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Mixed Acute Rejection: Comparison of Therapeutic Results with Anti-T Cell Antibody- and Proteasome Inhibitor-Based Regimens

F. Paterno, B. Sadaka, A. Shields, R. Alloway, M. Cardi, J. Kremer, M. Cuffy, T. Diwan, E. Woodle

University of Cincinnati
The Christ Hospital

Meeting: 2013 American Transplant Congress

Abstract number: D1593

Background: Mixed acute rejection (MAR) has been defined as acute rejection consisting of both cellular and humoral components. No data exist regarding MAR treatment outcomes, nor whether T cell- or B cell-targeted therapies provide optimal results. The aim of this study is to evaluate the outcomes of different treatments of MAR in kidney transplant recipients.

Methods: MAR was defined as coexisting acute cellular- and antibody-mediated rejection. Patient groups examined included two from a prospective randomized MAR trial (Groups B and C), which were compared to an off-protocol standard of care regimen (Group A). Group A: bortezomib (BTZ) + rituximab (Ritux); Group B: BTZ + rabbit anti-thymocyte globulin (rATG); Group C: rATG + Ritux.

Results: 27 patients were included in the study. As shown in the table, all three groups had similar results in renal function, donor-specific antibodies (DSA), Banff scores. Five patients (18.5%) experienced graft loss: there was no difference among the three groups.

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To cite this abstract in AMA style:

Paterno F, Sadaka B, Shields A, Alloway R, Cardi M, Kremer J, Cuffy M, Diwan T, Woodle E. Mixed Acute Rejection: Comparison of Therapeutic Results with Anti-T Cell Antibody- and Proteasome Inhibitor-Based Regimens [abstract]. Am J Transplant. 2013; 13 (suppl 5). https://atcmeetingabstracts.com/abstract/mixed-acute-rejection-comparison-of-therapeutic-results-with-anti-t-cell-antibody-and-proteasome-inhibitor-based-regimens/. Accessed May 14, 2025.

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  A: BTZ+Ritux (n=7) B: BTZ+rATG (n=10) p-value (A vs B) C: rATG+Ritux (n=10) p-value (A vs C)
Age(yr)† 49.5 ± 14.5 41.5 ± 13.3 NS 36.5 ± 5.5 0.019
Deceased donor transplant, n (%) 3 (42.8%) 5 (50%) NS 3 (30%) NS
Female, n (%) 3 (42.8%) 4 (40.0%) NS 3 (30%) NS
Late (>6 mos) MAR, n (%) 5 (71.4%) 9 (90.0%) NS 7 (70%) NS
AA race, n (%) 2 (28.6%) 5 (50%) NS 2 (20%) NS
Time to rejection (mos)† 30.7 ± 26.6 35.4 ± 27.1 NS 31.5 ± 47.3 NS
Post-tx follow-up (mos) 15.8 ± 13.5 18.6 ± 11.7 NS 14.1 ± 13.0 NS
eGFR at baseline (ml/min/1.73m²)† 80 ± 13.5 62.3 ± 9.9 0.007 71.1 ± 23.9 NS
eGFR at rejection diagnosis (ml/min/1.73m²)† 26.8 ± 15.5 32.9 ± 17.0 NS 37.4 ± 28.3 NS
eGFR maximum post-tx (ml/min/1.73m²)† 44.9 ± 17.7 46.0 ± 17.1 NS 44.6 ± 20.3 NS
% decrease in eGFR post-tx 55.3 ± 10.44 29.2 ± 16.7 NS 32.7 ± 40.4 NS
Pre-tx iDSA level (MFI)† 11,750 ± 8202 8252 ± 4109 NS 9358 ± 6667 NS
Nadir iDSA level (MFI)† 4363 ± 5760 3175 ± 2275 NS 6392 ± 5778 NS
% reduction in nadir iDSA level (MFI)† 52.8 ± 30.4 64.7 ± 21.7 NS 50.0 ± 29.4 NS
Change in Banff scoring post-tx†          
g + ptc -0.6 ± 0.8 -0.4 ± 0.4 NS 0.1 ± 0.9 NS
i + t -1.4 ± 1.9 -1.2 ± 1.3 NS -1.3 ± 1.8 NS
c4d -0.3 ± 0.7 1.0 ± 0 NS 0 ± 0.8 NS
cg 0.1 ± 0.4 -0.2 ± 0.4 NS 0 NS
ci + ct + cv 0.6 ± 1.3 0.6 ± 3.1 NS 0.9 ± 2 NS
Graft loss, n (%)