scholarly journals Conversion from tacrolimus to belatacept improves renal function in kidney transplant patients with chronic vascular lesions in allograft biopsy

2018 ◽  
Vol 12 (4) ◽  
pp. 586-591 ◽  
Author(s):  
María José Pérez-Sáez ◽  
Bryant Yu ◽  
Audrey Uffing ◽  
Naoka Murakami ◽  
Thiago J Borges ◽  
...  

AbstractBackgroundConversion from tacrolimus to belatacept has been shown to be beneficial for an increasing number of kidney transplant (KT) patients. Predicting factors for favorable outcomes are still unknown. We aimed to investigate whether histological vascular lesions at the time of conversion might correlate with greater improvement in renal function post-conversion.MethodsThe study was conducted on a retrospective cohort of 34 KT patients converted from tacrolimus to belatacept. All patients underwent an allograft biopsy prior to conversion. We analyzed the evolution of the estimated glomerular filtration rate (eGFR) at 3 and 12 months after conversion.ResultsMedian time to conversion was 6 (2–37.2) months post-transplant. About 52.9% of patients had moderate-to-severe chronic vascular lesions (cv2–3). We observed an increase in eGFR in the whole cohort from 35.4 to 41 mL/min/1.73 m2 at 3 months (P = 0.032) and 43.7 at 12 months (P = 0.013). Nine patients experienced acute rejection post-conversion, with one graft loss observed beyond the first year after conversion. Patients with cv2–3 had significant improvement in eGFR at 12 months (+8.6 mL/min/1.73 m2; 31.6 to 40.2 mL/min/1.73 m2; P = 0.047) compared with those without these lesions (+6.8 mL/min/1.73 m2; 40.9 to 47.7 mL/min/1.73 m2; P = 0.148).ConclusionsConversion from tacrolimus to belatacept has a beneficial effect in terms of renal function in KT patients. This benefit might be more significant in patients with cv in the biopsy.

2004 ◽  
Vol 36 (1) ◽  
pp. 99-101 ◽  
Author(s):  
S.H Akbas ◽  
A Yavuz ◽  
M Tuncer ◽  
C Ruhi ◽  
A Gurkan ◽  
...  

Clinics ◽  
2012 ◽  
Vol 67 (12) ◽  
pp. 1365-1371 ◽  
Author(s):  
DS Silva ◽  
ES Andrade ◽  
RM Elias ◽  
E David-Neto ◽  
WC Nahas ◽  
...  

2009 ◽  
Vol 88 (9) ◽  
pp. 1101-1108 ◽  
Author(s):  
Amado Andrés ◽  
Klemens Budde ◽  
Pierre-Alain Clavien ◽  
Thomas Becker ◽  
Michèle Kessler ◽  
...  

2012 ◽  
Vol 12 (9) ◽  
pp. 2446-2456 ◽  
Author(s):  
F. Vincenti ◽  
H. Tedesco Silva ◽  
S. Busque ◽  
P. O’Connell ◽  
J. Friedewald ◽  
...  

2020 ◽  
Vol 35 (Supplement_3) ◽  
Author(s):  
Orsolya Cseprekal ◽  
Adrienn Marton ◽  
Sara Molnar ◽  
Attila Patonai ◽  
Attila Fintha ◽  
...  

Abstract Background and Aims Pretransplant or de novo donor specific antibodies (DSA) may lead to active or chronic active antibody mediated rejection (a and cABMR) as leading cause of graft loss after kidney transplantation. There is no treatment protocol approved for ABMR. Anti Il-6 tocilizumab (TCZ), inhibitor of DSA production, is a potential approach to stabilize kidney allograft function, however, evidence based results are not available. In our retrospective case series analysis, we assessed the changes in DSA and eGFR during and at the end of treatment with TCZ. Method In our single center case series analysis, 10 kidney transplant patients with biopsy proven ABMR (aABMR 6, cABMR 4, age 43±10.5ys, 6 males, time since transplantation 18(2-119)months, 7 first transplant, serum creatinine 224±80 umol/L at baseline) were studied between January 2017 – June 2019. Total plasma exchange (PE) (5x) was followed by TCZ (8 mg/kg, 1x monthly for 6 months) in case of a and cABMR. Intravenous immunoglobulin (IVIG, 1gr/kg) was added in case of aABMR. Routine laboratory parameters and DSA were reported retrospectively. Results 6 aABMR patients completed the treatment protocol. Class I DSA decreased significantly (MFI 4457(635-14084) vs. 877(595-5678); p=0.007), but Class II DSA remained the same during the treatment (MFI 4725 (586-17615) vs. 8097 (671-14636) p=NS). eGFR of aABMR patients and 1 cABMR patient were stabilized. 3 cABMR patients returned to dialysis. Reversible elevation of liver transaminases were detected in three patients. There was no any serious adverse event recorded. Conclusion The opportunely timed TCZ seems to be effective in reducing Class I DSA and stabilize graft function in patients with aABMR. Further studies are needed to prove the long-term efficacy and the exact role of TCZ in cABMR among kidney transplant patients.


2014 ◽  
Vol 28 (1) ◽  
pp. 115-123 ◽  
Author(s):  
Klemens Budde ◽  
Claudia Sommerer ◽  
Thomas Rath ◽  
Petra Reinke ◽  
Hermann Haller ◽  
...  

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