Abstract
Background
CD8+ regulatory T cells (Treg) have been considered to be involved in a model of ocular-induced tolerance, known as anterior chamber-associated immune deviation (ACAID). The mechanisms of suppression by CD8+ T cells in ACAID remain only poorly understood. TGF-β1 is considered as an inhibitory cytokine for immunosuppression in some models. The production of TGF-β1 by CD8+ T cells in ACAID, and whether CD8+ T cells exert suppression through TGF-β1, is unknown.
Methods
The suppressive effect of CD8+ T cells in ACAID mice was determined by a local adoptive transfer (LAT) assay. The production of TGF-β1 by CD8+ T cells was measured by enzyme-linked immunosorbent assay (ELISA). Anti-TGF-β1 antibodies were used in the LAT assay to test if they could block the inhibitory effect of CD8+ T cells.
Results
CD8+ T cells from ACAID mice were shown to block the delayed-type hypersensitivity (DTH) response in an antigen-specific manner in a LAT assay. These CD8+ T cells secreted TGF-β1, and their suppression could partially be blocked by anti-TGF-β1 antibodies.
Conclusions
Our study confirms that CD8+ T cells from ACAID mice possess inhibitory properties. This population exerts part of its suppressive function via the production of TGF-β1.
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Acknowledgement
This study is supported by Project of International Cooperation in Science and Technology, Guangdong Province (2004B50301002, 2006A50107001); Key Project of National Natural Science Foundation (30630064); National Supporting Project of P.R. China (2007BAI18B10).
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All the listed authors have participated actively in the study, and have read and approved the submitted manuscript. None of the authors has any potential financial conflict of interest related to this manuscript.
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Liqiong Jiang and Hao He contributed equally to this work.
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Jiang, L., He, H., Yang, P. et al. Splenic CD8+ T cells secrete TGF-β1 to exert suppression in mice with anterior chamber-associated immune deviation. Graefes Arch Clin Exp Ophthalmol 247, 87–92 (2009). https://doi.org/10.1007/s00417-008-0947-8
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DOI: https://doi.org/10.1007/s00417-008-0947-8