Literature DB >> 29603637

Carpe diem-Time to transition from empiric to precision medicine in kidney transplantation.

Chris Wiebe1,2, Julie Ho1,3, Ian W Gibson2,4, David N Rush1, Peter W Nickerson1,3,2.   

Abstract

The current immunosuppressive pipeline in kidney transplantation is limited. In part, this is due to excellent one-year allograft outcomes with the current standard of care (ie, calcineurin inhibitor in combination with anti-proliferative agents). Despite this success, a recent Federal government-sponsored systematic review has identified gaps/limits in the evidence of what constitutes optimal calcineurin inhibitor use in the short- and long-term. Moreover, recent empiric approaches to minimize/withdraw/convert from calcineurin inhibitors have come with the price of increased alloreactivity. As the time horizon to replace calcineurin inhibitors on a global scale may be distant, the transplant community should seize the opportunity to develop ways to personalize calcineurin inhibitor immunosuppression to the individual-transitioning from empiricism to precision. The authors argue in this viewpoint that the path to precision will require measures capable of detecting subclinical alloreactivity to define adequacy of immunosuppression, as well as novel genetic analytics to accurately define alloimmune risk at the individual level-both approaches will require validation in clinical trials.
© 2018 The American Society of Transplantation and the American Society of Transplant Surgeons.

Entities:  

Keywords:  basic (laboratory) research/science; clinical research/practice; graft survival; histocompatibility; immunosuppression/immune modulation; immunosuppressive regimens; kidney transplantation/nephrology; major histocompatibility complex (MHC); monitoring: immune; risk assessment/risk stratification

Mesh:

Substances:

Year:  2018        PMID: 29603637     DOI: 10.1111/ajt.14746

Source DB:  PubMed          Journal:  Am J Transplant        ISSN: 1600-6135            Impact factor:   8.086


  5 in total

1.  Dual JAK2/Aurora kinase A inhibition prevents human skin graft rejection by allo-inactivation and ILC2-mediated tissue repair.

Authors:  Kelly Walton; Kirsti Walker; Megan Riddle; Brent H Koehn; Jordan Reff; Elizabeth M Sagatys; Michael A Linden; Joseph Pidala; Jongphil Kim; Marie C Lee; John V Kiluk; Jane Yuet Ching Hui; Sang Y Yun; Yan Xing; Heather Stefanski; Harshani R Lawrence; Nicholas J Lawrence; Jakub Tolar; Claudio Anasetti; Bruce R Blazar; Said M Sebti; Brian C Betts
Journal:  Am J Transplant       Date:  2021-11-08       Impact factor: 9.369

2.  HLA-DR/DQ molecular mismatch: A prognostic biomarker for primary alloimmunity.

Authors:  Chris Wiebe; Vasilis Kosmoliaptsis; Denise Pochinco; Ian W Gibson; Julie Ho; Patricia E Birk; Aviva Goldberg; Martin Karpinski; Jamie Shaw; David N Rush; Peter W Nickerson
Journal:  Am J Transplant       Date:  2018-12-15       Impact factor: 8.086

3.  Multicentre randomised controlled trial protocol of urine CXCL10 monitoring strategy in kidney transplant recipients.

Authors:  Julie Ho; Atul Sharma; Kristine Kroeker; Robert Carroll; Sacha De Serres; Ian W Gibson; Patricia Hirt-Minkowski; Anthony Jevnikar; S Joseph Kim; Greg Knoll; David N Rush; Chris Wiebe; Peter Nickerson
Journal:  BMJ Open       Date:  2019-04-11       Impact factor: 2.692

4.  Technical Considerations and Confounders for Urine CXCL10 Chemokine Measurement.

Authors:  Joelle Handschin; Patricia Hirt-Minkowski; Gideon Hönger; Sandra Mitrovic; Spasenija Savic Prince; Julie Ho; Peter Nickerson; Stefan Schaub
Journal:  Transplant Direct       Date:  2019-12-24

5.  Urinary Biomarkers for Diagnosis and Prediction of Acute Kidney Allograft Rejection: A Systematic Review.

Authors:  Francesco Guzzi; Luigi Cirillo; Elisa Buti; Francesca Becherucci; Carmela Errichiello; Rosa Maria Roperto; James P Hunter; Paola Romagnani
Journal:  Int J Mol Sci       Date:  2020-09-19       Impact factor: 5.923

  5 in total

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