Published online before print September 9, 2009
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||
production by CD4+ and CD8+ T cellsDepartment of Pathology, Laboratory of Immune Regulation in Department of Biomedical Sciences, and Tumor Immunity Medical Research Center, Seoul National University College of Medicine, Seoul, Korea
2. Correspondence: Department of Pathology and Biomedical Sciences, Seoul National University College of Medicine, 28 Yongon-dong, Chongno-gu, Seoul, 110-799, Korea. E-mail: doohyun{at}snu.ac.kr
ABSTRACT
HP results from the repeated inhalation of environmental antigens; however, the roles of CD4+CD25+ Treg cells in HP are unknown. Therefore, we investigated the functions of CD4+CD25+ Treg cells in SR-induced murine HP. More severe HP was observed in CD4+CD25+ Treg cell-depleted mice than in control mice in terms of histological alterations, inflammatory cell numbers in BALF, and the serum level of SR-specific IgG, which were restored by the adoptive transfer of CD4+CD25+ Treg cells. The CD4+CD25+ Treg cell-depleted mice also showed elevated levels of IFN-
, TGF-β, and reduced IL-4 production in the lungs. Moreover, IL-10 production of CD4+CD25+ Treg cells and direct contact between CD4+CD25+ Treg cells and CD4+ or CD8+ T cells in BALF resulted in reduced IFN-
production. Taken together, CD4+CD25+ Treg cells play a protective role in SR-induced HP by suppressing IFN-
production by T cells.
Key Words: Treg cells suppression IL-10 INF-
Saccharopolyspora recti-virgula