Glomerulonephritis
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Mesh-terms: Adolescent; Adult; Anemia :: complications; Anemia :: physiopathology; Blood Pressure; Cardiac Output; Chronic Disease; Dye Dilution Technique; Female; Glomerulonephritis; Hematocrit; Human; Hypertension, Malignant; Hypertension, Renal :: etiology; Indocyanine Green :: diagnostic use; Male; Middle Aged; Polycystic Kidney Diseases; Uremia :: complications; Uremia :: physiopathology; Vascular Resistance;
Mesh-terms: Amyloidosis; Blood Proteins; Diabetes Mellitus; Drug Therapy; Glomerulonephritis; Immunodiffusion; Inulin; Kidney Function Tests; Kidney Glomerulus; Lupus; Nephritis; Nephrotic Syndrome; Pathology; Precipitin Tests; Prednisolone; Prednisone; Protein Denaturation; Proteinuria; Renal Veins; Thrombosis; Transferrin; Urine; p-Aminohippuric Acid;
Mesh-terms: Adult; Blood Urea Nitrogen; Creatinine :: blood; Glomerulonephritis; Glucose Tolerance Test; Goodpasture Syndrome; Growth Hormone :: blood; Human; Hyperinsulinism; Kidney Failure, Chronic :: blood; Magnesium :: blood; Male; Middle Aged; Nephritis :: genetics; Phosphates :: blood; Potassium :: blood; Pyelonephritis; Renal Dialysis; Sodium :: blood; Uremia :: blood;
First Department of Pathology, Kansai Medical University, Moriguchi City, Osaka 570, Japan.
Using various animal models for autoimmune diseases, we have found that autoimmune diseases are stem cell disorders. The transplantation of normal hemopoietic stem cells (HSCs) can be used to treat autoimmune diseases, whereas the transplantation of abnormal HSCs from autoimmune-prone mice to normal mice leads to the induction of autoimmune diseases in recipients. To elucidate the differences between normal and abnormal HSCs, we have established a new method for purifying pluripotent-HSCs (P-HSCs), and have compared the qualitative differences. Although normal P-HSCs cannot proliferate under major histocompatibility complex (MHC)-incompatible microenvironments (stromal cells), abnormal P-HSCs can proliferate under such conditions. In addition, the proliferation of abnormal P-HSCs is much faster than that of normal P-HSCs. These findings indicate that abnormal P-HSCs are more resilient than normal P-HSCs. Therefore, we propose that allogeneic bone marrow transplantation (BMT)(not autologous BMT) should be applied to the treatment of autoimmune diseases. human data on BMT in autoimmune diseases is reviewed, and the conditions essential for successful BMT, including tolerance induction, are discussed.
Mesh-terms: Animals; Autoimmune Diseases :: etiology; Autoimmune Diseases :: therapy; Bone Marrow Transplantation; Diabetes Mellitus, Type II :: therapy; Glomerulonephritis; Hematopoietic Stem Cell Transplantation; Human; Mice; Organ Transplantation; Stem Cells; Stromal Cells; Support, Non-U.S. Gov't; Thymus Gland :: transplantation;
Mesh-terms: Blood Chemical Analysis; Blood Urea Nitrogen; Diagnosis; Glomerulonephritis; Gout; Kidney Diseases; Kidney Function Tests; Nephrosclerosis; Neural Conduction; Peripheral Nervous System Diseases; Polycystic Kidney Diseases; Pyelonephritis; Septicemia; Staphylococcal Infections; Urinary Tract Infections;
