00767-11

Table 1.

Affinities and maximal binding of CCR5 MAbs to CD4+ T cells and U87-CD4-CCR5 cells

MAb Isotype Epitopea CD4+ T cellsb
U87-CD4-CCR5 cellsb
EC50 (μg/ml) Maximal GMFI EC50 (μg/ml) Maximal GMFI
PA8 IgG1 NT 22 ± 9.9 44 ± 4.0 12 ± 6.7 400 ± 37
PA11 IgG1 NT 9.8 ± 6.9 410 ± 47 34 ± 11 1,500 ± 177
45502 IgG2B NT 85 ± 19 36 ± 6.8 NA 0c
CTC5 IgG1 NT 3.6 ± 2.6 210 ± 20 19 ± 2.7 2,000 ± 80
PA10 IgG1 NT-ECL2d >200 >2,600 215 ± 138 380 ± 106
PA14 IgG1 NT-ECL2 9.1 ± 4.1 500 ± 36 10 ± 3.6 1,300 ± 78
2D7 IgG2A ECL2 1.5 ± 0.76 340 ± 22 1.2 ± 0.26 980 ± 26
45531 IgG2B ECL2 6.3 ± 1.0 490 ± 12 16 ± 6.2 1,400 ± 98
45523 IgG2B MD 31 ± 6.8 75 ± 3.6 139 ± 47 1,600 ± 209
45549 IgG2B MD NA 0c 40 ± 8.6 800 ± 67
a

As defined in references 29 and 40. MD, multidomain.

b

EC50 and GMFI values (±standard errors of the mean [SEM]) are based on the fitted curves generated from the data points shown in Fig. 1. EC50 is the MAb concentration giving half-maximal binding. Maximal GMFI is the fitted plateau value. Therefore, it might not always be the same as the highest value reached in Fig. 1. The data were derived from one experiment of two performed for each cell type. The purified CD4+ T cells expressed high levels of CD4 (GMFI = 5,000). NA, not applicable.

c

No binding detectable.

d

The PA10 epitope was originally reported to involve both the NT and ECL2 (40), but the MAb was later shown to bind to a tyrosine-sulfated NT peptide (12). Whether ECL2 residues are also involved is not clear.