Clinical Drug Experience Knowledgebase

Regulatory T Cells in the Response to SIT in Allergic Rhinitis.

Patients The design was a one-year, randomized open-label parallel group study in which patients were randomized in a 1:1 ratio to receive SIT with Dermatophagoides pteronyssinus extract (Alutard SQ, ALK-Abello', Hørsholm, Denmark) or to observe with standard pharmacotherapy (control group).

The study participants included 50 house dust mite (HDM)-allergic children aged 9-13, who received SIT with Dermatophagoides pteronyssinus (Der p) extract for one year. These were compared with 21 HDM-allergic children aged 9-14 who served as controls. All children were of Han nationality and were recruited from the allergy clinic of Beijing TongRen Hospital. They had a history of HDM-induced moderate or severe rhino-conjunctivitis of at least three years duration. Each patient also had a positive skin prick test (SPT) result for Der p (ALK-Abello', Hørsholm, Denmark) with a wheal diameter of at least 6 mm, and were positive for specific immunoglobulin E (IgE) to Der p (Pharmacia CAP System, Pharmacia Diagnostics, Uppsala, Sweden), with a RAST value of at least 0.7 kU/L. Children with a history of asthma or atopic dermatitis were excluded. The children undergoing immunotherapy were matched to atopic donors for age, sex, SPT response to Der p, total IgE and specific IgE to Der p levels (Table 1). The study protocol was approved by our institutional review board for human studies and informed consent was obtained from all subjects.

Immunotherapy protocol Children undergoing subcutaneous immunotherapy were given Dermatophagoides pteronyssinus extract (Alutard SQ, ALK-Abello, Hørsholm, Denmark) according to a cluster protocol which we have described previously[15]. In the first six weeks, children underwent visits for up-dosing, receiving two injections one hour apart with an increasing dose every week. The highest concentration, given in the sixth week, had an allergenic activity of 100,000 SQ/ml and contained 9.8 μg/ml Der p1. After week six, the dosing interval was increased to one month and maintained until the end of the first year. For patients randomized to non-SIT group, persistent rhinitis was managed with pharmacotherapy including intranasal steroids and oral antihistamines. Intranasal steroids were kept at the same dose during the study and antihistamines were used as required. Blood samples were taken at the baseline and after one year treatment in both groups.

Clinical evaluation Symptoms of AR children were assessed by the Total 5 Symptom Score (T5SS), which includes rhinorrhea, sneezing, nasal congestion, and nasal and ocular pruritus. Each symptom was scored on a scale of 0-3 (0 = none, 3 = severe). Medication use was scored and recorded daily, as described previously [16]. Arbitrary scores were attributed to the drugs used (0.75 points for 1 puff of nasal corticosteroids and 1 points for 1 tablet of antihistamine). Patients were instructed to use local steroids only (plus antihistamines if they did not improve symptoms) and to report each administration or variation of the initial drug therapy in the diary. Patients were also instructed to stop drugs at least 7 days before blood sampling.

Flow cytometry Peripheral blood was obtained by venous puncture and collected into preservative-free heparin. Peripheral blood mononuclear cells (PBMCs) were isolated by means of Ficoll-Plaque Plus density gradient centrifugation (Amersham Biosciences, NJ, USA). For intracellular detection of cytokine, PBMCs (2 × 106 cells/mL) were stimulated with 10 μg/mL Der p1 (D. pteronyssinus major allergen 1, Indoor Biotechnologies, United Kingdom) for 24 hours. Twenty-five ng/mL phorbol 12-myristate 13-acetate (PMA), 1 μg/mL ionomycin and 1.7 μg/mL monensine were added at 37 °C for the final four hours of stimulation (all from Sigma, Missouri, USA).

