| Literature DB >> 32812339 |
Poulami Majumder1, Yichuan Zhang2, Marcos Iglesias2, Lixin Fan3, James A Kelley1, Caroline Andrews4, Nimit Patel5, Jason R Stagno6, Byoung Chol Oh2, Georg J Furtmüller2, Christopher C Lai1, Yun-Xing Wang6, Gerald Brandacher2, Giorgio Raimondi2, Joel P Schneider1.
Abstract
Combination therapies that target multiple pathways involved in immune rejection of transplants hold promise for patients in need of restorative surgery. Herein, a noninteracting multiphase molecular assembly approach is developed to crystallize tofacitinib, a potent JAK1/3 inhibitor, within a shear-thinning self-assembled fibrillar peptide hydrogel network. The resulting microcrystalline tofacitinib hydrogel (MTH) can be syringe-injected directly to the grafting site during surgery to locally deliver the small molecule. The rate of drug delivered from MTH is largely controlled by the dissolution of the encapsulated microcrystals. A single application of MTH, in combination with systemically delivered CTLA4-Ig, a co-stimulation inhibitor, affords significant graft survival in mice receiving heterotopic heart transplants. Locoregional studies indicate that the local delivery of tofacitinib at the graft site enabled by MTH is required for the observed enhanced graft survival.Entities:
Keywords: hydrogels; immunotherapy; peptides; self-assembly; transplants
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Year: 2020 PMID: 32812339 PMCID: PMC7686956 DOI: 10.1002/smll.202002791
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 15.153