Literature DB >> 20136784

mTOR inhibition: the learning curve in kidney transplantation.

Matthew R Weir1, Fritz Diekmann, Stuart M Flechner, Yvon Lebranchu, Didier A Mandelbrot, Rainer Oberbauer, Barry D Kahan.   

Abstract

All immunosuppressive medications require a learning curve that enables clinicians to improve the therapeutic index of agents. Mammalian target of rapamycin (mTOR) inhibitors are potentially a less nephrotoxic form of immunosuppression than calcineurin inhibitors (CNIs) that has been used in kidney transplant recipients for more than two decades. This drug class has a novel immunosuppressive action, probably mediated in part through inhibition of growth receptor signaling mechanisms. In addition, it has a unique drug toxicity, which is partially dose-related. This medication class also possesses antiproliferative activity, which may be useful in-post-transplant patients with increased atherosclerotic and malignancy risks. mTOR inhibitors have been utilized for de novo immunosuppression with CNIs, corticosteroids, and antimetabolites. mTOR inhibitors also have been used as CNI-sparing agents both early and late post-transplant. Much debate remains over how to best utilize mTOR inhibition in kidney transplantation.

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Year:  2010        PMID: 20136784     DOI: 10.1111/j.1432-2277.2010.01051.x

Source DB:  PubMed          Journal:  Transpl Int        ISSN: 0934-0874            Impact factor:   3.782


  7 in total

Review 1.  Regulation of immune responses by mTOR.

Authors:  Jonathan D Powell; Kristen N Pollizzi; Emily B Heikamp; Maureen R Horton
Journal:  Annu Rev Immunol       Date:  2011-11-29       Impact factor: 28.527

2.  Rapamycin reverses elevated mTORC1 signaling in lamin A/C-deficient mice, rescues cardiac and skeletal muscle function, and extends survival.

Authors:  Fresnida J Ramos; Steven C Chen; Michael G Garelick; Dao-Fu Dai; Chen-Yu Liao; Katherine H Schreiber; Vivian L MacKay; Elroy H An; Randy Strong; Warren C Ladiges; Peter S Rabinovitch; Matt Kaeberlein; Brian K Kennedy
Journal:  Sci Transl Med       Date:  2012-07-25       Impact factor: 17.956

Review 3.  Targeting the intragraft microenvironment and the development of chronic allograft rejection.

Authors:  Olivier Dormond; Marc Dufour; Tatsuichiro Seto; Sarah Bruneau; David M Briscoe
Journal:  Hum Immunol       Date:  2012-08-03       Impact factor: 2.850

4.  mTOR Inhibition: A Promise for a Young Heart.

Authors:  Stefany B A Cau; Rita C Tostes
Journal:  Front Physiol       Date:  2012-02-22       Impact factor: 4.566

5.  Onset and progression of diabetes in kidney transplant patients receiving everolimus or cyclosporine therapy: an analysis of two randomized, multicenter trials.

Authors:  Claudia Sommerer; Oliver Witzke; Frank Lehner; Wolfgang Arns; Petra Reinke; Ute Eisenberger; Bruno Vogt; Katharina Heller; Johannes Jacobi; Markus Guba; Rolf Stahl; Ingeborg A Hauser; Volker Kliem; Rudolf P Wüthrich; Anja Mühlfeld; Barbara Suwelack; Michael Duerr; Eva-Maria Paulus; Martin Zeier; Martina Porstner; Klemens Budde
Journal:  BMC Nephrol       Date:  2018-09-19       Impact factor: 2.388

6.  Icotinib combined with rapamycin in a renal transplant recipient with epidermal growth factor receptor-mutated non-small cell lung cancer: A case report.

Authors:  Qiong Zhao; Yina Wang; Yemin Tang; Ling Peng
Journal:  Oncol Lett       Date:  2013-11-05       Impact factor: 2.967

7.  Conversion to sirolimus ameliorates cyclosporine-induced nephropathy in the rat: focus on serum, urine, gene, and protein renal expression biomarkers.

Authors:  José Sereno; Sara Nunes; Paulo Rodrigues-Santos; Helena Vala; Petronila Rocha-Pereira; João Fernandes; Alice Santos-Silva; Frederico Teixeira; Flávio Reis
Journal:  Biomed Res Int       Date:  2014-05-19       Impact factor: 3.411

  7 in total

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