Summary
In recent years, a large number of structurally diverse immunosuppressants have been discovered that are effective for the treatment of organ transplantation. Some of them are undergoing clinical trials and may soon enter into routine clinical practice. These compounds are either chemical entities obtained from natural sources/synthetic means or biomaterials such as monoclonal antibodies/gene products/proteins. They have been found to interfere at different stages of T cell activation and proliferation, and can be identified as inhibitors of nucleotide synthesis, growth factor signal transduction and differentiation. Newer strategies involving combination of new agents with traditional immunosuppressants, monoclonal antibodies and gene therapy offer enormous potential, not only for the investigation of mechanisms pertaining to graft rejection, but also for its therapeutic prevention.
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Abbreviations
- CTL:
-
Dcytotoxic T lymphocytes
- CsA:
-
cyclosporin A
- GVHD:
-
graft versus host disease
- PHA:
-
phytohemagglutinin
- DHODH:
-
dihydroorotate dehydrogenase
- HPLC:
-
high performance liquid chromatography
- PKM:
-
pokweed mitogen
- MLR:
-
mixed lymphocyte reaction
- DSG:
-
15, deoxyspergualin
- MHC:
-
major histocompatibility complex
- IFN:
-
interferon
- moab:
-
monoclonal antibodies
- rHu:
-
recombinant human
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Kundu, B., Khare, S.K. (1999). Recent advances in immunosuppressants. In: Jucker, E. (eds) Progress in Drug Research. Progress in Drug Research, vol 52. Birkhäuser, Basel. https://doi.org/10.1007/978-3-0348-8730-4_1
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