Spontaneous Blastogenesis Profiles and IL-2 Receptor Expression on Kidney Allograft

References

• Bach F. H., Sach D. H. Transplantation immunology. N Engl J Med 1987; 317: 489
   PubMedGoogle Scholar
• Bishop G. A., Hall B. M., Duggin G. G., Horvath J. S., Sheil AGR, Tiller D. J. Imtnunopathollogy of renal allograft rejection analyzed with monoclonal antibodies to mononuclear cell markers. Kidney Int 1986; 29: 708
   PubMed Web of Science ®Google Scholar
• Suthanthiran M., Garavoy M. R. Immunologic monitoring of the renal transplant recipients. Urol Clin N Am 1983; 10: 315
   PubMedGoogle Scholar
• Hersh E. M., Butler W. T., Rossen R. D. In vitro studies of the human response to organ allograft: Appearance and detection of circulating activation lymphocytes. J Immunol 1971; 107: 571
   PubMed Web of Science ®Google Scholar
• Vessella R. L., Pierce G. E., Barth R. F., Davis J. E., Whittier F. C. Correlation of spontaneous leukocyte blastogenesis with human renal allograft rejection. Transplant 1977; 23: 227
   Google Scholar
• Veimer R., Daniel V., Pomer S., Opelz G. B. B lymphocyte response as an indicator of acute renal transplant rejection: I. Immunoglobulin-secreting cells in peripheral blood. Transplant 1989; 48: 569
   PubMedGoogle Scholar
• Fung J. J., Zeevi A., Markus B., Zerbe A., Duquesnoy R. J. Dynamics of allospecific T lymphocyte infiltration in vascularized human al-lografts. Immunol Res 1986; 5: 149
   PubMed Web of Science ®Google Scholar
• Carlquist J. F., Hammod M. E., Yowell R. L., O'Connell J. B., Anderson J. L. Correlation between class II antigen (DR) expression and interleukin-induced lymphocyte proliferation during acute cardiac allograft rejection. Transplant 1990; 50: 582
   PubMedGoogle Scholar
• Zeevi A., Fung J., Zerbe A., et al. Allospecificity of activated T cells grown from endomyocardial biopsies from heart transplant patients. Transplant 1986; 41: 620
   PubMedGoogle Scholar
• Heidecke C. D., Brauer R., Schneider-Eicke J., Schilling T., Wolff S., Diamantstein T. Direct evidence of a functional separation of alloreactive T lymphocytes from bystander cells infiltrating rat allografts. Transplant 1990; 50: 101
   PubMedGoogle Scholar
• Hancock W. W., Lord R. H., Colby A. J., Diamantstein T., Rickles F. R., Dijkstra C., Hogg N., Tilney N. L. Identification of IL-2R + T cells and macrophages within rejecting rat cardiac allografts, and comparison of the effects of treatment with anti-IL-2r monoclonal antibody or cyclosporin. J Immunol 1987; 138: 164
   PubMedGoogle Scholar
• Hancock W. W., Kobzik L., Colby A. J., O'Hara C. J., Cooper A. G., Gpdleski J. J. Detection of lymphokines and lymphokine receptors in pulmonary sarcoidosis: Immunohistologic evidence that inflammatory macrophages express IL-2 receptors. Am J Pathol 1986; 123: 1
   PubMedGoogle Scholar
• Orosz C. G., Bishop D. K. Limiting dilution analysis of alloreactive T-cell status and distribution during allograft rejection. Hum Immunol 1990; 28: 72
   PubMedGoogle Scholar
• Ruers TJM, Schutte B., Van Der Linden C. J., Buurman W. A. Cellular proliferation at the site of organ allografts and the influence of immunosuppressive therapy. Transplant 1990; 50: 568
   PubMedGoogle Scholar
• Ruers TJM, Buurman W. A., Van Boxtel C. J., Van Der Linden C. J., Kootstra G. Immunohistological observation in rat kidney allografts after local steroid administration. J Exp Med 1987; 166: 1205
