Prevention and Cure of Autoimmune Diabetes in Nonobese Diabetic Mice by Continuous Administration of FTY720
Abstract
Background Treatment of nonobese diabetic (NOD) mice with FTY720 before the development of insulitis prevents the onset of diabetes. In this study, the authors investigated whether FTY720 treatment of NOD mice with established insulitis prevents the development of diabetes. Methods FTY720 (1 mg/kg) was administered continuously to euglycemic NOD mice starting at 14 or 23 weeks of age. A group of untreated, age-matched NOD mice served as controls. Mice with more than 300 mg/dL blood glucose on three consecutive measurements were considered diabetic. Results Diabetes developed in control mice starting at 13 weeks of age and reached 78% by 33 weeks of age. Mice at 14 and 23 weeks of age exhibited extensive insulitis that progressed with age. Continuous oral administration of FTY720 starting at either age completely prevented the development of diabetes. However, its withdrawal at 37 weeks of age led to abrupt diabetes onset. Pancreases of FTY720-treated diabetes-free mice showed peripheral insulitis, with strong insulin staining. The protection from diabetes was also achieved by intraperitoneal injection of FTY720 or sirolimus (1.5 mg/kg). Unlike FTY720, withdrawal of sirolimus did not induce diabetes. Continuous oral FTY720 (3 mg/kg) treatment in overtly diabetic NOD mice led to complete reversal of diabetes in 6 of 11 mice. The standard adoptive transfer study in NOD-severe combined immunodeficient mice showed that peripheral lymphoid organs of FTY720-treated mice contained di…
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FTY720 is a sphingosine-1-phosphate receptor agonist that blocks lymph node egress and has been shown to protect NOD mice from T1D.
“FTY720, a sphingosine-1-phosphate receptor agonist that blocks lymph node egress and has been shown to protect NOD mice from T1D21,22”
From An autoimmune stem-like CD8 T cell population drives type 1 diabetes (2022) · cites this paper as [21]
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The alliance of sphingosine-1-phosphate and its receptors in immunity
Rivera, J., Proia, R. L., & Olivera, A. (2008) · Nature Reviews Immunology · doi:10.1038/nri2400 · Cited by 616 · see citing works
An autoimmune stem-like CD8 T cell population drives type 1 diabetes
Gearty, S. V., Dündar, F., Zumbo, P., Espinosa-Carrasco, G., Shakiba, M., Sanchez-Rivera, F. J., Socci, N. D., Trivedi, P., Lowe, S. W., Lauer, P., et al. (2022) · Nature · doi:10.1038/s41586-021-04248-x · Cited by 257 · see citing works
- Authors
- Maki, T., Gottschalk, R., Ogawa, N., & Monaco, A. P.
- Affiliations
- Beth Israel Deaconess Medical Center (US)
- Corresponding author
- Maki, Takashi
- Venue
- Transplantation
- Published
- 2005-05
- Volume
- 79
- Issue
- 9
- Pages
- 1051-1055
- ISSN
- 0041-1337 (ISSN-L)
- OpenAlex
- W2041439348
- Cited by
- 68
- References
- 0
- Citations by year
- 2024: 1 · 2023: 2 · 2022: 1 · 2021: 4 · 2020: 4 · 2019: 2 · 2017: 2 · 2016: 2 · 2015: 1 · 2014: 3 · 2013: 2 · 2012: 7
- FWCI
- 3.23
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Transplantation (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Keywords
- fingolimod, type 1 diabetes, NOD mice, insulitis, rapamycin, diabetes prevention, diabetes reversal, immunomodulation, diabetogenic T cells, adoptive transfer, immunosuppression
- MeSH terms
- Fingolimod Hydrochloride, Administration, Oral, Animals, Diabetes Mellitus, Type 1, Disease Models, Animal, Female, Immunosuppressive Agents, Propylene Glycols, Sphingosine, Mice, Inbred NOD, Mice
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