We sought to examine the effect of grass pollen injection immunotherapy on the numbers of Foxp3+CD4+ and Foxp3+CD25+ T cells in and out of season and their expression of IL-10 in the nasal mucosa of patients with hay fever.
Nasal biopsy specimens were obtained from untreated patients with hay fever, participants with grass pollen allergy who had received 2 years of immunotherapy, and healthy control subjects. Dual-immunofluorescence microscopy was used to enumerate and colocalize Foxp3 expression to CD4+ and CD25+ T cells in the nasal mucosa. Triple staining was performed to colocalize Foxp3+ cells to CD3+CD25+ and CD3+ IL-10–expressing cells.
At peak season, numbers of Foxp3+CD25+ (P = .02) and Foxp3+CD4+ (P = .03) cells were significantly increased in the nasal mucosa of immunotherapy-treated patients compared with numbers before treatment. Foxp3+CD25+ (P = .03) and Foxp3+CD4+ (P = .04) cells were also greater in immunotherapy-treated patients out of season compared with those in untreated patients with hay fever. Within the immunotherapy-treated group, 20 % of CD3+CD25+ cells expressed Foxp3, and 18 % of Foxp3+CD3+ cells were IL-10 positive.
The presence of local Foxp3+CD25+CD3+ cells in the nasal mucosa, their increased numbers after immunotherapy, and their association with clinical efficacy and suppression of seasonal allergic inflammation support a putative role for Treg cells in the induction of allergen-specific tolerance in human subjects.