Structure-guided design of an invariant natural killer T cell agonist for optimum protection from type 1 diabetes in non-obese diabetic mice

Authors

  • H. J. Blumenfeld,

    1. Laboratory of Autoimmune Diabetes, Robarts Research Institute
    2. Department of Microbiology and Immunology, Dental Science Building, University of Western Ontario, London, ON, Canada
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  • R. Tohn,

    1. Laboratory of Autoimmune Diabetes, Robarts Research Institute
    2. Department of Microbiology and Immunology, Dental Science Building, University of Western Ontario, London, ON, Canada
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  • S. M. M. Haeryfar,

    1. Department of Microbiology and Immunology, Dental Science Building, University of Western Ontario, London, ON, Canada
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  • Y. Liu,

    1. Department of Chemistry and Biochemistry, Benson Science Building, Brigham Young University, Provo, UT, USA
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  • P. B. Savage,

    1. Department of Chemistry and Biochemistry, Benson Science Building, Brigham Young University, Provo, UT, USA
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  • T. L. Delovitch

    Corresponding author
    1. Laboratory of Autoimmune Diabetes, Robarts Research Institute
    2. Department of Microbiology and Immunology, Dental Science Building, University of Western Ontario, London, ON, Canada
      Dr T. L. Delovitch, Robarts Research Institute, University of Western Ontario, 100 Perth Drive, London, ON N6A 5 K8, Canada. E-mail: del@robarts.ca
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Dr T. L. Delovitch, Robarts Research Institute, University of Western Ontario, 100 Perth Drive, London, ON N6A 5 K8, Canada. E-mail: del@robarts.ca

Summary

Because invariant natural killer T (iNK T) cells link innate and adaptive immunity, the structure-dependent design of iNK T cell agonists may have therapeutic value as vaccines for many indications, including autoimmune disease. Previously, we showed that treatment of non-obese diabetic (NOD) mice with the iNK T cell activating prototypic glycolipid α-galactosylceramide (α-GalCer) protects them from type 1 diabetes (T1D). However, α-GalCer is a strong agonist that can hyperactivate iNK T cells, elicit several side effects and has shown only limited success in clinical trials. Here, we used a structure-guided design approach to identify an iNK T cell agonist that optimally protects from T1D with minimal side effects. Analyses of the kinetics and function of a panel of synthetic α-GalCer fatty acyl chain derivatives (C8:0-C16:0) were performed in NOD mice. C16:0 elicited the highest protection from insulitis and T1D, which was associated with a higher frequency and survival of iNK T cells and enhanced activity of tolerogenic dendritic cells (DCs) in draining pancreatic lymph nodes (PLN), inability to transactivate NK cells and a more rapid kinetics of induction and recovery of iNK T cells from anergy. We conclude that the length and structure of the acyl chain of α-GalCer regulates the level of protection against T1D in mice, and propose that the extent of this protection depends on the relative capacity of the acyl chain to accommodate an endogenous spacer lipid of appropriate length and structure. Thus, our findings with the α-GalCer C16:0 derivative suggest strongly that it be considered as a lead glycolipid candidate in clinical trials of T1D.

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