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Treatment and Outcomes of Simultaneous Acute Rejection and Polyomavirus Allograft Nephropathy.

T. Sparkes, S. Hammad, C. Drachenberg, A. Haririan.

University of Maryland, Baltimore, MD

Meeting: 2017 American Transplant Congress

Abstract number: A224

Keywords: Kidney transplantation, Polyma virus, Rejection

Session Information

Session Name: Poster Session A: Kidney: Polyoma

Session Type: Poster Session

Date: Saturday, April 29, 2017

Session Time: 5:30pm-7:30pm

 Presentation Time: 5:30pm-7:30pm

Location: Hall D1

Background: Reduction of immunosuppression for polyomavirus allograft nephropathy (PVAN) is associated with risk of acute rejection (AR), and in uncommon cases both are present together at diagnosis. Treatment of AR in the setting of PVAN is challenging, and there is limited data in this regard. We sought to examine treatment and graft outcomes after concurrent pathology.

Methods: Renal transplant recipients between 2010-2016 with biopsy-proven PVAN+AR were included.

Results: In the study period, 18 cases of simultaneous PVAN+AR were identified. Select characteristics and treatment details are outlined in the table. All patients received lymphocyte-depleting induction therapy. Simultaneous PVAN+AR was preceded by PVAN alone in 8 patients (44%), and by AR alone in 2 patients (11%). For PVAN+ACR, the rejection grade was 1B or greater in 8 (67%) of patients. After AR treatment, all patients had maintenance IS changes, the most common being reduction of CNI goal (61%). Graft failure occurred in 6 (33%), all of which occurred as sequela of the concurrent pathology; 2 patients have undergone re-transplant.

Characteristic n=18
Age at Transplant (years), mean±SD 52±10
Male, n (%) 15 (83)
Ethnicity, n (%)

African American

Caucasian

Other

9 (50)

6 (33)

3 (17)

Transplant Type, n (%)

LD

DD

10 (56)

8 (44)

Time from Transplant to PVAN+AR in Days, median (range) 120 (73-974)
Tacrolimus Level at Biopsy, mean±SD 5.1±2.9
Rejection Type, n (%)

ACR

AMR

Mixed

12 (67)

4 (22)

2 (11)

Initial Rejection Treatment, n (%)

Steroids+IVIg

Steroids

rATG

IVIg

Steroids+PP+IVIg

7 (39)

6 (33)

2 (11)

2 (11)

1 (6)

Maintenance IS Changes Post-Biopsy, n (%)

Reduction in tacrolimus/belatacept dose

Reduction in MMF dose

Reduction in steroid dose

11 (61)

6 (33)

1 (6)

Ongoing BPAR after Initial Treatment, n (%) 11 (61)
Graft Loss 6 (33)
Time to Graft Loss from Initial Biopsy in Days, median (range) 389 (113-786)
Mortality, n (%) 2 (11)

Conclusions: These data reinforce the precarious balance between rejection and infection in the renal transplant population. Almost 50% of the patients with PVAN+AR experienced PVAN alone prior to the development of simultaneous pathology, which may be attributed to aggressive IS minimization upon presentation of PVAN. Simultaneous pathology can result in rapid graft loss; therefore this population warrants close follow-up.

CITATION INFORMATION: Sparkes T, Hammad S, Drachenberg C, Haririan A. Treatment and Outcomes of Simultaneous Acute Rejection and Polyomavirus Allograft Nephropathy. Am J Transplant. 2017;17 (suppl 3).

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To cite this abstract in AMA style:

Sparkes T, Hammad S, Drachenberg C, Haririan A. Treatment and Outcomes of Simultaneous Acute Rejection and Polyomavirus Allograft Nephropathy. [abstract]. Am J Transplant. 2017; 17 (suppl 3). https://atcmeetingabstracts.com/abstract/treatment-and-outcomes-of-simultaneous-acute-rejection-and-polyomavirus-allograft-nephropathy/. Accessed May 13, 2025.

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