Table 2 |
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|
Neutralization titer against HIV-1 clinical isolates in BALB/c mice |
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|
Vaccine groups |
Neutralization titer against HIV-1 isolates |
|||||
|
XJDC6371 |
XJDC6431 |
XJDC0793 |
CBJB105 |
CBJB248 |
020101300 |
|
|
|
||||||
|
SV145 |
< 6 |
< 6 |
< 6 |
< 6 |
< 6 |
> 12 |
|
SV145-10M |
> 12 |
> 24 |
> 24 |
> 24 |
> 24 |
> 12 |
|
SV145M1&2 |
< 6 |
> 24 |
> 24 |
> 24 |
> 24 |
> 24 |
|
SV145M1 |
< 6 |
> 24 |
> 24 |
> 24 |
> 24 |
> 24 |
|
SV145M2 |
< 6 |
> 12 |
> 12 |
> 12 |
> 12 |
> 12 |
|
SV145M3 |
< 6 |
< 6 |
< 6 |
< 6 |
> 12 |
> 12 |
|
SV145M4 |
< 6 |
< 6 |
< 6 |
< 6 |
> 12 |
> 12 |
|
SV145M5 |
< 6 |
< 6 |
< 6 |
< 6 |
< 6 |
< 6 |
|
|
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|
The neutralization was conducted by using a panel of clinical isolates in PBMCs with 50% inhibitory dose. Gp145-10 M, gp145M1&2, gp145M1 and 145M2 groups could neutralize HIV-1 isolates at the highest titer of 1:24, other than XJDC6371. The single N-glycosylation site deletion in the V1 loop designated as gp145M2 could induce broader neutralizing antibodies against five clinical isolates at a titer of 1:12. |
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|
Liu et al. Retrovirology 2010 7:71 doi:10.1186/1742-4690-7-71 |
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