For flow cytometry, PBMCs were surface stained at room temperature for 20 minutes with anti-CD4-PerCP and anti-CD25-PE, or isotype control (mouse IgG1-PerCP or IgG1-PE) (all from Beckman Coulter, CA, USA). For intracellular staining of Foxp3, cells were fixed and permeabilized with Foxp3 fixation/permeabilization buffer, then stained with anti-human Foxp3-FITC or isotype control (IgG1-FITC) (all from BioLegend, CA, USA). For the intracellular cytokine analysis, Der p1-stimulated PBMCs were surface stained with anti-CD3-APC and anti-CD8-PerCP, and fixed with 4% paraformaldehyde/PBS. After being permeabilized using FACS Permeabilizing Solution (BD Pharmingen, CA, USA), cells were incubated for 30 minutes at room temperature with anti-IL-4-PE plus anti-IFN-γ-FITC, or anti-IL-10-PE plus anti-IL-4-FITC, and each antibody was matched with a respective isotype IgG1 as a control (all from BD Pharmingen). Different T subsets were selected for detailed phenotypic analysis as follows: (1) Th1 cells: IFN-γ+IL-4-CD3+CD8- T cells; (2) Th2 cells: IL-4+IFN-γ-CD3+CD8- T cells; and (3) Tr1 cells: IL-10+IL-4-CD3+CD8- T cells. For each analysis, at least 20,000 events were collected. Analysis was conducted using a FACSCalibur flow cytometer (BD Biosciences, NJ, USA).

ELISA PBMCs were resuspended at 2 × 106 cells/mL in RPMI-1640 medium and stimulated with 10 μg/mL Der p1 (D. pteronyssinus major allergen 1, Indoor Biotechnologies, United Kingdom). Cultures were incubated for 6 days at 37 ºC in a humidified incubator containing 5% CO2. Supernatants from allergen-stimulated PBMCs cultures were assayed for the presence of IFN-γ, IL-4, and IL-10 by means of ELISA (R&D Systems, Minneapolis, USA).

Isolation of CD4+CD25high Treg cells Heparinized blood was obtained from each of eight recruited SIT-treated children and eight AR controls for cell isolation and functional analysis. After non-CD4+ cells in the PBMCs were removed by LD column with a biotin-antibody cocktail and antibiotin microbeads, CD4+ T cells were isolated from the PBMCs by negative selection, and CD4+CD25+ T cells were positively selected from the CD4+ T cells. Finally, CD25- fractions were recovered using a MS-magnetic column using a human CD4+CD25+ regulatory T cell isolation kit according to the manufacturer's instructions (Miltenyi Biotec, Germany). Cells with the highest CD25 expression (CD25high) were selected through incubation with a limiting quantity of anti-CD25 antibody beads (2 μl of anti-CD25 beads/107 cells)[17]. The mean purity of the isolated CD4+ was 95% (93-97%) and 76% (72-88%) for CD4+CD25high T cells being Foxp3-positive.

Suppressive capacity of CD4+CD25high Treg cells To evaluate the suppressive capacity of CD4+CD25high Treg cells, cell proliferation and cytokine were analyzed. CD4+CD25- T cells (responders) alone or mixed CD4+CD25- T cells and CD4+CD25high T cells (suppressors) at a ratio of 2:1 were cultured in a final volume of 200 µl RPMI-1640 medium with 10 µg/ml Der p1. Cultures were incubated for 6 days at 37 ºC in a humidified incubator with 5% CO2. Autologous irradiated PBMCs (3000 rad) were added at 2 × 105 as antigen-presenting cells to CD4+CD25- T cell cultures. In all cases, triplicate medium wells were included as negative controls. At day six, 100 µl of supernatant was removed for Th1 and Th2 cytokine (IFN-γ and IL-4) analysis with an ELISA kit (R&D Systems, Minneapolis, USA). Cell proliferation of CD4+CD25- T cells was then assessed using a WST-8 (modified tetrazolium salt) cell proliferation kit (Cell Counting Kit-8, Dojin, Japan) according to the manufacturers' protocols. The proliferation result was expressed as absorbance at 450nm of the culture medium.

Statistics Statistical significance between groups was analyzed using a Mann-Whitney test. The significance of intra-group pre- and post-therapy changes were determined using a nonparametric Wilcoxon matched pairs test. The correlation coefficient r was generated using the Pearson correlation. All analyses were performed using SPSS version 13.0 statistical software. A 5% significance level was used (α = 0.05), power (1- β) equal to 90%. All tests were 2-tailed, and P values of less than 0.05 were considered statistically significant.