| Literature DB >> 31167967 |
Weijia Zhang1, Zhengzi Yi1, Chengguo Wei1, Karen L Keung2, Zeguo Sun1, Caixia Xi1, Christopher Woytovich1, Samira Farouk1, Lorenzo Gallon3, Madhav C Menon1, Ciara Magee4, Nader Najafian4, Milagros D Samaniego5, Arjang Djamali6, Stephen I Alexander2, Ivy A Rosales7, Rex Neal Smith7, Philip J O'Connell2, Robert Colvin7, Paolo Cravedi1, Barbara Murphy1.
Abstract
Commonly available clinical parameters fail to predict early acute cellular rejection (EAR, occurring within 6 months after transplant), a major risk factor for graft loss after kidney transplantation. We performed whole-blood RNA sequencing at the time of transplant in 235 kidney transplant recipients enrolled in a prospective cohort study (Genomics of Chronic Allograft Rejection [GoCAR]) and evaluated the relationship of pretransplant transcriptomic profiles with EAR. EAR was associated with downregulation of NK and CD8+ T cell gene signatures in pretransplant blood. We identified a 23-gene set that predicted EAR in the discovery (n = 81, and AUC = 0.80) and validation (n = 74, and AUC = 0.74) sets. Exclusion of recipients with 5 or 6 HLA donor mismatches increased the AUC to 0.89. The risk score derived from the gene set was also significantly associated with acute cellular rejection after 6 months, antibody-mediated rejection and/or de novo donor-specific antibodies, and graft loss in a cohort of 154 patients, combining the validation set and additional GoCAR patients with surveillance biopsies between 6 and 24 months (n = 80) posttransplant. This 23-gene set is a potentially important new tool for determination of the recipient's immunological risk before kidney transplantation, and facilitation of an individualized approach to immunosuppressive therapy.Entities:
Keywords: Expression profiling; NK cells; Nephrology; Organ transplantation; Transplantation
Year: 2019 PMID: 31167967 PMCID: PMC6629121 DOI: 10.1172/jci.insight.127543
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708