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Pretransplant transcriptomic signature in peripheral blood predicts early acute rejection
Weijia Zhang, Zhengzi Yi, Chengguo Wei, Karen L. Keung, Zeguo Sun, Caixia Xi, Christopher Woytovich, Samira Farouk, Lorenzo Gallon, Madhav C. Menon, Ciara Magee, Nader Najafian, Milagros D. Samaniego, Arjang Djamali, Stephen I. Alexander, Ivy A. Rosales, Rex Neal Smith, Philip J. O’Connell, Robert Colvin, Paolo Cravedi, Barbara Murphy
Weijia Zhang, Zhengzi Yi, Chengguo Wei, Karen L. Keung, Zeguo Sun, Caixia Xi, Christopher Woytovich, Samira Farouk, Lorenzo Gallon, Madhav C. Menon, Ciara Magee, Nader Najafian, Milagros D. Samaniego, Arjang Djamali, Stephen I. Alexander, Ivy A. Rosales, Rex Neal Smith, Philip J. O’Connell, Robert Colvin, Paolo Cravedi, Barbara Murphy
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Research Article Nephrology Transplantation

Pretransplant transcriptomic signature in peripheral blood predicts early acute rejection

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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.

Authors

Weijia Zhang, Zhengzi Yi, Chengguo Wei, Karen L. Keung, Zeguo Sun, Caixia Xi, Christopher Woytovich, Samira Farouk, Lorenzo Gallon, Madhav C. Menon, Ciara Magee, Nader Najafian, Milagros D. Samaniego, Arjang Djamali, Stephen I. Alexander, Ivy A. Rosales, Rex Neal Smith, Philip J. O’Connell, Robert Colvin, Paolo Cravedi, Barbara Murphy

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Figure 2

Pretransplant whole-blood transcriptomic signatures of the patients with or without EAR.

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Pretransplant whole-blood transcriptomic signatures of the patients with...
(A) The volcano plot of differentially expressed genes (DEGs) between the recipients who developed or did not develop EAR. The x axis depicts the log2 ratio of gene expression, and the y axis depicts the –log10 of limma P test (ref. 50). The top upregulated or downregulated genes are labeled with boxes. (B) The bar charts of enriched canonical pathways by enrichment analysis on DEGs from multiple pathway databases (indicated in parentheses). The bar represents –log10 P value of enrichment significance of gene pathways by Fisher’s exact test; the lengths of red and green bars represent the percentage of upregulated and downregulated genes, respectively. (C) The violin plot of the distribution of pretransplant serum IL-12p40 expression between those recipients who developed EAR (red bar) and those who did not (blue bar). (D) Core co-regulation modules identified by Markov Cluster Algorithm from the correlation matrix of DEGs in the recipients with EAR after transplant. The red and green nodes indicate the upregulated and downregulated genes, respectively. (E) The bar charts of enriched immune cell types for upregulated (purple bars) and downregulated (green bars) genes based on immune cell–specific genes identified from ImmGen database. The x axis depicts –log10 P value of enrichment significance of immune cell types. gd, gamma delta.

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ISSN 2379-3708

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