Emma Mortensen

ORCID: 0000-0002-5775-8993
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About
Contact & Profiles
Research Areas
  • Immune Cell Function and Interaction
  • Pediatric Hepatobiliary Diseases and Treatments
  • Diabetes and associated disorders
  • CRISPR and Genetic Engineering
  • Liver Disease Diagnosis and Treatment
  • CAR-T cell therapy research
  • Liver Diseases and Immunity
  • Pancreatic function and diabetes

Virginia Mason Medical Center
2022-2024

Benaroya Research Institute
2022-2024

Adoptive transfer of regulatory T cells (Tregs) is therapeutic in type 1 diabetes (T1D) mouse models. Tregs that are specific for pancreatic islets more potent than polyclonal preventing disease. However, the frequency antigen-specific natural extremely low, and ex vivo expansion may destabilize Tregs, leading to an effector phenotype. Here, we generated durable, engineered (EngTregs) from primary human CD4+ by combining FOXP3 homology-directed repair editing lentiviral cell receptor (TCR)...

10.1126/scitranslmed.abn1716 article EN Science Translational Medicine 2022-10-05

Adoptive regulatory T (Treg) cell therapy is predicted to modulate immune tolerance in autoimmune diseases, including type 1 diabetes (T1D). However, the requirement for antigen (ag) specificity optimally orchestrate tissue-specific, Treg cell-mediated limits effective clinical application. To address this challenge, we present a single-step, combinatorial gene editing strategy utilizing dual-locus, dual-homology-directed repair (HDR) generate and specifically expand ag-specific engineered...

10.1016/j.ymthe.2023.07.016 article EN cc-by-nc-nd Molecular Therapy 2023-07-22
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