Immunomodulatory properties of dilute drugs in human monocyte/macrophages cell line THP-1 as a model of dose-response effects

Background: Immunomodulatory properties are evoked by many highly diluted drugs and may be the base of complex systemic effects of the remedies in the organism. Monocyte/macrophages exert a pivotal role in innate immunity regulation and in inflammation. THP-1 cells have become one of most widely used cell lines to investigate the function and regulation of monocytes and macrophages. These cells resemble primary monocytes–macrophages isolated from donors in the vasculature, with the advantage of homogeneous genetic background that minimizes the degree of variability in the cell phenotype; this trait is particularly important when studying the biological function of chemicals with high dilutions [1]. Using this model we tested different doses/dilutions of homeopathic and allopathic drugs. Methodology: The cell line THP-1 derived from the blood of a patient with acute monocytic leukemia, resemble primary monocytes and macrophages in morphology and differentiation property. The cell line was provided by DSMZ Culture Collection and cultured in RPMI medium (Lonza) added with 10% (w/v) fetal bovine serum (FBS, Lonza) and 2mM ultraglutammine, at 37°C in controlled atmosphere (5% CO2, 95% air) and complete humidity. In all the experiments the cells were seeded in microplates (4103/well) in RMPI with 2% fetal bovine serum and exposed to phorbol-12-myristate-13-acetate (PMA, 20 ng/ml) for 48h. In this period, the THP-1 cells adhered to culture plates and differentiated into a macrophage phenotype with marked morphological changes (Figure 1). Concomitantly with the addition of immunoactive drugs, cells were activated with different doses of bacterial lipopolysaccharide (LPS, from 0 to 100 ng/ml) and incubated for 24h. Figure 1: Pics of THP-1 cells without (left) and with PMA treatment (right). Betamethasone (Bentelan) was diluted/succussed in sterile water and added to cells at concentrations ranging from 0.01 to 100 ng/ml. Gelsemium sempervirens centesimal dilutions (c), 2c, 3c, 4c, 5c, 9c and 30c, and the corresponding controls were freshly prepared in glass tubes starting from 30% ethanol solutions (provided by Laboratoires Boiron and prepared following the French Pharmacopoeia) by 100x dilution in pure water and agitated in automatic dynamizer (see detail in [2]). The drugs were kept in the LPS-activated cells for 24 h. The dosage of pro-inflammatory (TNF-a, IL-6 and IL-1b) and anti-inflammatory (IL-10) cytokines was monitored by immune detection with ELISA assays (eBioscience) starting from the culture supernatants. The variation of viability and cell density were examined by WST assay and by quantification of total protein with Bradford assay on lysed cells, respectively. Repeated experiments were conducted in microplates, being careful to perform analogous manipulations to the drug dilutions and the corresponding controls. Statistical analysis was performed with paired T-test. Results and discussion: After stimulation with different doses of LPS, the responses of THP-1 cells can be monitored via the dosage of specific interleukins. The production of IL-1β (as proof) in response to different doses of LPS is shown in Figure 2. The cell model is very sensitive to variations in the amount of activator, exponentially increasing the amount of cytokine produced. The same was observed for the other cytokines investigated. The experiments with the immunoactive drugs were performed in intermediate condition of activation, that looked adequate to observe both increase and inhibition effects. Figure 2. Quantification of the cytokine IL-1β produced in THP-1 cell supernatants after activation with increasing concentrations of LPS, in presence or not of interferon- as co-activator. Histograms report mean values ± SD. Betamethasone, a potent glucocorticoid steroid with anti-inflammatory and immunosuppressive properties, was used as model immunomodulatory drug. Figure 3 describes the effects of different doses of the steroid on LPS-activated cells. Notably, we tested the effect of “physiological” doses of betamethasone in circulating blood and some of the doses that can be relevant in pharmacokinetics of the drugs (the therapeutic dosage in human correspond to the dose of 0.2 μM). As shown in Figure 3, the concentration of the proinflammatory cytokine TNF-α and IL-6 decreases linearly with the increase of the betamethasone dose, in particular when the cells were strongly stimulated with LPS (100 ng/ml). In contrast, if the LPS stimulus is weaker (LPS 10 ng/ml) the direction of effect depends on the dose of betamethasone: low doses (0.01 and 0.1 μM) seem to increase the concentration of TNF-α, while larger doses exert a inhibitory action, as expected (Figure 3A). This effect can be described as a typical hormetic behavior and it was observed also in the left part of Figure 3C, where the IL-10 production is increased with low doses of the immunosuppressive drug. Notably, in the case of IL-10, the steroid did not impair significantly the cytokine production in THP-1 cells activated with LPS 100 ng/ml. Actually, the activation pathway of the pro-inflammatory cytokine IL-10 is different from the TNF-α [3]. Figure 3. Effects of betamethasone on the production of the pro-inflammatory cytokines TNF-α and IL-6 and the anti-inflammatory cytokine IL-10. The dose response experiments were performed both in presence of LPS 10 or 100 ng/ml as cell activator. Bars report mean value ± SEM. The effects on THP-1 macrophages of Gelsemium sempervirens (2c, 3c, 4c, 5c, 9c and 30c) were compared with the corresponding potentized vehicles in cells activated with either high LPS dose (100 ng/ml) or low dose (10 ng/ml). Figure 4 shows the main results concerning three cytokines. This compound was tested both to extend our previous knowledge gathered with neuronal models [2] and because it is often used in influenza syndromes and in the Materia medica it is associated with symptoms of fever and inflammation. Figure 4. Percentage effect of Gelsemium s. treatment vs the corresponding succussed control at different dilutions on the THP-1 cytokine production. The variation of the cytokines concentration was measured in the supernatants of cells after 24h of treatment by ELISA assay. Values in graphs are mean % effect ± SEM, n=12, two replicated experiments. As shown in Figure 4A and 4B, the pro-inflammatory cytokines IL-6 and TNF-α were apparently modulated by Gelsemium s., although not in a linear fashion with increasing concentration. Analogous trends were obtained in the two LPS conditions. The highest doses (low dilutions) increased slightly the cytokine production (Gels 2c and 3c), while a maximum of inhibition was observed with 4c and 5c dilutions. Statistical inference was obtained in the data from the separate experiments for the TNF-α inhibition with Gels 4c (p