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Tocilizumab in Chronic Active Antibody-Mediated Rejection in Kidney Transplant Recipients: A Case Series

B. Boonpheng1, R. Bakthavatsalam2, C. D. Blosser1, I. C. De Castro1, I. Gimferrer3, Y. Ng1, N. Leca1

1Nephrology, University of Washington, Seattle, WA, 2Surgery, University of Washington, Seattle, WA, 3Bloodworks Northwest, Seattle, WA

Meeting: 2022 American Transplant Congress

Abstract number: 1407

Keywords: Graft survival, Kidney transplantation, Rejection, Renal function

Topic: Clinical Science » Kidney » 45 - Kidney Chronic Antibody Mediated Rejection

Session Information

Session Name: Kidney Chronic Antibody Mediated Rejection

Session Type: Poster Abstract

Date: Monday, June 6, 2022

Session Time: 7:00pm-8:00pm

 Presentation Time: 7:00pm-8:00pm

Location: Hynes Halls C & D

*Purpose: The optimal treatment for chronic active antibody-mediated rejection (ca-AMR) remains unclear. Tocilizumab (TCZ), a monoclonal antibody against IL-6, has been proposed in ca-AMR treatment to reduce the inflammation and injury without significant side effects. We reported our experience with treatment of ca-AMR with TCZ either as the first line option or as a rescue therapy.

*Methods: 10 adult kidney transplant recipients with biopsy-proven ca-AMR who were treated with TCZ (8 mg/kg IV monthly) were enrolled. Creatinine, urinary protein/creatinine ratio, donor-specific antibody (DSA) and donor-derived cell-free DNA percentage (%dd-cfDNA) and side effects were monitored at least every 3 months.

*Results: In this cohort, mean age of patients was 47 years. CA-AMR was diagnosed at a median of 8.3 years (range 1.2-19 years) post-transplant. Patient received a minimum of 3 months of TCZ. Median duration of treatment was 6.5 months (range 3-12 months). At 3 months, creatinine. DSA and %dd-cfDNA remained stable but proteinuria reduced significantly (average reduction 47% ± 31%, p=0.02). At 6 months, %dd-cfDNA reduced significantly by 66% ± 23% (p=0.01) while Cr and DSA remained unchanged (change Cr 0.01 ± 0.26, change in DSA -267 ± 3100 MFI, p>0.05). All patients had elevated dd-cfDNA≥1% and with treatment in 6/10 the dd-cfDNA decreased below the threshold of <1%. Only one patient experienced a severe infection episode during treatment (C difficile colitis). Overall no patient has lost their grafts in this cohort.

*Conclusions: In our early short-term experience, TCZ appears to reduce graft injury as seen by %dd-cfDNA and proteinuria. There was no worsening of allograft function and DSA remained unchanged. No significant side effect was observed in our cohort.

Patient Characteristics
Age (mean, SD) 47 +/- 11 years
Living donor transplant 60%
Deceased donor transplant 30%
Simultaneous  kidney-pancreas transplant 10%
Time to diagnosis from transplant 99 months (range 14-227)
Previous treatment for AMR/CA-AMR 30% (IVIG +/- Rituximab)
Positive DSA at the time of diagnosis 70%
C4d positive 70%

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To cite this abstract in AMA style:

Boonpheng B, Bakthavatsalam R, Blosser CD, Castro ICDe, Gimferrer I, Ng Y, Leca N. Tocilizumab in Chronic Active Antibody-Mediated Rejection in Kidney Transplant Recipients: A Case Series [abstract]. Am J Transplant. 2022; 22 (suppl 3). https://atcmeetingabstracts.com/abstract/tocilizumab-in-chronic-active-antibody-mediated-rejection-in-kidney-transplant-recipients-a-case-series/. Accessed May 28, 2025.

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