Outcome of Kidney Transplantations Performed With Preformed Donor‐Specific Antibodies of Unknown Etiology

The detection of preformed donor‐specific alloantibodies (DSA) with multiplex‐bead arrays has led to the common observation that individuals without a history of pregnancy, transfusion or transplantation can have circulating anti‐HLA antibodies of unknown etiology. We retrospectively analyzed the ri...

Full description

Saved in:

Bibliographic Details
Published in:	American journal of transplantation 2014-01, Vol.14 (1), p.193-201
Main Authors:	Sicard, A., Amrouche, L., Suberbielle, C., Carmagnat, M., Candon, S., Thervet, E., Delahousse, M., Legendre, C., Chatenoud, L., Snanoudj, R.
Format:	Article
Language:	eng
Subjects:	Adult antibody‐mediated rejection Anti‐HLA antibodies Biological and medical sciences desensitization protocol Desensitization, Immunologic donor‐specific antibodies Graft Rejection - immunology Humans Isoantibodies - immunology Kidney Transplantation Male Medical sciences Middle Aged Retrospective Studies Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the urinary system Tissue Donors Treatment Outcome
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Description
Summary:	The detection of preformed donor‐specific alloantibodies (DSA) with multiplex‐bead arrays has led to the common observation that individuals without a history of pregnancy, transfusion or transplantation can have circulating anti‐HLA antibodies of unknown etiology. We retrospectively analyzed the risk of antibody‐mediated rejection (AMR) and graft outcome in 41 kidney transplant recipients with DSA of unknown etiology (DSA cause‐unk) at the time of transplantation. Twenty‐one patients received a posttransplantation desensitization protocol, and 20 received standard immunosuppressive therapy. The mean number of DSA was 1.4 ± 0.8, ranging from 1 to 5. Complement‐dependent cytotoxicity crossmatches were negative for all the patients. Flow cytometry crossmatches were positive in 47.6% of cases. The incidence of acute AMR was 14.6% at 1 year, regardless of the immunosuppressive regimen. No patients experienced graft loss following AMR. At month 12, across the entire population of patients with DSA cause‐unk, the outcomes were favorable: the measured glomerular filtration rate was 63.8 ± 16.4 mL/min/1.73 m2, the screening biopsies showed low frequencies of microvascular inflammation and no transplant glomerulopathy, and graft and patient survival were 100%. In conclusion, patients with DSA cause‐unk are able to mount AMR but have favorable 1‐year outcomes. This study analyzes kidney transplants performed in recipients with preformed donor‐specific antibodies but without a history of an HLA‐immunizing event, and shows that although these patients may experience antibodymediated rejection, they have a favorable one‐year outcome.
ISSN:	1600-6135 1600-6143