Related Experiment Video
Updated: Apr 3, 2026

Subcellular Fractionation for ERK Activation Upon Mitochondrial-derived Peptide Treatment
Published on: September 25, 2017
The Pelargonium sidoides Extract EPs 7630 Drives the Innate Immune Defense by Activating Selected MAP Kinase Pathways
Katrin Witte1, Egon Koch2, Hans-Dieter Volk3
1Interdisciplinary Group of Molecular Immunopathology, Dermatology/Medical Immunology, University Hospital Charité, Berlin, Germany; Berlin-Brandenburg Center for Regenerative Therapies, University Hospital Charité, Berlin, Germany.
Abstract:
Pelargonium sidoides is a medical herb and respective extracts are used very frequently for the treatment of respiratory tract infections. However, the effects of Pelargonium sidoides and a special extract prepared from its roots (EPs 7630) on human immune cells are not fully understood. Here we demonstrate that EPs 7630 induced a rapid and dose-dependent production of TNF-α, IL-6, and IL-10 by human blood immune cells. This EPs 7630-induced cytokine profile was more pro-inflammatory in comparison with the profile induced by viral or bacterial infection-mimicking agents. The search for EPs 7630 target cells revealed that T-cells did not respond to EPs 7630 stimulation by production of TNF-α, IL-6, or IL-10. Furthermore, pretreatment of T-cells with EPs 7630 did not modulate their TNF-α, IL-6, and IL-10 secretion during subsequent activation. In contrast to lymphocytes, monocytes showed clear intracellular TNF-α staining after EPs 7630 treatment. Accordingly, EPs 7630 predominantly provoked activation of MAP kinases and inhibition of p38 strongly reduced the monocyte TNF-α production. The pretreatment of blood immune cells with EPs 7630 lowered their secretion of TNF-α and IL-10 and caused an IL-6 dominant response during second stimulation with viral or bacterial infection-mimicking agents. In summary, we demonstrate that EPs 7630 activates human monocytes, induces MAP kinase-dependent pro-inflammatory cytokines in these cells, and specifically modulates their production capacity of mediators known to lead to an increase of acute phase protein production in the liver, neutrophil generation in the bone marrow, and the generation of adaptive Th17 and Th22 cells.
Insights
Pelargonium sidoides extract (EPs 7630) rapidly activates human monocytes, inducing pro-inflammatory cytokines. This immune cell modulation by EPs 7630 influences the body's response to infection.
Area of Science:
- Immunology
- Pharmacology
- Natural Products
Background:
- Pelargonium sidoides extracts are widely used for respiratory infections.
- The precise impact of Pelargonium sidoides extract (EPs 7630) on human immune cells remains unclear.
Purpose of the Study:
- To investigate the effects of EPs 7630 on human blood immune cells.
- To identify the specific immune cell types and signaling pathways involved in the EPs 7630 response.
Main Methods:
- Human blood immune cells were stimulated with EPs 7630.
- Cytokine production (TNF-α, IL-6, IL-10) was measured.
- MAP kinase activation and T-cell/monocyte responses were analyzed.
Main Results:
- EPs 7630 induced rapid, dose-dependent TNF-α, IL-6, and IL-10 production, primarily in monocytes.
- T-cells showed no significant cytokine response to EPs 7630.
- EPs 7630 activated MAP kinases in monocytes, with p38 inhibition reducing TNF-α production.
Conclusions:
- EPs 7630 activates human monocytes via MAP kinase pathways, inducing pro-inflammatory cytokines.
- Pre-treatment with EPs 7630 modulates immune cell responses to subsequent infection-mimicking stimuli.
- These findings elucidate the immunomodulatory mechanisms of EPs 7630 in respiratory tract infections.
More Related Videos
08:15Author Spotlight: Network Pharmacology and Molecular Docking to Decipher the Action of Jiawei Shengjiang San Against Diabetic Kidney Disease
Published on: May 10, 2024
08:49Identification of Mediators of T-cell Receptor Signaling via the Screening of Chemical Inhibitor Libraries
Published on: January 22, 2019
Related Concept Videos
MAPK Signaling Cascades
Mitogens and the Cell Cycle