Table 5.

Antibodies against MIP-1α, MIP-1β chemokines inhibit fusion enhancement of MDMs with X4 envelope-expressing cells when added to the IFN-γ/IL-6–treated MDMs

Treatment5-151Antibodies5-152No. of syncytia5-150
IIIBJR-FL
None None 9 ± 1 156 ± 1 
a-MIP-1α; a-MIP-1β a-MIP-1α; a-MIP-1β 8 ± 2 161 ± 20 
IFN-γ None 33 ± 3 37 ± 5 
IFN-γ a-MIP-1α; a-MIP-1β 5 ± 1 127 ± 17 
IL-6 None 32 ± 5 109 ± 9  
IL-6 a-MIP-1α; a-MIP-1β 2 ± 1 183 ± 6 
Treatment5-151Antibodies5-152No. of syncytia5-150
IIIBJR-FL
None None 9 ± 1 156 ± 1 
a-MIP-1α; a-MIP-1β a-MIP-1α; a-MIP-1β 8 ± 2 161 ± 20 
IFN-γ None 33 ± 3 37 ± 5 
IFN-γ a-MIP-1α; a-MIP-1β 5 ± 1 127 ± 17 
IL-6 None 32 ± 5 109 ± 9  
IL-6 a-MIP-1α; a-MIP-1β 2 ± 1 183 ± 6 

MIP indicates macrophage inflammatory protein; MDMs, monocyte-derived macrophages; IFN-γ, interferon γ; IL-6, interleukin 6.

F5-150

Syncytia were scored after 18 hours of coculture of the macrophages and the effector cells: TF228 cells expressing IIIB envelope or 12E1 cells infected with recombinant vaccinia virus expressing R5 envelope (vCB28, JR-FL). Data represent 2 experiments.

F5-151

MDMs were treated with cytokines for the last 24 hours of the culture.

F5-152

Anti–MIP-1α and anti–MIP-1β antibodies were used at 2 μg/mL. Antibodies were added to MDMs simultaneously with cytokines.

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