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Harnessing cellular therapeutics for type 1 diabetes mellitus: progress, challenges, and the road ahead.
Grattoni, Alessandro; Korbutt, Gregory; Tomei, Alice A; García, Andrés J; Pepper, Andrew R; Stabler, Cherie; Brehm, Michael; Papas, Klearchos; Citro, Antonio; Shirwan, Haval; Millman, Jeffrey R; Melero-Martin, Juan; Graham, Melanie; Sefton, Michael; Ma, Minglin; Kenyon, Norma; Veiseh, Omid; Desai, Tejal A; Nostro, M Cristina; Marinac, Marjana; Sykes, Megan; Russ, Holger A; Odorico, Jon; Tang, Qizhi; Ricordi, Camillo; Latres, Esther; Mamrak, Nicholas E; Giraldo, Jaime; Poznansky, Mark C; de Vos, Paul.
Afiliação
  • Grattoni A; Department of Nanomedicine, Houston Methodist Research Institute, Houston, TX, USA. agrattoni@houstonmethodist.org.
  • Korbutt G; Department of Surgery, Houston Methodist Hospital, Houston, TX, USA. agrattoni@houstonmethodist.org.
  • Tomei AA; Department of Radiation Oncology, Houston Methodist Hospital, Houston, TX, USA. agrattoni@houstonmethodist.org.
  • García AJ; Alberta Diabetes Institute, University of Alberta, Edmonton, Alberta, Canada.
  • Pepper AR; Department of Surgery, University of Alberta, Edmonton, Alberta, Canada.
  • Stabler C; Diabetes Research Institute, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Brehm M; Department of Biomedical Engineering, University of Miami, Miami, FL, USA.
  • Papas K; Department of Surgery, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Citro A; Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Shirwan H; Woodruff School of Mechanical Engineering and Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA, USA.
  • Millman JR; Department of Surgery, University of Alberta, Edmonton, Alberta, Canada.
  • Melero-Martin J; J. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL, USA.
  • Graham M; Diabetes Institute, University of Florida, Gainesville, FL, USA.
  • Sefton M; Program in Molecular Medicine, Diabetes Center of Excellence, University of Massachusetts Chan Medical School, Worcester, MA, USA.
  • Ma M; Department of Surgery, The University of Arizona, Tucson, AZ, USA.
  • Kenyon N; Diabetes Research Institute, IRCCS Ospedale San Raffaele, Milan, Italy.
  • Veiseh O; Department of Pediatrics, Ellis Fischel Cancer Center, School of Medicine, University of Missouri, Columbia, MO, USA.
  • Desai TA; Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine, St. Louis, MO, USA.
  • Nostro MC; Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO, USA.
  • Marinac M; Department of Cardiac Surgery, Boston Children's Hospital, Boston, MA, USA.
  • Sykes M; Department of Surgery, Harvard Medical School, Boston, MA, USA.
  • Russ HA; Harvard Stem Cell Institute, Cambridge, MA, USA.
  • Odorico J; Department of Surgery, University of Minnesota, Minneapolis, MN, USA.
  • Tang Q; Department of Veterinary Population Medicine, University of Minnesota, St. Paul, MN, USA.
  • Ricordi C; Institute of Biomedical Engineering, University of Toronto, Toronto, Ontario, Canada.
  • Latres E; Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, Ontario, Canada.
  • Mamrak NE; Department of Biological and Environmental Engineering, Cornell University, Ithaca, NY, USA.
  • Giraldo J; Diabetes Research Institute, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Poznansky MC; Department of Surgery, University of Miami Miller School of Medicine, Miami, FL, USA.
  • de Vos P; Department of Bioengineering, Rice University, Houston, TX, USA.
Nat Rev Endocrinol ; 2024 Sep 03.
Article em En | MEDLINE | ID: mdl-39227741
ABSTRACT
Type 1 diabetes mellitus (T1DM) is a growing global health concern that affects approximately 8.5 million individuals worldwide. T1DM is characterized by an autoimmune destruction of pancreatic ß cells, leading to a disruption in glucose homeostasis. Therapeutic intervention for T1DM requires a complex regimen of glycaemic monitoring and the administration of exogenous insulin to regulate blood glucose levels. Advances in continuous glucose monitoring and algorithm-driven insulin delivery devices have improved the quality of life of patients. Despite this, mimicking islet function and complex physiological feedback remains challenging. Pancreatic islet transplantation represents a potential functional cure for T1DM but is hindered by donor scarcity, variability in harvested cells, aggressive immunosuppressive regimens and suboptimal clinical outcomes. Current research is directed towards generating alternative cell sources, improving transplantation methods, and enhancing cell survival without chronic immunosuppression. This Review maps the progress in cell replacement therapies for T1DM and outlines the remaining challenges and future directions. We explore the state-of-the-art strategies for generating replenishable ß cells, cell delivery technologies and local targeted immune modulation. Finally, we highlight relevant animal models and the regulatory aspects for advancing these technologies towards clinical deployment.

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Nat Rev Endocrinol Assunto da revista: ENDOCRINOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Nat Rev Endocrinol Assunto da revista: ENDOCRINOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos