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Targets of new immunosuppressants in renal transplantation
Although current immunosuppression is highly effective in avoiding acute rejection, it is associated with nephrotoxicity, cardiovascular morbidity, infection, and cancer. Thus, new drugs dealing with new mechanisms, as well as minimizing comorbidities, are warranted in renal transplantation. Few nov...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4089611/ https://www.ncbi.nlm.nih.gov/pubmed/25028624 http://dx.doi.org/10.1038/kisup.2011.12 |
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author | Cruzado, Josep M Bestard, Oriol Melilli, Eduardo Grinyó, Josep M |
author_facet | Cruzado, Josep M Bestard, Oriol Melilli, Eduardo Grinyó, Josep M |
author_sort | Cruzado, Josep M |
collection | PubMed |
description | Although current immunosuppression is highly effective in avoiding acute rejection, it is associated with nephrotoxicity, cardiovascular morbidity, infection, and cancer. Thus, new drugs dealing with new mechanisms, as well as minimizing comorbidities, are warranted in renal transplantation. Few novel drugs are currently under investigation in Phase I, II, or III clinical trials. Belatacept is a humanized antibody that inhibits T-cell co-stimulation and has shown encouraging results in Phase II and III trials. Moreover, two new small molecules are under clinical development: AEB071 or sotrastaurin (a protein kinase C inhibitor) and CP-690550 or tasocitinib (a Janus kinase inhibitor). Refinement in selecting the best combinations for the new and current immunosuppressive agents is probably the main challenge for the next few years. |
format | Online Article Text |
id | pubmed-4089611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-40896112014-07-11 Targets of new immunosuppressants in renal transplantation Cruzado, Josep M Bestard, Oriol Melilli, Eduardo Grinyó, Josep M Kidney Int Suppl (2011) Meeting Report Although current immunosuppression is highly effective in avoiding acute rejection, it is associated with nephrotoxicity, cardiovascular morbidity, infection, and cancer. Thus, new drugs dealing with new mechanisms, as well as minimizing comorbidities, are warranted in renal transplantation. Few novel drugs are currently under investigation in Phase I, II, or III clinical trials. Belatacept is a humanized antibody that inhibits T-cell co-stimulation and has shown encouraging results in Phase II and III trials. Moreover, two new small molecules are under clinical development: AEB071 or sotrastaurin (a protein kinase C inhibitor) and CP-690550 or tasocitinib (a Janus kinase inhibitor). Refinement in selecting the best combinations for the new and current immunosuppressive agents is probably the main challenge for the next few years. Nature Publishing Group 2011-08 2011-07-15 /pmc/articles/PMC4089611/ /pubmed/25028624 http://dx.doi.org/10.1038/kisup.2011.12 Text en Copyright © 2011 International Society of Nephrology |
spellingShingle | Meeting Report Cruzado, Josep M Bestard, Oriol Melilli, Eduardo Grinyó, Josep M Targets of new immunosuppressants in renal transplantation |
title | Targets of new immunosuppressants in renal transplantation |
title_full | Targets of new immunosuppressants in renal transplantation |
title_fullStr | Targets of new immunosuppressants in renal transplantation |
title_full_unstemmed | Targets of new immunosuppressants in renal transplantation |
title_short | Targets of new immunosuppressants in renal transplantation |
title_sort | targets of new immunosuppressants in renal transplantation |
topic | Meeting Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4089611/ https://www.ncbi.nlm.nih.gov/pubmed/25028624 http://dx.doi.org/10.1038/kisup.2011.12 |
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