Literature DB >> 22592887

Using donor-specific antibodies to monitor the need for immunosuppression.

Junichi Hoshino1, Hugo Kaneku, Matthew J Everly, Sander Greenland, Paul I Terasaki.   

Abstract

BACKGROUND: Experience with tolerance protocols has shown that none is perfect and that each escape from tolerance must be identified early to prevent graft failure. In addition, some test is needed for patients who are weaned off immunosuppression (IS) to forewarn of weaning failure. The usual measures of function--such as serum creatinine levels--are not sensitive enough to detect rejection in a timely manner.
METHODS: A study was carried out on 72 patients who received living-donor kidney transplants with clonal deletion protocol (total lymphoid irradiation or bortezomib), and followed with reduced doses of maintenance IS. Every month or every 2 months, a test was performed for donor-specific antibodies (DSA) using Luminex mixed and/or single antigen beads.
RESULTS: After transplantation, DSA developed in 17% of the patients at 6 months, 41% at 1 year, and 57% at 2 years, with 95% confidence limits of 10%, 28%; 30%, 55%; and 44%, 71%, respectively. Fifty-three percent of patients weaned IS to less than 10 mg prednisone daily experienced DSA within 3 months. Furthermore, prednisone dose (per 2.5 mg) and years after transplantation were inversely associated with DSA production (risk ratio 0.92 [95% confidence limits: 0.85, 0.99], and 0.70 [0.49, 1.00]).
CONCLUSIONS: DSA monitoring is highly effective for detecting escape from tolerance and reemergence of the immune response in weaned patients. DSA appearance was inversely proportional to the level of maintenance drugs in the weaning process. Measurement of DSA on a monthly basis is adequate for detection of the change in immune reactivity.

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Year:  2012        PMID: 22592887     DOI: 10.1097/TP.0b013e31824f3d7c

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  11 in total

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2.  Facilitating cells: Translation of hematopoietic chimerism to achieve clinical tolerance.

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Review 3.  Is it time to give up with calcineurin inhibitors in kidney transplantation?

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Review 4.  ABO-compatible liver allograft antibody-mediated rejection: an update.

Authors:  Anthony J Demetris; Adriana Zeevi; Jacqueline G O'Leary
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5.  Minimization vs tailoring: Where do we stand with personalized immunosuppression during renal transplantation in 2015?

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6.  Alloantibody and autoantibody monitoring predicts islet transplantation outcome in human type 1 diabetes.

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Review 8.  The Influence of Immunosuppressive Agents on the Risk of De Novo Donor-Specific HLA Antibody Production in Solid Organ Transplant Recipients.

Authors:  Jacqueline G OʼLeary; Millie Samaniego; Marta Crespo Barrio; Luciano Potena; Adriana Zeevi; Arjang Djamali; Emanuele Cozzi
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9.  Absolute quantification of donor-derived cell-free DNA as a marker of rejection and graft injury in kidney transplantation: Results from a prospective observational study.

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Journal:  Am J Transplant       Date:  2019-05-28       Impact factor: 8.086

10.  Many de novo donor-specific antibodies recognize β2 -microglobulin-free, but not intact HLA heterodimers.

Authors:  K Michel; R Santella; J Steers; A Sahajpal; F X Downey; V Thohan; M Oaks
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