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Induction Therapy with Low-Dose Rituximab Could Be a Risk Factor of BKV Associated Nephropathy in Kidney Transplant Recipients

R. Murakami,1 D. Nagawa,1 M. Nakata,1 I. Narita,1 T. Fujita,1 M. Shimada,1 N. Nakamura,1 H. Tomita,1 S. Hatakeyama,2 T. Yoneyama,2 Y. Hashimoto,2 T. Koie,2 C. Ohyama.2

1Nephrology, Hirosaki University, Hirosaki, Japan
2Urology, Hirosaki University, Hirosaki, Japan.

Meeting: 2018 American Transplant Congress

Abstract number: C184

Keywords: Kidney transplantation, Polyma virus, Risk factors

Session Information

Session Name: Poster Session C: Kidney: Polyoma

Session Type: Poster Session

Date: Monday, June 4, 2018

Session Time: 6:00pm-7:00pm

 Presentation Time: 6:00pm-7:00pm

Location: Hall 4EF

Background.

In kidney transplant recipients, BK polyoma virus (BKV) infection is common and serious complication that could lead to graft loss. Previous studies reported that 30-40% of kidney transplant recipients develop BK viruria, 10-20% develop BK viremia and 2-5% develop BKV associated nephropathy (BKVN). Rituximab is reported as a risk factor for BKV infection and BKVN. In our center, we use low-dose, 100mg/body of rituximab, instead of normal dose, 375mg/m2, and assessed the risk of BKVN in kidney transplant recipients at our center.

Patients and Methods.

This retrospective single-center study includes 78 patients who received living donor kidney transplantation from June 2006 to November 2016. We used low-dose rituximab (100mg/body) as an induction therapy to ABO incompatible and/or flow cytometric crossmatch positive recipients. The screening of BKV infection was performed by quantitative polymerase chain reaction test in urine and/or blood. In patients with BKV infection, BKVN was diagnosed by histological analysis including positive staining of SV-40.

Results.

Eleven patients (14.1%) developed BKVN in the early period after kidney transplantation (median, 5 months). The risk factors of BKVN were higher recipient age at transplantation (P<0.05), impaired glucose tolerance (P<0.05) and induction therapy with rituximab (P<0.05). Among the 40 patients (51.3%) who received low-dose rituximab, 13 (16.7%) developed BKV infection and 9 patients (11.5%) developed BKVN.

Conclusions.

Induction therapy using rituximab, which ABO incompatible living donor kidney transplant recipients often received in Japan, could be a risk factor for BKVN even when used in low dose.

CITATION INFORMATION: Murakami R., Nagawa D., Nakata M., Narita I., Fujita T., Shimada M., Nakamura N., Tomita H., Hatakeyama S., Yoneyama T., Hashimoto Y., Koie T., Ohyama C. Induction Therapy with Low-Dose Rituximab Could Be a Risk Factor of BKV Associated Nephropathy in Kidney Transplant Recipients Am J Transplant. 2017;17 (suppl 3).

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To cite this abstract in AMA style:

Murakami R, Nagawa D, Nakata M, Narita I, Fujita T, Shimada M, Nakamura N, Tomita H, Hatakeyama S, Yoneyama T, Hashimoto Y, Koie T, Ohyama C. Induction Therapy with Low-Dose Rituximab Could Be a Risk Factor of BKV Associated Nephropathy in Kidney Transplant Recipients [abstract]. https://atcmeetingabstracts.com/abstract/induction-therapy-with-low-dose-rituximab-could-be-a-risk-factor-of-bkv-associated-nephropathy-in-kidney-transplant-recipients/. Accessed May 16, 2025.

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