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Articles tagged "Tolerance"

  • 2016 American Transplant Congress

    Lymph Node Stromal Laminins Differentially Regulate T Cell Immunity and Tolerance.

    T. Simon, J. Bromberg.

    University of Maryland, Baltimore, MD.

    Background:Our recent work demonstrated that laminins α4β1γ1 and α5β1γ1, components of the lymph node (LN) stroma, are differentially regulated. Tolerance is associated with relatively higher…
  • 2016 American Transplant Congress

    Rapamycin Prolongs Cardiac Allograft Survival in a Mouse Model by Inducing Myeloid-Derived Suppressor Cells.

    T. Nakamura, K. Masuda, T. Matsuyama, H. Ushigome, N. Yoshimura.

    Department of Organ Transplantation and General Surgery, Kyoto Prefectural University of Medicine, Kyoto, Japan.

    Mammalian target of rapamycin (mTOR) inhibitors are the main immunosuppressive drugs for organ transplant recipients. Nevertheless, the mechanisms by which mTOR inhibitors induce immunosuppression is…
  • 2016 American Transplant Congress

    Acquired Down-Regulation of B Cell Function Induced by Donor Blood Group Antigens After ABO-Incompatible Kidney Transplantation.

    M. Tasaki,1 K. Saito,1 Y. Nakagawa,1 N. Imai,2 T. Aoki,3 M. Kamimura,3 K. Takahashi,1 Y. Tomita.1

    1Division of Urology, Department of Regenerative & Transplant Medicine, Niigata Graduate School of Medical and Dental Sciences, Niigata, Japan; 2Division of Clinical Nephrology and Rheumatology, Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan; 3Division of Transfusion Medicine and Regenerative Medicine Bioscience Medical Center, Niigata University Medical and Dental Hospital, Niigata, Japan.

    Background: The long-term of B cell immunobiology against donor blood group antigen has not been elucidated in ABO incompatible kidney transplantation (ABOi KTx).Methods: The antibody…
  • 2016 American Transplant Congress

    Erythropoietin (EPO) Mediates Spontaneous Kidney Transplant Tolerance in Mice.

    P. Cravedi,1 C. Purroy,1 J. Madsen,2 R. Fairchild,3 T. Tanaka,3 W. Baldwin 3rd,3 A. Alessandrini,2 P. Heeger.1

    11Icahn School of Medicine at Mount Sinai, New York, NY; 2Transplantation Biology Research Center, Department of Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA; 33Department of Immunology, Cleveland Clinic Foundation, Cleveland.

    Spontaneous allogeneic kidney transplant tolerance occurs in mice, but the underlying mechanisms are unknown. Building upon recent human data showing that EPO, an erythropoietic hormone…
  • 2016 American Transplant Congress

    Rapamycin Nanotherapy Delays Heart Transplant Rejection.

    M. Braza,1 M. Lameijer,1 C. Perez-Medina,1 T. Reiner,3 M. Nahrendorf,4 Z. Fayad,1 R. Duivenvoorden,1 J. Ochando,2 W. Mulder.1

    1Translational and Molecular Imaging Institute, Icahn School of Medicine at Mount Sinai, New York; 2Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York; 3Radiology, Memorial Sloan-Kettering Cancer Center, New York; 4Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston.

    Background:In patients, allograft survival requires a cocktail of immunosuppressive drugs, while experimentally antibodies targeting the innate immune system have been shown to induce long-term tolerance,…
  • 2016 American Transplant Congress

    PD-L1/PD-L2-Expressing B-1a Cells Inhibit Allo-Reactive T Cells in Mice.

    T. Hirose,1,2 Y. Tanaka,1 H. Ohdan.1

    1Transplant Surgery, Hiroshima University, Hiroshima, Japan; 2Urology, Hokkaido University, Sapporo, Hokkaido, Japan.

    Donor lymphocyte infusion (DLI) induces donor-specific hypo responsiveness or immune-tolerance among allo-reactive T cells in different organ transplantation models. However, the optimal cell source or…
  • 2016 American Transplant Congress

    iNKT Cell Activation Under Co-Stimulatory Blockade Establishes Mixed Chimerism Through Thymic Regulatory T Cell Activation.

    T. Hirai,1 Y. Ishii,2 R. Ishii,1 S. Miyairi,1 M. Ikemiyagi,1 M. Okumi,1 K. Tanabe.1

    1Department of Urology, Tokyo Women's Medical University, Shinjuku, Tokyo, Japan; 2Laboratory for Vaccine Design, RIKEN-IMS, Yokohama, Kanagawa, Japan.

    Background: Invariant natural killer T (iNKT) cells have recently garnered considerable attention for their potential to induce regulatory T cells (Tregs). We previously reported a…
  • 2016 American Transplant Congress

    Three-Year Outcome After HSCT with Subsequent KT from the Same Haploidentical Donor without Immunosuppression.

    C. Schwarz,1 A. Lawitschka,2 G. Böhmig,3 E. Dauber,4 H. Greinix,5 N. Kozakowski,6 F. Mühlbacher,1 G. Berlakovich,1 T. Wekerle.7

    1Dept. of Surgery, Div. of Transplantation, Medeical University of Vienna, Vienna, Austria; 2St. Anna Children's Hospital, Vienna, Austria; 3Dept. of Internal Medicine, Division of Nephrology, Medical University of Vienna, Vienna, Austria; 4Dept. of Transfusion Medicine, Medical University of Vienna, Vienna, Austria; 5Dept of Internal Medicine, Div of Hematology, Medical University of Graz, Graz, Austria; 6Dept. of Clinical Pathology, Medical University of Vienna, Vienna, Austria; 7Section of Transplantation Immunology, Dept. of Surgery, Medical University of Vienna, Vienna, Austria.

    Allogeneic hematopoietic stem cell transplantation (HSCT) can lead to donor-specific tolerance. Patients reported in the literature that underwent kidney transplantation (KT) after a previous HSCT…
  • 2016 American Transplant Congress

    Designing a Novel Highly Selective Immunoproteasome Inhibitor That Promotes Longterm Heart Allograft Acceptance While Inducing Immune Cell Exhaustion, Treg Induction and Memory Cell Suppression.

    E. Sula Karreci,1 A. Mihali,1 M. Uehara,1 A. Kurdi,1 L. Riella,1 R. Abdi,1 H. Fan,2 P. Singh,2 C. Nathan,2 G. Lin,2 J. Azzi.1

    1Transplantation Research Center, Harvard Medical School, Boston, MA; 2Department of Microbiology and Immunology, Weill Cornell Medicine, New York City, NY.

    The constitutive Proteasomes (c-20S) are ubiquitously expressed cellular proteases that degrade polyubiquitinated proteins and regulate cell functions. However, immunoproteasomes (IP or i-20S) are primarily expressed…
  • 2016 American Transplant Congress

    Mechanistic Insights into How Targeting of HDAC10 Promotes Foxp3+ Treg Cell Suppressive Activity, Gene Expression and Metabolism, and Enhances Allograft Survival.

    S. Dahiya,1 L. Wang,1 U. Beier,1,2 A. Angelin,1 R. Han,1 D. Wallace,1,2 W. Hancock.1,2

    1Children's Hospital of Philadelphia, Philadelphia; 2University of Pennsylvania, Philadelphia.

    Foxp3+ T-regulatory (Treg) cells are key regulators of immune responses that can result in unwarranted inflammation and promote allograft rejection. From a theoretical perspective, targeting…
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