Immunomodulation Followed by Antigen-Specific Treg Infusion Controls Islet Autoimmunity.
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ABSTRACT: Optimal immune-based therapies for type 1 diabetes (T1D) should restore self-tolerance without inducing chronic immunosuppression. CD4+Foxp3+ regulatory T cells (Tregs) are a key cell population capable of facilitating durable immune tolerance. However, clinical trials with expanded Tregs in T1D and solid-organ transplant recipients are limited by poor Treg engraftment without host manipulation. We showed that Treg engraftment and therapeutic benefit in nonautoimmune models required ablative host conditioning. Here, we evaluated Treg engraftment and therapeutic efficacy in the nonobese diabetic (NOD) mouse model of autoimmune diabetes using nonablative, combinatorial regimens involving the anti-CD3 (αCD3), cycloph
SUBMITTER: Cabello-Kindelan C
PROVIDER: S-EPMC6971488 | biostudies-literature | 2020 Feb
REPOSITORIES: biostudies-literature
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