Therapeutic approach to organ transplantation.

Renal transplantation is firmly established as the preferred treatment for many patients suffering from endstage renal disease. Nonetheless no absolute consensus has developed on how to achieve optimal immunosuppression, and many individual centres employing somewhat different protocols report excellent graft and patient survival. Immunological considerations, including antirejection therapy, are organized around a few general principles. The first consideration is careful patient preparation and, in the circumstance of living donor renal transplantation, selection of the best available ABO compatible, human leukocyte antigen (HLA) match in the event that several potential living related donors are available for organ donation. Second is a multitiered approach to immunosuppressive therapy similar in principle to that used in chemotherapy; several agents are used simultaneously, each of which is directed at a different molecular target within the allograft response (Figure 1, Table 1). Additive/synergistic effects are achieved through application of each agent at a relatively low dose, thereby limiting the toxicity of each individual agent while increasing the total immunosuppressive effect. Third is the principle that higher immunosuppressive drug doses and/or more individual immunosuppressive drugs are required to gain early engraftment and to treat established rejection than are needed to maintain immunosuppression in the long-term. Hence intensive induction and lower dose maintenance drug protocols are used. Fourth is careful investigation of each episode of post-transplant graft dysfunction, with the realization that most of the common causes of graft dysfunction, including rejection, can (and frequently do) coexist. Successful therapy therefore often involves several simultaneous therapeutic manoeuvres. Fifth, the appropriate reduction or withdrawal of an immunosuppressive drug when that drug's toxicity exceeds its therapeutic benefit.

[1]  L Timmermann,et al.  The mechanism of action of cyclosporin A and FK506. , 1996, Clinical immunology and immunopathology.

[2]  B. Kahan Development of synergistic immunosuppressive drug regimens based upon cyclosporine. , 1993, Kidney international. Supplement.

[3]  M. Suthanthiran,et al.  Synergism between the CD3 antigen- and CD2 antigen-derived signals. Exploration at the level of induction of DNA-binding proteins and characterization of the inhibitory activity of cyclosporine. , 1993, Transplantation.

[4]  S. Najjar,et al.  Negative transcriptional regulation of human interleukin 2 (IL-2) gene by glucocorticoids through interference with nuclear transcription factors AP-1 and NF-AT. , 1993, The Journal of clinical investigation.

[5]  D. Gjertson,et al.  Survival of nationally shared, HLA-matched kidney transplants from cadaveric donors. The UNOS Scientific Renal Transplant Registry. , 1992, The New England journal of medicine.

[6]  Tony Hunter,et al.  The regulation of transcription by phosphorylation , 1992, Cell.

[7]  S. Schreiber Immunophilin-sensitive protein phosphatase action in cell signaling pathways , 1992, Cell.

[8]  G. Baumann Molecular mechanism of immunosuppressive agents. , 1992, Transplantation proceedings.

[9]  M. Grilli,et al.  NF-kappa B subunit regulation in nontransformed CD4+ T lymphocytes. , 1992, Science.

[10]  C. Klee,et al.  Calcineurin phosphatase activity in T lymphocytes is inhibited by FK 506 and cyclosporin A. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[11]  C. Walsh,et al.  Cyclosporin-mediated inhibition of bovine calcineurin by cyclophilins A and B. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[12]  I. Screpanti,et al.  Glucocorticoid receptor-mediated suppression of the interleukin 2 gene expression through impairment of the cooperativity between nuclear factor of activated T cells and AP-1 enhancer elements , 1992, The Journal of experimental medicine.

[13]  M. Suthanthiran,et al.  INHIBITION OF INTERLEUKIN 2 RECEPTOR EXPRESSION IN NORMAL HUMAN T CELLS BY CYCLOSPORINE: DEMONSTRATION AT THE mRNA, PROTEIN, AND FUNCTIONAL LEVELS1,2 , 1992, Transplantation.

