Related Experiment Video
Updated: Sep 19, 2025
In Vivo Augmentation of Gut-Homing Regulatory T Cell Induction
Published on: January 22, 2020
In Vivo Accumulation of Regulatory T Cells Using Eliglustat-Loaded Cryogels
Einat B Vitner1,2,3, Giovanni Bovone1, Wei-Hung Jung1,2
1John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, 02138, USA.
Regulatory T cells (Tregs) maintain immune homeostasis and their adoptive transfer is being widely explored to mitigate inflammatory and autoimmune conditions. Here a biomaterial is developed to accumulate Tregs at a specific anatomic location to bypass the need for ex vivo Treg isolation and adoptive transfer. It is first shown that eliglustat, an FDA-approved inhibitor of UDP-glucose ceramide glucosyltransferase, promotes Tregs from both naïve and activated CD4+ T cells in vitro. Click-crosslinked cryogels fabricated from alginate and collagen allow for a sustained release of CXCL10 or CXCL11, and when injected in subcutaneous tissues led to the enrichment of effector and memory T cells to the scaffolds. Loading eliglustat into these cryogels significantly enhances the local accumulation of Tregs in vivo. These findings demonstrate that eliglustat-loaded cryogels offer a simple yet effective biomaterial strategy to boost Treg directly in vivo, potentially providing a targeted method to treat various inflammatory and autoimmune diseases.
Regulatory T cells (Tregs) maintain immune homeostasis and their adoptive transfer is being widely explored to mitigate inflammatory and autoimmune conditions. Here a biomaterial is developed to accumulate Tregs at a specific anatomic location to bypass the need for ex vivo Treg isolation and adoptive transfer. It is first shown that eliglustat, an FDA-approved inhibitor of UDP-glucose ceramide glucosyltransferase, promotes Tregs from both naïve and activated CD4+ T cells in vitro. Click-crosslinked cryogels fabricated from alginate and collagen allow for a sustained release of CXCL10 or CXCL11, and when injected in subcutaneous tissues led to the enrichment of effector and memory T cells to the scaffolds. Loading eliglustat into these cryogels significantly enhances the local accumulation of Tregs in vivo. These findings demonstrate that eliglustat-loaded cryogels offer a simple yet effective biomaterial strategy to boost Treg directly in vivo, potentially providing a targeted method to treat various inflammatory and autoimmune diseases.
