Successful Treatment of Plasma Cell-Rich Acute Rejection Using Bortezomib: A Case Report

Plasma cell-rich acute rejection (PCAR), a relatively rare subtype of acute allograft rejection, is usually associated with a significantly lower treatment response rate and a higher graft failure rate. PCAR is characterized by the presence of more than 10% of plasma cells out of all graft infiltrat...

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Main Authors: Sara Hashemi, Reut Hod-Dvorai, Rebecca Tong, Liye Suo
Format: Article
Language:English
Published: Wiley 2024-01-01
Series:Case Reports in Transplantation
Online Access:http://dx.doi.org/10.1155/2024/9226321
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author Sara Hashemi
Reut Hod-Dvorai
Rebecca Tong
Liye Suo
author_facet Sara Hashemi
Reut Hod-Dvorai
Rebecca Tong
Liye Suo
author_sort Sara Hashemi
collection DOAJ
description Plasma cell-rich acute rejection (PCAR), a relatively rare subtype of acute allograft rejection, is usually associated with a significantly lower treatment response rate and a higher graft failure rate. PCAR is characterized by the presence of more than 10% of plasma cells out of all graft infiltrating cells, with approximately 40%–60% of PCAR resulting in graft failure within a year. Currently, there is no gold standard for the effective treatment of PCAR. This case report demonstrates the potential treatment effect of bortezomib in PCAR. A 37-year-old woman with reflux nephropathy received a kidney transplant from a brain-dead kidney donor. The patient presented with an acute kidney injury with a serum creatinine level over 4 mg/dL 4 months after the surgery. The allograft biopsy showed acute T cell–mediated rejection (TCMR), Grade IIA, plasma cell-rich variant. There were diffuse polyclonal plasma cells infiltrating the renal parenchyma with marked tubulitis and focal endarteritis. She received a methylprednisolone pulse of 500 mg daily x3, followed by thymoglobulin (rATG) at 4.2 mg/kg. However, a repeated biopsy after 2 months showed persistent plasma cells infiltrate with increased interstitial fibrosis with tubular atrophy. Then, the patient was given one cycle of bortezomib with a total of four subcutaneous injections and continued immunosuppressants of tacrolimus, mycophenolate mofetil, and prednisone. Following the treatment, the patient’s serum creatinine level trended down to 2 mg/dL, and a second repeat biopsy after 4 months showed a significant treatment effect with complete resolution of interstitial inflammation and decreased chronicity. Bortezomib is a proteasome inhibitor that prevents cell proliferation by inducing apoptosis in plasma cells and has shown great promise as a therapeutic agent for multiple myeloma. Our case suggests that bortezomib can also be used as a potential therapeutic intervention for patients with PCAR.
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spelling doaj-art-a959a024102246dda5be4b36f97b9b442025-02-03T11:55:21ZengWileyCase Reports in Transplantation2090-69512024-01-01202410.1155/2024/9226321Successful Treatment of Plasma Cell-Rich Acute Rejection Using Bortezomib: A Case ReportSara Hashemi0Reut Hod-Dvorai1Rebecca Tong2Liye Suo3Division of Nephrology and TransplantationDepartment of PathologyDepartment of PathologyDepartment of PathologyPlasma cell-rich acute rejection (PCAR), a relatively rare subtype of acute allograft rejection, is usually associated with a significantly lower treatment response rate and a higher graft failure rate. PCAR is characterized by the presence of more than 10% of plasma cells out of all graft infiltrating cells, with approximately 40%–60% of PCAR resulting in graft failure within a year. Currently, there is no gold standard for the effective treatment of PCAR. This case report demonstrates the potential treatment effect of bortezomib in PCAR. A 37-year-old woman with reflux nephropathy received a kidney transplant from a brain-dead kidney donor. The patient presented with an acute kidney injury with a serum creatinine level over 4 mg/dL 4 months after the surgery. The allograft biopsy showed acute T cell–mediated rejection (TCMR), Grade IIA, plasma cell-rich variant. There were diffuse polyclonal plasma cells infiltrating the renal parenchyma with marked tubulitis and focal endarteritis. She received a methylprednisolone pulse of 500 mg daily x3, followed by thymoglobulin (rATG) at 4.2 mg/kg. However, a repeated biopsy after 2 months showed persistent plasma cells infiltrate with increased interstitial fibrosis with tubular atrophy. Then, the patient was given one cycle of bortezomib with a total of four subcutaneous injections and continued immunosuppressants of tacrolimus, mycophenolate mofetil, and prednisone. Following the treatment, the patient’s serum creatinine level trended down to 2 mg/dL, and a second repeat biopsy after 4 months showed a significant treatment effect with complete resolution of interstitial inflammation and decreased chronicity. Bortezomib is a proteasome inhibitor that prevents cell proliferation by inducing apoptosis in plasma cells and has shown great promise as a therapeutic agent for multiple myeloma. Our case suggests that bortezomib can also be used as a potential therapeutic intervention for patients with PCAR.http://dx.doi.org/10.1155/2024/9226321
spellingShingle Sara Hashemi
Reut Hod-Dvorai
Rebecca Tong
Liye Suo
Successful Treatment of Plasma Cell-Rich Acute Rejection Using Bortezomib: A Case Report
Case Reports in Transplantation
title Successful Treatment of Plasma Cell-Rich Acute Rejection Using Bortezomib: A Case Report
title_full Successful Treatment of Plasma Cell-Rich Acute Rejection Using Bortezomib: A Case Report
title_fullStr Successful Treatment of Plasma Cell-Rich Acute Rejection Using Bortezomib: A Case Report
title_full_unstemmed Successful Treatment of Plasma Cell-Rich Acute Rejection Using Bortezomib: A Case Report
title_short Successful Treatment of Plasma Cell-Rich Acute Rejection Using Bortezomib: A Case Report
title_sort successful treatment of plasma cell rich acute rejection using bortezomib a case report
url http://dx.doi.org/10.1155/2024/9226321
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AT rebeccatong successfultreatmentofplasmacellrichacuterejectionusingbortezomibacasereport
AT liyesuo successfultreatmentofplasmacellrichacuterejectionusingbortezomibacasereport