Reversal of T1D and Rapid Reduction of β-Cell Stress by IL-10–Dependent MDSCs Induced by TLR4-Ab

Type 1 diabetes (T1D) is caused by the autoimmune destruction of insulin-producing pancreatic β-cells. We published that an IgG3 Toll-like receptor 4 (TLR4)/myeloid differentiation factor 2 (MD2) agonistic antibody (TLR4-Ab) reversed acute T1D in NOD mice by induction of myeloid-derived suppressor cells (MDSCs), but the mechanism of MDSC induction was unclear. Here we show that TLR4-Ab reversal of acute T1D induced profound intraislet immune and endocrine changes in single-cell RNA sequencing compared with controls. Islet-infiltrating S100A9+ cells significantly upregulated 18 genes associated with MDSCs, including Nos2, the gene responsible for inducible nitric oxide synthase (iNOS) production. TLR4-Ab treatment induced significant changes in β-cell gene expression, with markedly reduced endoplasmic reticulum stress and reduced unfolded protein response. Bone marrow (BM) cells cultured with TLR4-Ab, but not granulocyte macrophage–colony-stimulating factor or lipopolysaccharide, induced MDSCs that suppressed T cells, and blockade of iNOS activity eliminated T-cell suppression. Blockade of interleukin 10 (IL-10) signaling during BM differentiation prevented T-cell suppression induced by TLR4-Ab–MDSC, demonstrating a central role for IL-10 in TLR4-Ab–mediated MDSC development. Reporter cell assays demonstrated predominant endosomal signaling with TLR4-Ab, and soluble (not plate-bound) TLR4-Ab was necessary for MDSC induction. TLR4-Ab treatment of T1D therefore induces an IL-10–dependent immunoregulatory MDSC response, which significantly downregulates β-cell stress. Article Highlights Therapy with IgG3 Toll-like receptor 4 (TLR4)/myeloid differentiation factor 2 (MD2) agonistic antibody (TLR4-Ab) is a novel approach to type 1 diabetes (T1D) immunotherapy that targets the innate immune system by inducing immunoregulatory myeloid-derived suppressor cells (MDSCs). We sought to define the mechanisms by which TLR4-Ab induces MDSCs and how they reverse T1D. TLR4-Ab induction of MDSCs requires interleukin 10 signaling in the bone marrow, and MDSCs mediate suppression via inducible nitric oxide synthase. Induction of immunoregulatory MDSCs results in profound downregulation of β-cell endoplasmic reticulum stress and unfolded protein response associated with acute T1D. Establishing mechanisms by which TLR4-Ab reverses acute T1D defines new therapeutic pathways for human T1D that target innate immunity to restore immune tolerance.

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Journal
Diabetes
Published
2026-10-15
DOI
https://doi.org/10.2337/db26-0636
Primary Topic
Diabetes and associated disorders
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article
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article

Reversal of T1D and Rapid Reduction of β-Cell Stress by IL-10–Dependent MDSCs Induced by TLR4-Ab

Luke S. Heuer, Nicolle Martin, Kyle J. Bednar, William M. Ridgway et al.
Diabetes
Diabetes and associated disorders
article

Reversal of T1D and Rapid Reduction of β-Cell Stress by IL-10–Dependent MDSCs Induced by TLR4-Ab

Luke S. Heuer, Nicolle Martin, Kyle J. Bednar, William M. Ridgway, Ixchel M Urbano, Manuel Rojas, Weici Zhang, Bethany P. Cummings, Shana L. Cohen
article en

Abstract

Type 1 diabetes (T1D) is caused by the autoimmune destruction of insulin-producing pancreatic β-cells. We published that an IgG3 Toll-like receptor 4 (TLR4)/myeloid differentiation factor 2 (MD2) agonistic antibody (TLR4-Ab) reversed acute T1D in NOD mice by induction of myeloid-derived suppressor cells (MDSCs), but the mechanism of MDSC induction was unclear. Here we show that TLR4-Ab reversal of acute T1D induced profound intraislet immune and endocrine changes in single-cell RNA sequencing compared with controls. Islet-infiltrating S100A9+ cells significantly upregulated 18 genes associated with MDSCs, including Nos2, the gene responsible for inducible nitric oxide synthase (iNOS) production. TLR4-Ab treatment induced significant changes in β-cell gene expression, with markedly reduced endoplasmic reticulum stress and reduced unfolded protein response. Bone marrow (BM) cells cultured with TLR4-Ab, but not granulocyte macrophage–colony-stimulating factor or lipopolysaccharide, induced MDSCs that suppressed T cells, and blockade of iNOS activity eliminated T-cell suppression. Blockade of interleukin 10 (IL-10) signaling during BM differentiation prevented T-cell suppression induced by TLR4-Ab–MDSC, demonstrating a central role for IL-10 in TLR4-Ab–mediated MDSC development. Reporter cell assays demonstrated predominant endosomal signaling with TLR4-Ab, and soluble (not plate-bound) TLR4-Ab was necessary for MDSC induction. TLR4-Ab treatment of T1D therefore induces an IL-10–dependent immunoregulatory MDSC response, which significantly downregulates β-cell stress. Article Highlights Therapy with IgG3 Toll-like receptor 4 (TLR4)/myeloid differentiation factor 2 (MD2) agonistic antibody (TLR4-Ab) is a novel approach to type 1 diabetes (T1D) immunotherapy that targets the innate immune system by inducing immunoregulatory myeloid-derived suppressor cells (MDSCs). We sought to define the mechanisms by which TLR4-Ab induces MDSCs and how they reverse T1D. TLR4-Ab induction of MDSCs requires interleukin 10 signaling in the bone marrow, and MDSCs mediate suppression via inducible nitric oxide synthase. Induction of immunoregulatory MDSCs results in profound downregulation of β-cell endoplasmic reticulum stress and unfolded protein response associated with acute T1D. Establishing mechanisms by which TLR4-Ab reverses acute T1D defines new therapeutic pathways for human T1D that target innate immunity to restore immune tolerance.

Diabetes
AstraZeneca (Japan) (JP), University of California Davis Medical Center (US), University of California, Davis (US), Universidad del Rosario (CO)
Good health and well-being
Openalex Percentile: Top 15%
Diabetes and associated disorders
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