Histamine release in intact human skin by monocyte chemoattractant factor-1, RANTES, macrophage inflammatory protein-1α, stem cell factor, anti-IgE, and.

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Histamine release in intact human skin by monocyte chemoattractant factor-1, RANTES, macrophage inflammatory protein-1α, stem cell factor, anti-IgE, and codeine as determined by an ex vivo skin microdialysis technique  Lars J. Petersen, MDa, Klaus Brasso, MDb, Morten Pryds, MDb, Per S. Skov, PhDc  Journal of Allergy and Clinical Immunology  Volume 98, Issue 4, Pages 790-796 (October 1996) DOI: 10.1016/S0091-6749(96)70128-8 Copyright © 1996 Mosby, Inc. Terms and Conditions

FIG. 1 Histamine release by serial dilutions of anti-IgE (A), codeine (B), and SCF (C). Increasing concentrations of each compound produced a concentration-dependent release of histamine. Histamine is expressed as net total histamine release (picomoles in 20 minutes). Values are means ± SEM of eight (anti-IgE), seven (codeine), and five (SCF) experiments. Journal of Allergy and Clinical Immunology 1996 98, 790-796DOI: (10.1016/S0091-6749(96)70128-8) Copyright © 1996 Mosby, Inc. Terms and Conditions

FIG. 2 Kinetics of histamine release by anti-IgE (squares), codeine (circles), and SCF (triangles). For each experiment, peak histamine release in 10 consecutive samples, after intradermal injection of the secretagogue, was found. This value was set as 100%, and histamine concentrations in the remainder samples in that experiment were expressed relatively to that sample. Values are means ± SEM of 21 (anti-IgE), 25 (codeine), and 6 (SCF) experiments (see Methods section). Journal of Allergy and Clinical Immunology 1996 98, 790-796DOI: (10.1016/S0091-6749(96)70128-8) Copyright © 1996 Mosby, Inc. Terms and Conditions

FIG. 3 A semi-logarithmic diagram showing peak histamine release in three series of experiments after serial dilutions of MCP-1 (open bars), RANTES (filled bars), and MIP-1α (hatched bars), all compared with vehicle responses and the positive control, anti-IgE (400 U/ml), in that particular series of experiments. Neither MCP-1, nor RANTES, nor MIP-1α released significant amounts of histamine; peak histamine release by chemokines was similar to vehicle responses. In comparison, anti-IgE (400 U/ml) showed a significant peak release of 800 to 1000 nmol/L. Values are means ± SEM of seven (MCP-1) and six (RANTES and MIP-1α) investigations. Journal of Allergy and Clinical Immunology 1996 98, 790-796DOI: (10.1016/S0091-6749(96)70128-8) Copyright © 1996 Mosby, Inc. Terms and Conditions

FIG. 4 Effect of a brief incubation (10 minutes) with 50 μl of MCP-1 (10-6 mol/L), RANTES (10-6 mol/L), MIP-1α (10-6 mol/L), and SCF (5.4 × 10-10 mol/L) versus incubation with vehicle on total histamine release induced by intradermal injection of 25 μl of anti-IgE (400 U/ml) in human skin. Histamine release after preincubation with vehicle is set as 100%. SCF significantly (p < 0.05) potentiated anti-IgE–induced histamine release by 33%, whereas none of the chemokines modulated anti-IgE–induced histamine release. Values are means ± SEM of eight (MCP-1) and seven (RANTES, MIP-1α, and SCF) experiments. Journal of Allergy and Clinical Immunology 1996 98, 790-796DOI: (10.1016/S0091-6749(96)70128-8) Copyright © 1996 Mosby, Inc. Terms and Conditions