Monoclonal Antibody to CD14, TLR4, or CD11b: Impact of Epitope and Isotype Specificity on ROS Generation by Human Granulocytes and Monocytes
Table 1
The capability of antibodies against CD14 affects the LPS-induced effects (the references are indicated inside the square brackets).
Clone (isotype)
Epitope
Influence on LPS-induced effects
References
Does
Does not
3C10 (mIgG2b) Effectiveness decreases when LPS concentration increases
E7–R14
(1) Suppress CD14 binding to LBP·Re-LPS Salmonella minnesota (1 ng/ml) as well as PMN priming for fMLP-triggered О2⋅−/ROS (2) Whole or F(ab)2 suppress О2⋅−/ROS production in monocytes challenged by Re-LPS Escherichia coli (1 ng/ml, 5% blood serum) (3) Prevent CD11b/CD18 mobilization to the cell surface in PMNs stimulated by Ra/Rb-LPS E. coli K12 (30 ng/ml, without serum)
(1) Suppress CD14 binding to LBP·Re-LPS (2) Decrease PMN priming by LPS from E. coli O55:B5 (10 ng/ml, 1% serum) or E. coli O111:B4 (10 ng/ml, 10% serum) (3) Inhibit phosphatidic acid generation in LPS-primed and fMLP-stimulated PMNs (4) Suppress LPS-dependent activation of p38 MAPK in human PMNs (5) Whole or Fab suppress LPS uptake by human monocytes
(1) Affect fMLP-triggered О2⋅−/ROS production from unprimed PMNs
(1) Prevent LBP·Re-LPS S. minnesota binding to CD14 (2) Abolish almost completely PMN priming by LBP·Re-LPS S. minnesota (1 ng/ml) for fMLP-triggered О2⋅−/ROS
(1) Suppress LPS-induced IL-8 production by human retinal pigment epithelial cells (2) Decrease PMN priming by S- or Re-LPS E. coli (100 ng/ml, 2% serum) for fMLP-triggered О2⋅−/ROS production