Multicomponent Injectable Hydrogels for Antigen‐Specific Tolerogenic Immune Modulation

• Published in: Advanced healthcare materials 2017-03, Vol.6 (6), p.np-n/a
• Main Authors: Verbeke, Catia S., Gordo, Susana, Schubert, David A., Lewin, Sarah A., Desai, Rajiv M., Dobbins, Jessica, Wucherpfennig, Kai W., Mooney, David J.
• Format: Article
• Language: English
• Subjects: alginate hydrogels; Animals; Antigens - chemistry; Antigens - pharmacology; antigen‐specific tolerance; Biomaterials; Biomedical materials; dendritic cells; Diabetes Mellitus, Experimental - immunology; Diabetes Mellitus, Experimental - pathology; Diabetes Mellitus, Experimental - therapy; Diabetes Mellitus, Type 1 - immunology; Diabetes Mellitus, Type 1 - pathology; Diabetes Mellitus, Type 1 - therapy; Enrichment; Gels; Hydrogels - chemistry; Hydrogels - pharmacology; Immune Tolerance - drug effects; immunotherapy; Lactic Acid - chemistry; Lactic Acid - pharmacology; Lymphocytes; Mathematical models; Mice; Mice, Inbred NOD; Peptides; Polyglycolic Acid - chemistry; Polyglycolic Acid - pharmacology; regulatory T cells; Surgical implants; T-Lymphocytes, Regulatory - immunology; T-Lymphocytes, Regulatory - pathology
• ISSN: 2192-2640; 2192-2659
• DOI: 10.1002/adhm.201600773

Biomaterial scaffolds that enrich and modulate immune cells in situ can form the basis for potent immunotherapies to elicit immunity or reëstablish tolerance. Here, the authors explore the potential of an injectable, porous hydrogel to induce a regulatory T cell (Treg) response by delivering a peptide antigen to dendritic cells in a noninflammatory context. Two methods are described for delivering the BDC peptide from pore‐forming alginate gels in the nonobese diabetic mouse model of type 1 diabetes: encapsulation in poly(lactide‐co‐glycolide) (PLG) microparticles, or direct conjugation to the alginate polymer. While particle‐based delivery leads to antigen‐specific T cells responses in vivo, PLG particles alter the phenotype of the cells infiltrating the gels. Following gel‐based peptide delivery, transient expansion of endogenous antigen‐specific T cells is observed in the draining lymph nodes. Antigen‐specific T cells accumulate in the gels, and, strikingly, ≈60% of the antigen‐specific CD4+ T cells in the gels are Tregs. Antigen‐specific T cells are also enriched in the pancreatic islets, and administration of peptide‐loaded gels does not accelerate diabetes. This work demonstrates that a noninflammatory biomaterial system can generate antigen‐specific Tregs in vivo, which may enable the development of new therapies for the treatment of transplant rejection or autoimmune diseases. A biomaterial system to expand antigen‐specific regulatory T cells (Tregs) for tolerance induction is described. A diabetes‐related peptide antigen is delivered locally to dendritic cells that are enriched within an injectable, noninflammatory hydrogel. Following subcutaneous administration in nonobese diabetic mice, a model of type 1 diabetes, antigen‐specific Tregs are enriched in the gels and in the pancreatic islets.