Rituximab therapy for acute humoral rejection after kidney transplantation

A pilot study was performed on eight consecutive renal-transplant (RT) patients presenting with acute humoral rejection (AHR) to assess the efficacy of monoclonal anti-B cell antibodies, such as rituximab (375 mg/m weekly) for 3 to 5 consecutive weeks, in addition to plasma exchange (PE), steroids,...

Full description

Saved in:
Bibliographic Details
Published in:Transplantation Vol. 83; no. 9; pp. 1277 - 1280
Main Authors: FAGUER, Stanislas, KAMAR, Nassim, DURAND, Dominique, ROSTAING, Lionel, GUILBEAUD-FRUGIER, Céline, FORT, Marylise, MODESTO, Anne, MARI, Arnaud, RIBES, David, COINTAULT, Olivier, LAVAYSSIERE, Laurence, GUITARD, Joelle
Format: Journal Article
Language:English
Published: Hagerstown, MD Lippincott 15-05-2007
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:A pilot study was performed on eight consecutive renal-transplant (RT) patients presenting with acute humoral rejection (AHR) to assess the efficacy of monoclonal anti-B cell antibodies, such as rituximab (375 mg/m weekly) for 3 to 5 consecutive weeks, in addition to plasma exchange (PE), steroids, mycophenolate mofetil, and tacrolimus. AHR was associated with increased serum creatinine, the appearance of donor-specific alloantibodies (DSA), and the presence of C4d in a transplant biopsy. After a follow-up of 10 months (range 7-23), patient and graft survivals were 100% and 75%, respectively. Renal function improved in six cases in which serum creatinine decreased from 297+/-140 to 156+/-53 micromol/L (P=0.015); graft loss occurred in two cases; and four patients had infectious complications. At last follow-up, DSA had disappeared or decreased in four cases. Rituximab therapy, in addition to PE, might be of benefit for RT patients presenting with AHR.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ObjectType-Article-2
ObjectType-Feature-1
ISSN:0041-1337
1534-6080
DOI:10.1097/01.tp.0000261113.30757.d1