   PubMedGoogle Scholar
• Porter K. A. Renal transplantation. Pathology of the kidney, R.H. Heptinstall. Little, Brown, Boston 1983; 1455
   Google Scholar
• Colvin R. B. The pathogenesis of vascular rejection. Transplant Proc 1991; 23: 2052
   PubMedGoogle Scholar
• Beverley PCL. CD45 R expression on memory T cells. Immunol Today 1990; 11: 203
   PubMedGoogle Scholar
• Benvenuto R., Bachertoni A., et al. Enhanced production of in-terferon gamma by T lymphocytes cloned from rejected kidney grafts. Transplant 1991; 51: 887
   PubMedGoogle Scholar
• Akbar A. N., Salmon M., Janossy G. The synergy between naive and memory T cells during activation. Immunol Today 1991; 12: 184
   PubMedGoogle Scholar
• Llorente L., Mitjavila F., et al. IL-4 counteracts the stimulatory effects of IL-2 on B cell. Eur J Immunol 1990; 20: 1887
   PubMed Web of Science ®Google Scholar
• Duijvestijn A. M., Van Vriesman JCB. Chronic renal allograft rejection. Transplant 1991; 52: 195
   PubMedGoogle Scholar
• Cooksey G., Reeve R. S., Paterson A. D., Cotton R. E., Blarney R. W. Lymphocyte subpopulations in cytologic aspirates from human renal allografts. Transplant Proc 1985; 17: 630
   Google Scholar
• Thiel G., Lindmann J., Mihatsch M. J. Cyclosporin: Acute and Chronic Toxicity or Rejection?. Sandoz Pharma, Basle 1989
   Google Scholar
• Gillum D. M., Truong L., Tasby J. Characterization of the interstitial cellular infiltrate in experimental chronic cyclosporine neph-ropathy. Transplant 1990; 49: 793
   PubMedGoogle Scholar
• Mihatsch M. J., Thiel G., Ryffel B. Morphologic diagnosis of cyclosporine nephtotoxicity. Semin Diag Pathol 1988; 5: 104
   PubMedGoogle Scholar
• Dische F. E., Neuberger J., Keating J., Parsons V., Caline R. Y., Williams R. Kidney pathology in liver allograft recipients after long-term treatment with cyclosporine A. Lab Invest 1988; 58: 395
   PubMedGoogle Scholar
• Bohman S. O., Wilczek H. E., Reinholt F. P., Von Willebrand E., Hayry P. Immunopathological patterns in long-term renal al-lografts. Transplant 1991; 51: 610
   PubMedGoogle Scholar
• Sibley, Rynasiewicz J., Ferguson R. M., et al. Morphology of cy-closporine nephrotoxicity and acute rejection in patients immu-nosuppressed with cyclosporine and prednisone. Surgery 1983; 94: 225
   PubMed Web of Science ®Google Scholar
• Murray B. M., Paller M. S., Ferris T. F. Effect of cyclosporine administration on renal hemodynamics in conscious rats. Kidney Int 1985; 28: 767
   PubMed Web of Science ®Google Scholar
• Myers B. Y. Cyclosporine nephrotoxicity. Kidney Int 1986; 30: 964
   PubMed Web of Science ®Google Scholar
• Gerkens J. F. Cyclosporine treatment of normal rats produces a rise in blood pressure and decreased renal vascular response to nerve stimulation, vasoconstrictors and epithelium-dependent dilators. J Pharmacol Exp Ther 1989; 250: 1105
   PubMed Web of Science ®Google Scholar
• Kon V., Sugiura M., Inagami T., Harvie B. R., Ichikawa I., Hoover R. L. Role of endothelin in cyclosporine-induced glomerular dysfunction. Kidney Int 1990; 37: 1487
   PubMed Web of Science ®Google Scholar
• Perico N., Benigni A., Zoja C., Delaini F., Remuzzi G. Functional significance of exaggerated renal thromboxane A2 synthesis induced by cyclosporine A. Am J Physiol 1986; 251: 581
   Google Scholar
• Pober J. S., Cotran R. S. The role of endothelial cells in inflammation. Transplant 1990; 50: 537
   PubMed Web of Science ®Google Scholar