Literature DB >> 27367750

Failure of Calcineurin Inhibitor (Tacrolimus) Weaning Randomized Trial in Long-Term Stable Kidney Transplant Recipients.

E Dugast1,2, J-P Soulillou1,2, Y Foucher3, E Papuchon1,4, P Guerif1,4, C Paul1, D Riochet5,6, M Chesneau1, A Cesbron7,8, K Renaudin1,2, J Dantal1, M Giral9,10,11,12, S Brouard1,7,13,14.   

Abstract

Long-term renal transplant outcome is limited by side effects of immunosuppressive drugs, particularly calcineurin inhibitor (CNI). We assumed that some patients selected for a "low immunological risk of rejection" could be eligible and benefit from a CNI weaning strategy. We designed a prospective, randomized, multicenter, double-blind placebo-controlled clinical study (Eudract: 2010-019574-33) to analyze the benefit-risk ratio of tacrolimus weaning on highly selected patients (≥4 years of transplantation, normal histology, stable graft function, no anti-HLA immunization). The primary endpoint was improvement of renal function. Fifty-two patients were scheduled in each treatment arm, placebo compared to the CNI maintenance arm. Only 10 patients were eligible and randomized. Five patients were assigned to the placebo arm and five were assigned to the tacrolimus maintenance arm. In the tacrolimus maintenance arm, all patients maintained stable graft function and no immunological events occurred. Contrastingly, in the placebo arm, all five patients had to reintroduce a full dose of tacrolimus since three of them presented an acute rejection episode (one humoral, one mixed, and one borderline) and two displayed anti-HLA antibodies without histological lesion (one donor-specific antibodies [DSA] and one non-DSA). Clearly, tacrolimus withdrawal must be avoided even in long-term highly selective stable kidney recipients. © Copyright 2016 The American Society of Transplantation and the American Society of Transplant Surgeons.

Entities:  

Keywords:  alloantibody; biopsy; chronic allograft nephropathy; clinical research/practice; clinical trial; immunosuppressant; immunosuppression/immune modulation; kidney transplantation/nephrology

Mesh:

Substances:

Year:  2016        PMID: 27367750     DOI: 10.1111/ajt.13946

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


  21 in total

1.  Avoidance of CNI and steroids using belatacept-Results of the Clinical Trials in Organ Transplantation 16 trial.

Authors:  Roslyn B Mannon; Brian Armstrong; Peter G Stock; Aneesh K Mehta; Alton B Farris; Natasha Watson; Yvonne Morrison; Minnie Sarwal; Tara Sigdel; Nancy Bridges; Mark Robien; Kenneth A Newell; Christian P Larsen
Journal:  Am J Transplant       Date:  2020-07-13       Impact factor: 8.086

Review 2.  Operational tolerance in kidney transplantation and associated biomarkers.

Authors:  A Massart; L Ghisdal; M Abramowicz; D Abramowicz
Journal:  Clin Exp Immunol       Date:  2017-05-29       Impact factor: 4.330

3.  Tacrolimus Variability: A Cause of Donor-Specific Anti-HLA Antibody Formation in Children.

Authors:  Gulsah Kaya Aksoy; Elif Comak; Mustafa Koyun; Halide Akbaş; Bahar Akkaya; Bülent Aydınlı; Fahri Uçar; Sema Akman
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2019-02-08       Impact factor: 2.441

4.  A composite score associated with spontaneous operational tolerance in kidney transplant recipients.

Authors:  Richard Danger; Mélanie Chesneau; Chloé Paul; Pierrick Guérif; Maxim Durand; Kenneth A Newell; Sai Kanaparthi; Laurence A Turka; Jean-Paul Soulillou; Rémi Houlgatte; Magali Giral; Gérard Ramstein; Sophie Brouard
Journal:  Kidney Int       Date:  2017-02-24       Impact factor: 10.612

5.  Distinct peripheral blood molecular signature emerges with successful tacrolimus withdrawal in kidney transplant recipients.

Authors:  Paolo Cravedi; Miguel Fribourg; Weijia Zhang; Zhengzi Yi; Elena Zaslavsky; German Nudelman; Lisa Anderson; Susan Hartzell; Sophie Brouard; Peter S Heeger
Journal:  Am J Transplant       Date:  2020-05-27       Impact factor: 8.086

Review 6.  Biomarkers of operational tolerance following kidney transplantation - The immune tolerance network studies of spontaneously tolerant kidney transplant recipients.

Authors:  Kenneth A Newell; Andrew B Adams; Laurence A Turka
Journal:  Hum Immunol       Date:  2018-02-12       Impact factor: 2.850

7.  B Cell Receptor Genes Associated With Tolerance Identify a Cohort of Immunosuppressed Patients With Improved Renal Allograft Graft Function.

Authors:  A Asare; S Kanaparthi; N Lim; D Phippard; F Vincenti; J Friedewald; M Pavlakis; E Poggio; P Heeger; R Mannon; B E Burrell; Y Morrison; N Bridges; I Sanz; A Chandraker; K A Newell; L A Turka
Journal:  Am J Transplant       Date:  2017-05-02       Impact factor: 8.086

8.  Class II Eplet Mismatch Modulates Tacrolimus Trough Levels Required to Prevent Donor-Specific Antibody Development.

Authors:  Chris Wiebe; David N Rush; Thomas E Nevins; Patricia E Birk; Tom Blydt-Hansen; Ian W Gibson; Aviva Goldberg; Julie Ho; Martin Karpinski; Denise Pochinco; Atul Sharma; Leroy Storsley; Arthur J Matas; Peter W Nickerson
Journal:  J Am Soc Nephrol       Date:  2017-07-20       Impact factor: 10.121

Review 9.  Immune monitoring as prerequisite for transplantation tolerance trials.

Authors:  K Behnam Sani; B Sawitzki
Journal:  Clin Exp Immunol       Date:  2017-06-23       Impact factor: 4.330

Review 10.  Harnessing Mechanisms of Immune Tolerance to Improve Outcomes in Solid Organ Transplantation: A Review.

Authors:  Priscila Ferreira Slepicka; Mahboubeh Yazdanifar; Alice Bertaina
Journal:  Front Immunol       Date:  2021-06-10       Impact factor: 7.561

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