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Impact of Protease Inhibitor-Based Anti-Retroviral Therapy on Tacrolimus Intrapatient Variability in HIV+ Kidney Transplant Recipients

M. H. Cooper, I. E. Dunne, S. A. Kuten, A. E. Cantwell, E. A. Graviss, D. T. Nguyen, M. J. Hobeika, A. O. Gaber

Houston Methodist Hospital, Houston, TX

Meeting: 2019 American Transplant Congress

Abstract number: B212

Keywords: HIV virus, Immunosuppression, Kidney transplantation, Rejection

Session Information

Session Name: Poster Session B: Kidney Infections

Session Type: Poster Session

Date: Sunday, June 2, 2019

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

 Presentation Time: 6:00pm-7:00pm

Location: Hall C & D

*Purpose: High tacrolimus (FK) intra-patient variability (IPV) has been associated with inferior outcomes in solid organ transplantation. HIV+ transplant recipients have been shown to experience higher rates of acute rejection, possibly due to the drug-drug interactions that exist between highly active anti-retroviral therapy (HAART) and immunosuppression regimens. In this study, we aim to determine the impact of protease inhibitor (PI)-based HAART regimens on FK variability and whether this affects overall immune outcomes.

*Methods: We performed a single-center review of HIV+ kidney transplant recipients from 2007 to 2017. Patients were divided into high or low tacrolimus trough level variability cohorts based on median % coefficient of variation [%CV = (σ/μ) x 100; σ, median; μ, mean]. Lymphocyte-depleting induction was administered to patients with the following characteristics: African American, PRA ≥20%, and/or re-transplants. All patients were discharged on tacrolimus, mycophenolate, and prednisone.

*Results: A total of 23 HIV+ kidney transplant patients were included, of which 10 were on PI-based based HAART. Baseline demographics are reported in Table 1. Median IPV at 6 months was 36%; rates of high IPV among PI-based vs. non-PI-based regimens were 60% and 38%, respectively. At 12 months, high IPV was observed in 70% PI-based compared to 31% non-PI-based patients. Overall rates of rejection were similar between groups. Of note, one patient was switched from PI to non-PI-based HAART due to an early acute rejection and another patient on PI-based HAART was switched to belatacept to avoid drug-drug interactions.

*Conclusions: Our data suggests that PI-based regimens may be associated with a higher degree of FK variability during the first year post-transplant. However, given the small sample size, we did not observe significant differences in immune outcomes between the two groups. Further studies are warranted to determine the impact of PI-based HAART on FK IPV and subsequent graft outcomes in HIV+ transplant recipients.

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To cite this abstract in AMA style:

Cooper MH, Dunne IE, Kuten SA, Cantwell AE, Graviss EA, Nguyen DT, Hobeika MJ, Gaber AO. Impact of Protease Inhibitor-Based Anti-Retroviral Therapy on Tacrolimus Intrapatient Variability in HIV+ Kidney Transplant Recipients [abstract]. Am J Transplant. 2019; 19 (suppl 3). https://atcmeetingabstracts.com/abstract/impact-of-protease-inhibitor-based-anti-retroviral-therapy-on-tacrolimus-intrapatient-variability-in-hiv-kidney-transplant-recipients/. Accessed May 8, 2025.

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