Recommended Treatment for Antibody-mediated Rejection After Kidney Transplantation: The 2019 Expert Consensus From the Transplantion Society Working Group.

Journal Article (Journal Article;Review)

With the development of modern solid-phase assays to detect anti-HLA antibodies and a more precise histological classification, the diagnosis of antibody-mediated rejection (AMR) has become more common and is a major cause of kidney graft loss. Currently, there are no approved therapies and treatment guidelines are based on low-level evidence. The number of prospective randomized trials for the treatment of AMR is small, and the lack of an accepted common standard for care has been an impediment to the development of new therapies. To help alleviate this, The Transplantation Society convened a meeting of international experts to develop a consensus as to what is appropriate treatment for active and chronic active AMR. The aim was to reach a consensus for standard of care treatment against which new therapies could be evaluated. At the meeting, the underlying biology of AMR, the criteria for diagnosis, the clinical phenotypes, and outcomes were discussed. The evidence for different treatments was reviewed, and a consensus for what is acceptable standard of care for the treatment of active and chronic active AMR was presented. While it was agreed that the aims of treatment are to preserve renal function, reduce histological injury, and reduce the titer of donor-specific antibody, there was no conclusive evidence to support any specific therapy. As a result, the treatment recommendations are largely based on expert opinion. It is acknowledged that properly conducted and powered clinical trials of biologically plausible agents are urgently needed to improve patient outcomes.

Full Text

Duke Authors

Cited Authors

  • Schinstock, CA; Mannon, RB; Budde, K; Chong, AS; Haas, M; Knechtle, S; Lefaucheur, C; Montgomery, RA; Nickerson, P; Tullius, SG; Ahn, C; Askar, M; Crespo, M; Chadban, SJ; Feng, S; Jordan, SC; Man, K; Mengel, M; Morris, RE; O'Doherty, I; Ozdemir, BH; Seron, D; Tambur, AR; Tanabe, K; Taupin, J-L; O'Connell, PJ

Published Date

  • May 2020

Published In

Volume / Issue

  • 104 / 5

Start / End Page

  • 911 - 922

PubMed ID

  • 31895348

Pubmed Central ID

  • PMC7176344

Electronic International Standard Serial Number (EISSN)

  • 1534-6080

Digital Object Identifier (DOI)

  • 10.1097/TP.0000000000003095


  • eng

Conference Location

  • United States