Heme Oxygenase-1-Mediated CD4 super(+)CD25 super(high) Regulatory T Cells Suppress Allergic Airway Inflammation

• Published in: Journal of Immunology Vol. 177; no. 9; pp. 5936 - 5945
• Main Authors: Xia, Zhen-Wei, Zhong, Wen-Wei, Xu, Li-Qing, Sun, Jian-Le, Shen, Qing-Xiang, Wang, Ji-Guang, Shao, Jie, Li, Yun-Zhu, Yu, Shan-Chang
• Format: Journal Article
• Language: English
• Published: 01.11.2006
• ISSN: 0022-1767; 1365-2567

Heme oxygenase-1 (HO-1) has anti-inflammatory effects in asthma. CD4 super(+)CD25 super(high) regulatory T cells (Treg) are a potent immunoregulator that suppresses the immune response. We studied the effects of HO-1-mediated CD4 super(+)CD25 super(high) Treg on suppression of allergic airway inflammation by comparing mice treated with hemin, OVA, Sn-protoporphyrin (SnPP), and hemin plus SnPP. Airway responsiveness, airway eosinophil infiltration, the level of OVA-specific IgE, and the numbers of cells in general and eosinophils in particular in bronchial alveolar lavage fluid were lower in the hemin group than in the OVA, SnPP, and hemin plus SnPP groups. The expressions of HO-1 mRNA and protein in the lung were increased by repeated administrations of hemin and SnPP. However, the activity of HO-1 was highest in hemin mice. The percentage and suppressive function of CD4 super(+)CD25 super(high) Treg and the expression of Foxp3 mRNA were obviously enhanced after treatment with hemin. This increase was diminished by the administration of SnPP. The concentration of serum IL-10 was higher in the hemin group than in the other groups, whereas the level of serum TGF- beta did not significantly differ across groups. Furthermore, the ratio of IFN- gamma /IL-4 mRNA in the lung was higher in hemin-treated mice than in OVA and SnPP mice. The suppressive capacity of CD4 super(+)CD25 super(high) Treg was not enhanced in the IL-10-deficient mice treated with hemin. In conclusion, our experiments in the animal model demonstrated that HO-1 has anti-inflammatory effects, probably via enhancement of the secretion of IL-10 and promotion of the percentage of CD4 super(+)CD25 super(high) Treg.