What Is The Role Of Cistanche Play in A Kidney Transplant Recipient

Acute Kidney Injury Following Chimeric Antigen Receptor T-Cell Therapy for B-Cell Lymphoma in a Kidney Transplant Recipient

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Keywords: acute kidney injury, chimeric antigen receptor, kidney transplant recipient, kidney

BACKGROUND

Anti-CD19 chimeric antigen receptor T-cell therapy is a newer and more effective therapeutic option approved for patients with relapsed/refractory acute lymphoblastic leukemia and diffuse large B-cell lymphoma. Acute kidney injury is a complication of chimeric antigen receptor T-cell therapy that can result in kidney failure. In most cases, it is thought to be related to hemodynamic changes due to cytokine release syndrome. A kidney biopsy in this clinical scenario is usually not performed. We report on a kidney transplant recipient in his 40s who developed a posttransplant lymphoproliferative disorder of B-cell origin refractory to conventional treatments and received anti-CD19 chimeric antigen receptor T-cell therapy as compassionate treatment. Beginning on day 12 after chimeric antigen receptor T-cell infusion, in the absence of clinical symptoms, a progressive decline in the estimated glomerular filtration rate of the kidney graft occurred. A subsequent allograft biopsy showed mild tubulointerstitial lymphocyte infiltrates, falling into a Banff borderline-changes category and resembling an acute immune allergic tubulointerstitial nephritis. Neither chimeric antigen receptor T cells nor lymphomatous B cells were detected within the graft cellular infiltrate, suggesting an indirect mechanism of kidney injury. Although kidney graft function partially recovered after steroid therapy, the posttransplant lymphoproliferative disorder progressed and the patient died 7 months later.

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INTRODUCTION

Posttransplant lymphoproliferative disorder represents a rare but serious complication after organ transplantation. 1 Treatment includes reduction or withdrawal of immuno-

suppression followed by rituximab with or without chemotherapy. 2,3 Transplant recipients who fail to respond or relapse after conventional treatments have a poor prognosis. 4 Chimeric antigen receptor T cells directed against CD19 surface antigen represent a recent type of autologous adoptive transfer cell therapy currently approved for the treatment of relapsed/refractory diffuse large B-cell lymphoma and other hematologic malignancies. 5-8 Apart from cytokine release syndrome and neurotoxicity, 9,10 other adverse events have been described, including acute kidney injury and electrolyte level abnormalities. 11 Recently, several solid-organ transplant recipients treated with chimeric antigen receptor T-cell therapy were reported. 12 We describe the case of a kidney transplant recipient who developed severe acute kidney injury after chimeric antigen receptor T-cell therapy. A kidney biopsy was performed, helping clarify the pathogenesis of this unique case.

CASE REPORT

A kidney transplant recipient in his 40s was diagnosed with monomorphic type B-cell posttransplant lymphoproliferative disorder approximately 18 years after transplantation; induction therapy included basiliximab. He had a large abdominal mass and supraclavicular lymphadenopathy but no additional organ involvement was detected with staging positron emission tomography-computed tomography. He was classified with Ann Arbor stage IVB disease, with an international prognostic score of 2. Histologic characterization of malignant cells showed the following: CD20+, CD79+, CD10+, bcl6+, bcl2+, p53+, c-myc+, CD3−, and CD5−. Additionally, Epstein-Barr virus-encoded small RNA and human herpesvirus-8 were negative. Fluorescence in situ hybridization was positive for BCL2 but negative for either BCL6 or c-MYC. Ki67 expression was >80%. pathogenesis of this unique case.

Immunosuppression was reduced, with tacrolimus switched to everolimus, and mycophenolate mofetil dose decreased to 50%. Four weekly infusions of rituximab were administered. Due to disease progression, he subsequently received 3 cycles of R-CHOP (rituximab, cyclophosphamide, doxorubicin hydrochloride, vincristine sulfate, and prednisone) immunochemotherapy. Everolimus was reduced to 50% and mycophenolate mofetil therapy was discontinued. Due to disease persistence, intensification treatment with 2 cycles of R-GDP (rituximab, gemcitabine, dexamethasone, and cisplatin) immunochemotherapy was administered and, with the exception of 5 mg of prednisone daily, immunosuppression was discontinued. Autologous hematopoietic stem cell transplantation consolidation was performed but relapse was observed in positron emission tomography-computed tomography performed 3 months after autologous hematopoietic stem cell transplantation. Approximately 28 months after the initial diagnosis, the patient received lymphodepletion chemotherapy with intravenous fludarabine and intravenous cyclophosphamide for 3 days, followed by chimeric antigen receptor T-cell therapy (tisagenlecleucel) infusion. The patient developed grade 3 neutropenia without significant acute complications. The baseline creatinine level was 1.5 mg/dL. On day 12 after chimeric antigen receptor T-cell infusion, serum creatinine and C-reactive protein levels began to increase, without relevant symptoms and without oliguria (Fig 1). Neither cytokine release syndrome nor immune effector cell-associated neurotoxicity syndrome was observed. All potentially nephrotoxic drugs (omeprazole and acyclovir) were stopped. Proteinuria was protein excretion of 0.4 g/d, and sediment showed mild leukocyturia with no erythrocytes. Myoglobin and creatine kinase levels were within the normal range. Polymerase chain reaction for cytomegalovirus was negative. Doppler ultrasound showed a mild increase in kidney echogenicity, with normal resistive index and no sign of obstruction. The calculated panel-reactive antibody level at the time of biopsy was 39% for the presence of alloantibodies against class II, without donor-specific antibodies.