[14]  M. Suthanthiran,et al.  Differential regulation of transforming growth factor beta and interleukin 2 genes in human T cells: demonstration by usage of novel competitor DNA constructs in the quantitative polymerase chain reaction , 1991, The Journal of experimental medicine.

[15]  G. Crabtree,et al.  Nuclear association of a T-cell transcription factor blocked by FK-506 and cyclosporin A , 1991, Nature.

[16]  Stuart L. Schreiber,et al.  Calcineurin is a common target of cyclophilin-cyclosporin A and FKBP-FK506 complexes , 1991, Cell.

[17]  T. Strom,et al.  Abrogation of glucocorticoid-mediated inhibition of T cell proliferation by the synergistic action of IL-1, IL-6, and IFN-gamma. , 1991, Journal of immunology.

[18]  A. Allison,et al.  Lymphocyte‐Selective Cytostatic and Immunosuppressive Effects of Mycophenolic Acid in Vitro: Role of Deoxyguanosine Nucleotide Depletion , 1991, Scandinavian journal of immunology.

[19]  S. Schreiber,et al.  Chemistry and biology of the immunophilins and their immunosuppressive ligands. , 1991, Science.

[20]  R. Steinman,et al.  The effect of immunosuppressive agents on the induction of nuclear factors that bind to sites on the interleukin 2 promoter , 1990, The Journal of experimental medicine.

[21]  M. Karin,et al.  Transcriptional interference between c-Jun and the glucocorticoid receptor: Mutual inhibition of DNA binding due to direct protein-protein interaction , 1990, Cell.

[22]  M. Suthanthiran,et al.  Physiologic signaling in normal human T-cells: mRNA phenotyping by northern blot analysis and reverse transcription-polymerase chain reaction. , 1990, Cellular immunology.

[23]  G. Crabtree,et al.  Cyclosporin A specifically inhibits function of nuclear proteins involved in T cell activation. , 1989, Science.

[24]  S. Schreiber,et al.  A receptor for the immuno-suppressant FK506 is a cis–trans peptidyl-prolyl isomerase , 1989, Nature.

[25]  Nolan H. Sigal,et al.  A cytosolic binding protein for the immunosuppressant FK506 has peptidyl-prolyl isomerase activity but is distinct from cyclophilin , 1989, Nature.

[26]  D. Norman The clinical role of OKT3. , 1989, Cardiology clinics.

[27]  T. Strom,et al.  Glucocorticoids inhibit transcriptional and post-transcriptional expression of interleukin 1 in U937 cells. , 1987, Journal of immunology.

[28]  J. Soulillou,et al.  [Use of cyclosporin A after antilymphocyte serum in renal transplantation]. , 1985, Presse medicale.

[29]  R. Rubin,et al.  EVOLVING USE OF OKT3 MONOCLONAL ANTIBODY FOR TREATMENT OF RENAL ALLOGRAFT REJECTION , 1984, Transplantation.

[30]  D. Speicher,et al.  Cyclophilin: a specific cytosolic binding protein for cyclosporin A. , 1984, Science.

[31]  A. Dalke,et al.  Hypoxanthine-guanine phosphoribosyltransferase-independent toxicity of azathioprine in human lymphoblasts. , 1984, Biochemical pharmacology.

[32]  S. Arya,et al.  Dexamethasone-mediated inhibition of human T cell growth factor and gamma-interferon messenger RNA. , 1984, Journal of immunology.

[33]  T. Franklin,et al.  The inhibition of nucleic acid synthesis by mycophenolic acid. , 1969, The Biochemical journal.

[34]  Elion Gb Symposium on immunosuppressive drugs. Biochemistry and pharmacology of purine analogues. , 1967 .

[35]  H. Sollinger,et al.  RS-61443 : mechanism of action, experimental and early clinical results , 1991 .

[36]  T. Strom,et al.  Evidence that glucocorticosteroids block expression of the human interleukin-6 gene by accessory cells. , 1990, Transplantation.

[37]  J. Bach The mode of action of immunosuppressive agents. , 1975, Frontiers of biology.