Table 4.

Inhibition of HIV-1 fusion by either STAg or C-18 is not mediated by production of the β-chemokines MIP-1α and MIP-1β


Inhibitor (dose, μg/mL)

Antibodies (μg/mL)

No. of syncytia (% inhibition) PM1/12E1(JR-FL Env)
None None 305 ± 24 
STAg (10)   —   121 ± 10 (60)  
 αMIP-1α/MIP-1β (2) 124 ± 2 (59) 
C-18 (10)   —   72 ± 10 (76)  
 αMIP-1α/MIP-1β (2) 71 ± 12 (77) 
MIP-1α + MIP-1β   —   53 ± 4 (83)  

 
αMIP-1α/MIP-1β (2)
 
280 ± 32 (8)
 

Inhibitor (dose, μg/mL)

Antibodies (μg/mL)

No. of syncytia (% inhibition) PM1/12E1(JR-FL Env)
None None 305 ± 24 
STAg (10)   —   121 ± 10 (60)  
 αMIP-1α/MIP-1β (2) 124 ± 2 (59) 
C-18 (10)   —   72 ± 10 (76)  
 αMIP-1α/MIP-1β (2) 71 ± 12 (77) 
MIP-1α + MIP-1β   —   53 ± 4 (83)  

 
αMIP-1α/MIP-1β (2)
 
280 ± 32 (8)
 

— indicates no antibody added.

MIP-1α and MIP-1β (Peprotech). STAg, or C-18 was added to PM1 cells alone or in the presence of αMIP-α/MIP-1β antibodies for 60 minutes at 37°C at the indicated concentrations. Then, 12E1 effector cells (infected overnight with vCB28) were added, and fusion was recorded after 3 to 4 hours.

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