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Use of HCV Ab+/NAT- Donors in HCV Naïve Renal Transplant Recipients

A. Dao,1 M. Cuffy,1 T. Kaiser,1 A. Loethen,1 J. Cafardi,2 A. Shields,2 M. Cardi,2 R. Alloway,1 A. Govil,1 K. Sherman,1 S. Shah,1 E. Woodle.1

1Univeristy of Cincinnati Medical Center, Cincinnati, OH
2The Christ Hospital, Cincinnati, OH.

Meeting: 2018 American Transplant Congress

Abstract number: 111

Keywords: Donors, Hepatitis C, Kidney transplantation, marginal

Session Information

Session Name: Concurrent Session: Kidney Donor Selection / Management Issues - 1

Session Type: Concurrent Session

Date: Sunday, June 3, 2018

Session Time: 4:30pm-6:00pm

 Presentation Time: 4:42pm-4:54pm

Location: Room 6E

The continued organ shortage in renal transplantation (RT) has stimulated use of organs from increased-risk donors to expand the donor pool. The rate of denovo Hepatitis C (HCV) infection from the use of HCV antibody (HCVAb) positive and HCV nucleic acid test (HCVNAT) negative kidney allografts is unknown. Study aim was to prospectively analyze RT outcomes from HCVAb+/NAT- donors to HCV naïve recipients under T-cell depleting early steroid withdrawal (ESW) immunosuppression (IS).

Methods: HCV naïve RT recipients transplanted with a HCVAb+/NAT- allograft (Dec 2015-Nov 2017) were prospectively reviewed. Donor/recipient characteristics, IS strategies, and clinical outcomes (allograft function, graft/patient survival, and de novo HCV infection) were collected. Per center monitoring guidelines, recipients underwent HCV PCR testing (Roche COBAS® Ampliprep TNAI/ TaqMan® 48 RUO Assay; limit of detection 15 IU/ml) at 3 months post-RT or sooner if clinically indicated.

Results: Kidneys from 32 HCVAb+/NAT- donors were transplanted to 43 HCVAb- recipients at 2 centers. Analysis includes 25 recipients (allografts from 22 donors) with 3-month follow-up. Table 1 summarizes donor/recipient characteristics. HCVNAT testing within the eclipse period occurred in 95% of donors. IS received by 96% included anti-thymocyte globulin, tacrolimus, and 7-day ESW. Rate of de novo HCV infection is 4% (1/25). HCV viremia at 92 days post-RT in a 61 year old male transplanted for IgA nephropathy; initiation of anti-viral therapy (glecaprevir/pibrentasvir for 12 weeks) is underway. One death at 261 days post-RT due to unknown causes (autopsy not performed) was determined not related to HCV or donor factors. Table 2 summarizes clinical outcomes.

Conclusion: This represents the largest, prospective series of HCVAb+/NAT- donors transplanted to HCV naive recipients with a 4% rate of HCV transmission under T-cell depleting ESW IS. Our experience demonstrates an effective strategy to expand the donor pool, decrease waitlist times, and decrease discard rates of HCV positive kidneys.

CITATION INFORMATION: Dao A., Cuffy M., Kaiser T., Loethen A., Cafardi J., Shields A., Cardi M., Alloway R., Govil A., Sherman K., Shah S., Woodle E. Use of HCV Ab+/NAT- Donors in HCV Naïve Renal Transplant Recipients Am J Transplant. 2017;17 (suppl 3).

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To cite this abstract in AMA style:

Dao A, Cuffy M, Kaiser T, Loethen A, Cafardi J, Shields A, Cardi M, Alloway R, Govil A, Sherman K, Shah S, Woodle E. Use of HCV Ab+/NAT- Donors in HCV Naïve Renal Transplant Recipients [abstract]. https://atcmeetingabstracts.com/abstract/use-of-hcv-ab-nat-donors-in-hcv-nave-renal-transplant-recipients/. Accessed May 9, 2025.

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