Abstract

Quinoline-3-carboxamides (Q compounds) are immunomodulatory compounds that have shown efficacy both in autoimmune disease and cancer. We have in here investigated the impact of one such compound, paquinimod, on the development of diabetes in the NOD mouse model for type I diabetes (T1D). In cohorts of NOD mice treated with paquinimod between weeks 10 to 20 of age and followed up until 40 weeks of age, we observed dose-dependent reduction in incidence of disease as well as delayed onset of disease. Further, in contrast to untreated controls, the majority of NOD mice treated from 15 weeks of age did not develop diabetes at 30 weeks of age. Importantly, these mice displayed significantly less insulitis, which correlated with selectively reduced number of splenic macrophages and splenic Ly6Chi inflammatory monocytes at end point as compared to untreated controls. Collectively, these results demonstrate that paquinimod treatment can significantly inhibit progression of insulitis to T1D in the NOD mouse. We propose that the effect of paquinimod on disease progression may be related to the reduced number of these myeloid cell populations. Our finding also indicates that this compound could be a candidate for clinical development towards diabetes therapy in humans.

Highlights

  • Type 1 Diabetes (T1D) is an autoimmune disorder that causes severe loss of pancreatic β-cells and insulin production [1]

  • Paquinimod treatment prevents development of diabetes in the non-obese diabetic (NOD) mouse To assess the preventive efficacy of paquinimod on diabetes development in female NOD mice, we treated groups of mice with daily doses of 0.04, 0.2, 1, and 5 mg/kg/day of paquinimod from week 10 of age until week 20 of age

  • The aim of this study was to investigate whether treatment of NOD mice with the immunomodulatory Q compound paquinimod would show efficacy on the development of diabetes

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Summary

Introduction

Type 1 Diabetes (T1D) is an autoimmune disorder that causes severe loss of pancreatic β-cells and insulin production [1]. The most prominent therapy offered to T1D patients is exogenous insulin administration. This treatment, remains suboptimal and fails to prevent severe complications of the disease. The non-obese diabetic (NOD) mouse model is a good model for T1D and while developing a more severe insulitis than commonly seen in the human disease, displays several characteristics common to human T1D [3,4,5].

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