APC dysfunction is correlated with defective suppression of T cell proliferation in human type 1 diabetes

• Published in: Clinical immunology (Orlando, Fla.) Fla.), 2009-03, Vol.130 (3), p.272-279
• Main Authors: Jin, Yulan, Chen, Xueqin, Podolsky, Robert, Hopkins, Diane, Makala, Levi H.C, Muir, Andy, She, Jin-Xiong
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Allergy and Immunology; Antigen presenting cells; Antigen-Presenting Cells - cytology; Antigen-Presenting Cells - immunology; Autoimmunity; Biological and medical sciences; CD4-Positive T-Lymphocytes - cytology; CD4-Positive T-Lymphocytes - immunology; Cell Proliferation; Cells, Cultured; Child; Child, Preschool; Diabetes Mellitus, Type 1 - immunology; Diabetes Mellitus, Type 1 - physiopathology; Diabetes. Impaired glucose tolerance; Endocrine pancreas. Apud cells (diseases); Endocrinopathies; Etiopathogenesis. Screening. Investigations. Target tissue resistance; Female; Fundamental and applied biological sciences. Psychology; Fundamental immunology; Humans; Infant; Interleukin-2 Receptor alpha Subunit - immunology; Lymphocyte Activation; Male; Medical sciences; Middle Aged; Regulatory T cells; Suppression; Type 1 diabetes; Young Adult
• ISSN: 1521-6616; 1521-7035
• DOI: 10.1016/j.clim.2008.10.005

Abstracts It is widely believed that CD4+ CD25+ regulatory T cells (Treg) are defective in type 1 diabetes (T1D) and other autoimmune diseases. However, this conclusion is based on the suboptimal in vitro suppression results from very small numbers of subjects. Furthermore, the cells responsible for the suboptimal suppression have not been defined. Therefore, we carried out extensive in vitro suppression assays using both autologous and heterologous donors of Tregs, effector T cells and antigen-presenting cells (APC) from both T1D patients and normal controls. Our in vitro suppression data indicated that a significantly higher proportion (40.0%) of T1D patients have “very low suppression” activity (defined as < 25%) by autologous Treg compared to controls (6.3%) ( p = 0.002). Meta-analysis of the published results confirmed this observation with 45.7% low suppressors in T1D and 7.8% in controls ( p = 0.00002). Interestingly, suppression assays using heterologous Tregs, effector T cells and APC suggest that the source of APC is correlated with the suppression activity. The frequencies of CD4+ CD25+ and CD4+ CD25hi T cells were found to increase with age in normal controls but not in T1D patients, resulting in significantly higher frequencies of CD4+ CD25+ ( p = 0.001) and CD4+ CD25hi ( p = 0.009) T cells in young T1D subjects than age-matched controls but slightly lower CD4+ CD25+ ( p = 0.003) and CD4+ CD25hi ( p = 0.08) T cells in old T1D subjects than age-matched controls.