Table 1.

Effect of MoAbs to Various Chemokine Receptors on Migratory Capacity of Monocyte-Derived DCs

Chemoattractant Treatment WithNo. of Migrated Cells
Mean ± SD
None None  7 ± 2  
RANTES  None  111 ± 10 
 Cont. IgG  114 ± 5  
 αCCR-1 MoAb  42 ± 4 
 αCCR-3 MoAb  45 ± 7  
 αCCR-5 MoAb 81 ± 7  
 αCXCR-4 MoAb  108 ± 5  
 αCCR-1 MoAb/αCCR-3 MoAb  24 ± 4  
 αCCR-1 MoAb/αCCR-5 MoAb 35 ± 4  
 αCCR-3 MoAb/αCCR-5 MoAb  33 ± 3 
 αCCR-1 MoAb/αCCR-3 MoAb/αCCR5 MoAb  19 ± 3 
Chemoattractant Treatment WithNo. of Migrated Cells
Mean ± SD
None None  7 ± 2  
RANTES  None  111 ± 10 
 Cont. IgG  114 ± 5  
 αCCR-1 MoAb  42 ± 4 
 αCCR-3 MoAb  45 ± 7  
 αCCR-5 MoAb 81 ± 7  
 αCXCR-4 MoAb  108 ± 5  
 αCCR-1 MoAb/αCCR-3 MoAb  24 ± 4  
 αCCR-1 MoAb/αCCR-5 MoAb 35 ± 4  
 αCCR-3 MoAb/αCCR-5 MoAb  33 ± 3 
 αCCR-1 MoAb/αCCR-3 MoAb/αCCR5 MoAb  19 ± 3 

Monocyte-derived DCs (106) were pretreated with stated MoAbs (10 μg/mL) for 30 minutes at 37°C and seeded on the filters precoated on the lower surface with 5 μg gelatin. The RANTES (1 μg/mL) used as chemoattractants were added to the lower chamber. After 2 hours of incubation, the migrated cells on the lower surface were visually counted.

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