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CMV and BKV Infections after Kidney Transplantation: Combined Tacrolimus/everolimus Strategy Using Antithymocyte Globulin Induction

T. Jouve,1,4 R. Germi,2,4 B. Janbon,1 G. Fiard,3,4 P. Malvezzi,1 L. Rostaing.1,4

1Nephrology, Dialysis, Apheresis, Transplantation Unit, Grenoble University Hospital, Grenoble, France
2Virology Unit, Grenoble University Hospital, Grenoble, France
3Urology Unit, Grenoble University Hospital, Grenoble, France
4Medical Sciences, Grenoble University, Grenoble, France.

Meeting: 2018 American Transplant Congress

Abstract number: C92

Keywords: Cytomeglovirus, Infection, Kidney transplantation, Polyma virus

Session Information

Session Name: Poster Session C: Kidney Immunosuppression: Novel Regimens and Drug Minimization

Session Type: Poster Session

Date: Monday, June 4, 2018

Session Time: 6:00pm-7:00pm

 Presentation Time: 6:00pm-7:00pm

Location: Hall 4EF

Cytomegalovirus (CMV) and BK Virus (BKV) infections are frequent complications after kidney transplantation. A combined regimen of calcineurin inhibitor (CNI) and mTOR inhibitors (mTORi) reduces the rate of CMV and BKV infections after transplantation. We report on our experience with early tacrolimus and everolimus.

In this study, we prospectively enrolled new kidney transplant recipients at our center between july of 2016 and july of 2017. Inclusion criteria were non-sensitized, ABO compatible, first time kidney transplant recipient, age 18 or older, either recipient CMV positive, or CMV negative for both the donor and the recipient. Patients received an induction with antithymocyte globulins, steroids and tacrolimus together with everolimus from day 1 post-transplantation. Steroids were maintained over at least the first 3 months, then depending on a systematic kidney biopsy at month 3. Targeted trough levels over the first month were 5-7 [micro]g/l for tacrolimus and 4-6 [micro]g/l for everolimus, then 4-5 for tacrolimus and 5-7 for everolimus. We did not use CMV prophylaxis.

We monitored CMV and BKV blood PCR preemptively over the first 6 months, at month 0, 1, and 3 and for any suspicion of infection. We defined a viral infection as a positive PCR > 1000 (3 log) copies/ml.

We included 58 consecutive patients. Trough concentrations for tacrolimus and everolimus are represented on figure 1. The rate of CMV infections was 8/58 (13.8%), with a mean time time between transplantation and infection of 72 (min=30, max=214) days. The rate of BKV infections was 3/58 (5.1%), with a mean time between transplantation and infection of 91 (min=33, max=177) days.

Compared to a 10% rate of CMV infections reported in the literature, it seems that using tacrolimus together with everolimus is efficient in preventing CMV and BKV infections, even in antithymocytes globulines induced patients.

CITATION INFORMATION: Jouve T., Germi R., Janbon B., Fiard G., Malvezzi P., Rostaing L. CMV and BKV Infections after Kidney Transplantation: Combined Tacrolimus/everolimus Strategy Using Antithymocyte Globulin Induction Am J Transplant. 2017;17 (suppl 3).

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To cite this abstract in AMA style:

Jouve T, Germi R, Janbon B, Fiard G, Malvezzi P, Rostaing L. CMV and BKV Infections after Kidney Transplantation: Combined Tacrolimus/everolimus Strategy Using Antithymocyte Globulin Induction [abstract]. https://atcmeetingabstracts.com/abstract/cmv-and-bkv-infections-after-kidney-transplantation-combined-tacrolimus-everolimus-strategy-using-antithymocyte-globulin-induction/. Accessed May 16, 2025.

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