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. 1998 Dec;72(12):9656–9667. doi: 10.1128/jvi.72.12.9656-9667.1998

TABLE 1.

Efficient removal of HIV-1 envelope-binding Abs from purified Ig from HIV-infected patients

Samplea ELISA endpoint antibody titer against:
ogp140451 gp120451 V3MN gp41582 p24
US20
 Purified Ig 409,600 51,200 12,800 6,400 204,800
 gp120-depleted fraction 204,800 (2b) 400 (128) 3,200 (4) 6,400 (1) 204,800
 ogp140-depleted fraction 1,600 (256) 400 (128) 1,600 (8) <400 (>16) 204,800
 gp120 Abs 25,600 12,800 400 <100 <100
 ogp140 Abs 51,200 12,800 400 400 800
HIVIG
 Purified Ig 1,638,400 409,600 25,600 102,400 1,600,000
 gp120-depleted fraction 819,200 (2) 200 (2,048) 3,200 (8) 102,400 (1) 1,600,000
 ogp140-depleted fraction 200 (8,192) 400 (1,024) 6,400 (4) 12,800 (8) 1,600,000
 V3MN-depleted fraction 819,200 (2) 409,600 (1) <100 (>256) NDc 1,600,000
 gp120 Abs 102,400 102,400 3,200 <800 1,600
 ogp140 Abs 409,600 102,400 3,200 25,600 3,200
a

Purified Ig, purified Ig from HIV-1 serum; gp120-, ogp140-, and V3MN-depleted fractions, HIV-1 sera depleted over gp120, ogp140, and V3MN columns, respectively; gp120 Abs and ogp140 Abs, Abs purified from HIV-1 serum by using gp120 and ogp140 affinity columns, respectively. Values for depleted fractions were normalized to the unfractionated Ig by correcting for the amount of Ab to p24, and affinity-purified (eluted) Abs were concentrated to the original volume of the Ig applied to each column, as described in Materials and Methods. 

b

Fold reduction compared to Ig. 

c

ND, not determined.