Clinical Significance of Isolated V1 Arteritis in Renal Transplantation

Transplant Proc. 2021 Jun;53(5):1570-1575. doi: 10.1016/j.transproceed.2021.03.027. Epub 2021 May 13.

Abstract

Background: The presence of intimal arteritis (v) in renal allograft biopsy specimens establishes the presence of acute T-cell mediated rejection (TCMR), Grade IIa-III, according to the Banff classification of rejection. The clinical significance of isolated v1 lesions (v1), characterized by arteritis alone, compared with lesions of arteritis with tubulointerstitial inflammation (i-t-v) has been controversial.

Methods: We performed a retrospective review of 280 patients undergoing renal transplantation between 2005 and 2015 who received a "for cause" transplant biopsy using the Banff 2013 classification. Patients with TCMR grade IIa (n = 83) were subdivided into groups with isolated v1 arteritis and i-t-v. Pre- and postoperative renal function, graft survival, and overall survival were evaluated in all patients.

Results: Donor and recipient demographics were similar between groups. One month following treatment of rejection, patients with v1 disease had superior recovery of glomerular filtration rate vs patients with i-t-v (P < .002). At a median follow-up of 41 months from transplant, death-censored graft survival was 92% vs 79% (P = .04), and overall survival was 98% vs 79% (P < .004) in the isolated v1 and i-t-v groups, respectively.

Conclusion: Despite having identical Banff classification of TCMR IIa, our results indicate that graft survival in patients with isolated v1 rejection is superior to those with i-t-v. Following corroboration with data from other centers, modification of the Banff classification scheme should be considered.

Publication types

  • Evaluation Study

MeSH terms

  • Adult
  • Arteritis / immunology*
  • Biopsy
  • Glomerular Filtration Rate
  • Graft Rejection / immunology*
  • Graft Survival / immunology
  • Humans
  • Kidney / blood supply
  • Kidney Transplantation / adverse effects*
  • Male
  • Middle Aged
  • Nephritis, Interstitial / immunology*
  • Postoperative Complications / immunology*
  • Retrospective Studies
  • T-Lymphocytes / immunology
  • Transplants / blood supply