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Intragraft gene expression in native kidney BK virus nephropathy versus T cell–mediated rejection: Prospects for molecular diagnosis and risk prediction
Author(s) -
Adam Benjamin A.,
Kikic Zeljko,
Wagner Siegfried,
Bouatou Yassine,
Gueguen Juliette,
Drieux Fanny,
Reid Graeme,
Du Katie,
Bräsen Jan H.,
D'Agati Vivette D.,
Drachenberg Cinthia B.,
Farkash Evan A.,
Brad Farris Alton,
Geldenhuys Laurette,
Loupy Alexandre,
Nickeleit Volker,
Rabant Marion,
Randhawa Parmjeet,
Regele Heinz,
Mengel Michael
Publication year - 2020
Publication title -
american journal of transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.89
H-Index - 188
eISSN - 1600-6143
pISSN - 1600-6135
DOI - 10.1111/ajt.15980
Subject(s) - medicine , polyomavirus infections , bk virus , cohort , immunosuppression , nephropathy , immunology , biopsy , gene expression , gene , kidney , kidney transplantation , biology , endocrinology , genetics , diabetes mellitus
Novel tools are needed to improve diagnostic accuracy and risk prediction in BK virus nephropathy (BKVN). We assessed the utility of intragraft gene expression testing for these purposes. Eight hundred genes were measured in 110 archival samples, including a discovery cohort of native kidney BKVN (n = 5) vs pure T cell–mediated rejection (TCMR; n = 10). Five polyomavirus genes and seven immune‐related genes (five associated with BKVN and two associated with TCMR) were significantly differentially expressed between these entities (FDR < 0.05). These three sets of genes were further evaluated in samples representing a spectrum of BK infection (n = 25), followed by a multicenter validation cohort of allograft BKVN (n = 60) vs TCMR (n = 10). Polyomavirus 5‐gene set expression reliably distinguished BKVN from TCMR (validation cohort AUC = 0.992), but the immune gene sets demonstrated suboptimal diagnostic performance (AUC ≤ 0.720). Within the validation cohort, no significant differences in index biopsy gene expression were identified between BKVN patients demonstrating resolution (n = 35), persistent infection (n = 14) or de novo rejection (n = 11) 6 months following a standardized reduction in immunosuppression. These results suggest that, while intragraft polyomavirus gene expression may be useful as an ancillary diagnostic for BKVN, assessment for concurrent TCMR and prediction of clinical outcome may not be feasible with current molecular tools.