Local immunomodulation with Fas ligand-engineered biomaterials achieves allogeneic islet graft acceptance
暂无分享,去创建一个
Christopher T. Johnson | Andrés J. García | L. Shea | D. Headen | E. Yolcu | Hong Zhao | H. Shirwan | W. Bowen | Michael D. Hunckler | M. Coronel | C. Johnson | Min Tan | J. Weaver | P. Shrestha | K. Woodward | Devon Headen | María M. Coronel
[1] Christopher T. Johnson,et al. Vasculogenic hydrogel enhances islet survival, engraftment, and function in leading extrahepatic sites , 2017, Science Advances.
[2] C. Ricordi,et al. Bioengineering of an Intraabdominal Endocrine Pancreas. , 2017, The New England journal of medicine.
[3] C. Ricordi,et al. Bioengineering the Endocrine Pancreas: Intraomental Islet Transplantation Within a Biologic Resorbable Scaffold , 2016, Diabetes.
[4] T. Curiel,et al. Chronic mTOR inhibition in mice with rapamycin alters T, B, myeloid, and innate lymphoid cells and gut flora and prolongs life of immune‐deficient mice , 2015, Aging cell.
[5] Andrés J. García,et al. Microfluidic‐Based Generation of Size‐Controlled, Biofunctionalized Synthetic Polymer Microgels for Cell Encapsulation , 2014, Advanced materials.
[6] W. R. Taylor,et al. Vasculogenic bio-synthetic hydrogel for enhancement of pancreatic islet engraftment and function in type 1 diabetes. , 2013, Biomaterials.
[7] U. Boggi,et al. Long-Term (5 Years) Efficacy and Safety of Pancreas Transplantation Alone in Type 1 Diabetic Patients , 2012, Transplantation.
[8] Jay C. Sy,et al. Maleimide Cross‐Linked Bioactive PEG Hydrogel Exhibits Improved Reaction Kinetics and Cross‐Linking for Cell Encapsulation and In Situ Delivery , 2012, Advanced materials.
[9] C. Lacelle,et al. Pancreatic Islets Engineered with SA-FasL Protein Establish Robust Localized Tolerance by Inducing Regulatory T Cells in Mice , 2011, The Journal of Immunology.
[10] V. Rodrik-Outmezguine,et al. High-dose rapamycin induces apoptosis in human cancer cells by dissociating mTOR complex 1 and suppressing phosphorylation of 4E-BP1 , 2011, Cell cycle.
[11] Qingsheng Li,et al. The mTOR kinase determines effector versus memory CD8+ T cell fate by regulating the expression of transcription factors T-bet and Eomesodermin. , 2010, Immunity.
[12] Elizabeth A. Kruse,et al. Membrane-bound but not Secreted Fas Ligand Is Essential for Fas-Induced Apoptosis and Prevention of Autoimmunity and Cancer , 2009, Nature.
[13] R. Ahmed,et al. mTOR regulates memory CD8 T cell differentiation , 2009, Nature.
[14] I. T. Ten Berge,et al. Intragraft FOXP3 Protein or mRNA During Acute Renal Allograft Rejection Correlates With Inflammation, Fibrosis, and Poor Renal Outcome , 2009, Transplantation.
[15] Y. Sagiv,et al. Apoptosis as a mechanism of T‐regulatory cell homeostasis and suppression , 2008, Immunology and cell biology.
[16] G. Jhangri,et al. FOXP3 Expression in Human Kidney Transplant Biopsies Is Associated with Rejection and Time Post Transplant but Not with Favorable Outcomes , 2008, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.
[17] C. June,et al. Cutting Edge: Foxp3-Mediated Induction of Pim 2 Allows Human T Regulatory Cells to Preferentially Expand in Rapamycin1 , 2008, The Journal of Immunology.
[18] M. Márques,et al. Tacrolimus‐Induced Diabetes in Rats Courses with Suppressed Insulin Gene Expression in Pancreatic Islets , 2007, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.
[19] G. Eisenbarth,et al. Priming and effector dependence on insulin B:9-23 peptide in NOD islet autoimmunity. , 2007, The Journal of clinical investigation.