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On day 21 after chimeric antigen receptor T-cell therapy administration, serum creatinine level had increased to 6 mg/dL and a kidney biopsy was performed; C-reactive protein level was 43 mg/dL at that time. The biopsy showed interstitial fibroadenoma with moderate mononuclear infiltrates and patchy tubular injury with epithelial thinning, coarse cytoplasmic vacuolization, and mild isolated tubulitis.

Arteriolar changes were prominent and demonstrated periodic acid–Schiff–positive hyaline deposits deep in muscle layers. Glomeruli were unremarkable. C4d and immuno-

globulins were negative on direct immunofluorescence. Immunohistochemical staining for simian virus 40 was negative. Banff classification was compatible with borderline changes not grading 1A acute cellular rejection (Fig S1). The presumptive diagnosis was acute borderline changes in the context of mild alloimmune rejection versus acute immune allergic interstitial nephritis.

We next aimed to characterize the origin of the lymphocytic infiltrate in the kidney biopsy. As shown in Fig 2, lymphocytic infiltrate was comprised exclusively of CD3+

lymphocytes, with no CD19+ cells. RNA-scope, a technique used to evaluate the expression of the gene encoding the engineered chimeric antigen receptor, did not show evidence of chimeric antigen receptor T-cell–19 infiltration in the kidney. Aiming to reduce lymphocytic infiltrates but also preserve chimeric antigen receptor T-cell function, prednisone was initiated at a dose of 1 mg/kg per day. 13 Kidney allograft function partially recovered, reaching a nadir of 3.17 mg/dL after 60 days (Fig 2), whereas proteinuria was unchanged. Prednisone dosage was progressively tapered to 10 mg per day by 40 days after the kidney biopsy. At 30 and 60 days following chimeric antigen receptor T-cell therapy, peripheral-blood CD19+ B-cell counts were undetectable. The patient died approximately 3 years after the initial posttransplant lymphoproliferative disorder diagnosis due to the progression of the malignancy.

DISCUSSION

To our knowledge, this is the first report of a kidney biopsy performed in a kidney transplant recipient treated with anti-CD19 chimeric antigen receptor T-cell therapy. The main acute treatment-related toxicity was KDIGO (Kidney Disease: Improving Global Outcomes) stage III acute kidney injury 14 that partially recovered with steroid therapy. acute kidney injury has been reported in 19% to 30% of patients undergoing chimeric antigen receptor T-cell therapy. 12,15 The occurrence of acute kidney injury after chimeric antigen receptor T-cell therapy is thought to be functional, secondary to arterial hypotension in the context of cytokine release syndrome. Nonetheless, more severe acute kidney injury episodes are likely due to the persistence of severe hemodynamic alterations leading to acute tubular necrosis, 16 but none of these studies provided data on the histopathology of the kidney injury.

Recently, a study reported that among patients with B-cell lymphoproliferative disorders and kidney lymphoma infiltration, acute kidney injury was common. 17 This observation raises the concern that chimeric antigen receptor T-cell therapy might damage the kidney by recognizing kidney tissue-resident B cells. In our case, we did not observe B-cell infiltration in the kidney on a kidney biopsy performed 3 weeks after chimeric antigen receptor T-cell therapy infusion. Importantly, no chimeric antigen receptor19 RNA was detected, thereby excluding the presence of chimeric antigen receptor T-cells in the kidney allograft at the time of the kidney biopsy. Findings observed in the graft histology could have been promoted by a chimeric antigen receptor T-cell–induced systemic inflammatory status, thus explaining the resemblance to an acute immune allergic tubulointerstitial nephritis. Alternatively, biopsy findings could reflect an alloimmune response stimulated by cognate T-cell with endogenous lymphocyte inducing an acute cellular rejection. We decided to use steroids to manage this complication, observing partial recovery of graft function that was sufficient to prevent dialysis therapy and potentially preserve chimeric antigen receptor T-cell function, as demonstrated by the absence of peripheral-blood CD19+ cells. 18 Although proton pump inhibitor use has been associated with acute kidney injury in patients treated by immune-checkpoint inhibitors 19 through a second-hit mechanism, no similar data have been reported with chimeric antigen receptor T-cell therapy, suggesting that proton pump inhibitor use was not likely the cause of acute kidney injury.

CONCLUSION

In conclusion, although there was no evidence of damage mediated by direct infiltration of chimeric antigen receptor T-cells in the kidney, our case suggests that this new therapy could generate kidney graft failure through an indirect inflammatory and/or immune-mediated mechanism, stressing the central role of the kidney biopsy to guide therapy.

REFERENCES

The source is from Edoardo Melilli etc, al on Kidney Med. 3(4):665-668. Published online May 28, 2021.