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. Author manuscript; available in PMC: 2013 Jan 14.
Published in final edited form as: J Immunol. 2010 Sep 8;185(7):4496–4505. doi: 10.4049/jimmunol.1001980

Table II.

Anti–GBV-C E2 Abs neutralize diverse HIV isolates

Ab Description Ab Identification HIV Isolate Number (see Table I for characteristics)
1 2 3 4 5 6 7 8 9 10 11
Human anti-E2 polyclonal IgG I-P1 8.1a 3.4 2.9 1.6 2.2 2.3 4.1 3.5 2.8 3.7 5.1
I-P2 2.6 8.3
I-P3 5.8 1.7 <10 <10
Rabbit anti-E2 protein polyclonal IgG R1b,c 4.3 5.0
R2 1.5 2.1 1.1 3.1 1.6 <10 <10 <10 <10 1.5 1.2
R3 9.3 10
R4 5.6 4.9 <10 <10 <10 <10 <10 2.1 1.7
Rabbit anti-E2 peptide polyclonal IgG rPep-1c >50 >50 >50 >50 >50 >50 >50
rPep-2 >50 >50 >50 >50
Mouse anti-E2 monoclonal IgG M1 (VS) 1.4 2.5 <5 <5 <5 <5 <5 <5 <5
M5 <5 <5
M6 1.8 1.1
Human anti-HIV monoclonal IgG 2F5 1.7
4E10 1.3
2G12 >5 0.2

IC50 results >5 μg/ml for mAbs or >30 μg/ml for polyclonal Abs are in bold.

a

Neutralization assays were performed in PBMCs for R5 isolates and MT-2 cells for X4 isolates.

b

Concentration (micrograms per milliliter) required to reduce HIV infectivity by 50% compared with control Ab (IC50).

c

Rabbits were immunized with either rGBV-C E2 protein (anti-E2) or the 17-aa peptide Ag recognized by the M6 murine mAb (anti-rPep) as described in Materials and Methods. Blank, not tested. The highest or lowest concentration tested is equal to or more than or less than, respectively.