[20] A. Rudensky,et al. Regulatory T cells prevent catastrophic autoimmunity throughout the lifespan of mice , 2007, Nature Immunology.
[21] C. Loddenkemper,et al. Selective depletion of Foxp3+ regulatory T cells induces a scurfy-like disease , 2007, The Journal of experimental medicine.
[22] Philippe Morel,et al. International trial of the Edmonton protocol for islet transplantation. , 2006, The New England journal of medicine.
[23] M. Battaglia,et al. Rapamycin selectively expands CD4+CD25+FoxP3+ regulatory T cells. , 2005, Blood.
[24] Yuichiro Yamada,et al. Tacrolimus suppresses glucose-induced insulin release from pancreatic islets by reducing glucokinase activity. , 2005, American journal of physiology. Endocrinology and metabolism.
[25] Narendra P. Singh,et al. Cell membrane modification for rapid display of proteins as a novel means of immunomodulation: FasL-decorated cells prevent islet graft rejection. , 2002, Immunity.
[26] B. Malassagne,et al. Transgenic Expression of CD95 Ligand on Thyroid Follicular Cells Confers Immune Privilege upon Thyroid Allografts , 2001, The Journal of Immunology.
[27] R. Gorczynski,et al. Dendritic Cells Genetically Engineered to Express Fas Ligand Induce Donor-Specific Hyporesponsiveness and Prolong Allograft Survival1 , 2000, The Journal of Immunology.
[28] K. Okumura,et al. Induction of antigen-specific immunosuppression by CD95L cDNA-transfected 'killer' dendritic cells , 1999, Nature Medicine.
[29] R. Sherwin,et al. Control of Autoimmune Diabetes in NOD Mice by GAD Expression or Suppression in β Cells , 1999 .
[30] F. Dallegri,et al. Soluble Fas ligand is chemotactic for human neutrophilic polymorphonuclear leukocytes. , 1999, Journal of immunology.
[31] Å. Lernmark,et al. Auto- and alloimmune reactivity to human islet allografts transplanted into type 1 diabetic patients. , 1999, Diabetes.
[32] M. Monden,et al. Protection of islet allografts transplanted together with Fas ligand expressing testicular allografts , 1998, Diabetologia.
[33] C. Ricordi,et al. Long-Term Function (6 Years) of Islet Allografts in Type 1 Diabetes , 1997, Diabetes.
[34] G. Nabel,et al. Inhibition of the alloantibody response by CD95 ligand , 1997, Nature Medicine.
[35] D. Hanahan,et al. Fas ligand expression in islets of Langerhans does not confer immune privilege and instead targets them for rapid destruction , 1997, Nature Medicine.
[36] J. Pepose,et al. CD95 ligand (FasL)-induced apoptosis is necessary for corneal allograft survival. , 1997, The Journal of clinical investigation.
[37] C. Stoeckert,et al. Prevention of Islet Allograft Rejection with Engineered Myoblasts Expressing FasL in Mice , 1996, Science.
[38] D. Green,et al. Fas Ligand-Induced Apoptosis as a Mechanism of Immune Privilege , 1995, Science.
[39] S. Ju,et al. Fas(CD95)/FasL interactions required for programmed cell death after T-cell activation , 1995, Nature.
[40] Seamus J. Martin,et al. Cell-autonomous Fas (CD95)/Fas-ligand interaction mediates activation-induced apoptosis in T-cell hybridomas , 1995, Nature.
[41] S. Nagata,et al. Lethal effect of the anti-Fas antibody in mice , 1993, Nature.
[42] K. Haskins,et al. Acceleration of diabetes in young NOD mice with a CD4+ islet-specific T cell clone. , 1990, Science.
[43] Bart O. Roep,et al. T-cell clones from a type-1 diabetes patient respond to insulin secretory granule proteins , 1990, Nature.
[44] R. Negrin,et al. Differential impact of mammalian target of rapamycin inhibition on CD4+CD25+Foxp3+ regulatory T cells compared with conventional CD4+ T cells. , 2008, Blood.