CD137 Plays Both Pathogenic and Protective Roles in Type 1 Diabetes Development in NOD Mice

• Published in: The Journal of immunology (1950) 2017-05, Vol.198 (10), p.3857-3868
• Main Authors: Forsberg, Matthew H, Ciecko, Ashley E, Bednar, Kyle J, Itoh, Arata, Kachapati, Kritika, Ridgway, William M, Chen, Yi-Guang
• Format: Article
• Language: English
• Subjects: 4-1BB Ligand - antagonists & inhibitors; 4-1BB Ligand - metabolism; Accumulation; Animals; Beta cells; CD137 antigen; CD4 antigen; CD8 antigen; CD8-Positive T-Lymphocytes - immunology; Cell activation; Cell Proliferation; Diabetes; Diabetes mellitus; Diabetes Mellitus, Type 1 - immunology; Diabetes Mellitus, Type 1 - physiopathology; Disease Progression; Immunoregulation; Insulin-Secreting Cells - immunology; Ligands; Lymph nodes; Lymphocytes; Lymphocytes T; Mice; Mice, Inbred NOD; Mice, Transgenic; Pancreas; Rodents; T cell receptors; T-Lymphocytes, Regulatory - immunology; Transgenic mice; Tumor Necrosis Factor Receptor Superfamily, Member 9 - deficiency; Tumor Necrosis Factor Receptor Superfamily, Member 9 - genetics; Tumor Necrosis Factor Receptor Superfamily, Member 9 - immunology; Tumor Necrosis Factor Receptor Superfamily, Member 9 - metabolism
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.1601851

We previously reported that CD137 (encoded by ) deficiency suppressed type 1 diabetes (T1D) progression in NOD mice. We also demonstrated that soluble CD137 produced by regulatory T cells contributed to their autoimmune-suppressive function in this model. These results suggest that CD137 can either promote or suppress T1D development in NOD mice depending on where it is expressed. In this study, we show that NOD. CD8 T cells had significantly reduced diabetogenic capacity, whereas absence of CD137 in non-T and non-B cells had a limited impact on T1D progression. In contrast, NOD. CD4 T cells highly promoted T1D development. We further demonstrated that CD137 was important for the accumulation of β cell-autoreactive CD8 T cells but was dispensable for their activation in pancreatic lymph nodes. The frequency of islet-infiltrating CD8 T cells was reduced in NOD. mice in part because of their decreased proliferation. Furthermore, CD137 deficiency did not suppress T1D development in NOD mice expressing the transgenic NY8.3 CD8 TCR. This suggests that increased precursor frequency of β cell-autoreactive CD8 T cells in NY8.3 mice obviated a role for CD137 in diabetogenesis. Finally, blocking CD137-CD137 ligand interaction significantly delayed T1D onset in NOD mice. Collectively, our results indicate that one important diabetogenic function of CD137 is to promote the expansion and accumulation of β cell-autoreactive CD8 T cells, and in the absence of CD137 or its interaction with CD137 ligand, T1D progression is suppressed.