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Blood levels of donor-specific human leukocyte antigen antibodies after renal transplantation: resolution of rejection in the presence of circulating donor-specific antibody.

Blood levels of donor-specific human leukocyte antigen antibodies after renal transplantation: resolution of rejection in the presence of circulating donor-specific antibody. Research Abstract Details 

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  • Blood levels of donor-specific human leukocyte antigen antibodies after renal transplantation: resolution of rejection in the presence of circulating donor-specific antibody. Abstract Text:

    rob higginsRob Higgins,mark hathawayMark Hathaway,david loweDavid Lowe,for lamFor Lam,habib kashiHabib Kashi,lam chin tanLam Chin Tan,chris imrayChris Imray,simon fletcherSimon Fletcher,daniel zehnderDaniel Zehnder,klaus chenKlaus Chen,nithya krishnanNithya Krishnan,rizwan hamerRizwan Hamer,david briggsDavid Briggs,

    BACKGROUND: Accommodation to antibody is an important mechanism in successful ABO-incompatible transplantation, but its importance in human leukocyte antigen (HLA) antibody-incompatible transplantation is less clear, as sensitive techniques facilitating daily measurement of donor-specific HLA antibodies (DSAs) have only recently been developed. METHODS: We report 24 patients who had HLA antibody-incompatible kidney transplantation (21 living donors, 3 deceased), 21 of whom had pretransplant plasmapheresis. Eight had positive complement-dependent cytotoxic (CDC) crossmatch (XM) pretransplant plasmapheresis, nine had positive flow cytometric (FC) XM, and seven had DSA detectable by microbead analysis only. After transplant, DSA levels were monitored closely with microbead assays. RESULTS: Rejection occurred in five of eight (62.5%) CDC-positive cases, in three of nine (33%) FC-positive cases, and in two of seven (29%) of microbead-only cases at a median of 6.5 days after transplantation. Resolution occurred at a median of 15 days after transplantation, in 8 of 10 cases when the microbead level of DSA had median fluorescence intensity (MFI) >2000 U, in 6 of 10 when the microbead MFI >4000 U. In 8 of 10 cases, the microbead MFI at the time of resolution was greater than at the onset. DSA did not always cause clinical rejection. In five cases with a posttransplant DSA peaking at MFI >2000 U on microbead assay, rejection did not occur. CONCLUSION: These data suggest that the dominant method of successful transplantation was function of the transplant in the presence of circulating DSA, and they also define the period during which this occurred.

    Blood levels of donor-specific human leukocyte antigen antibodies after renal transplantation: resolution of rejection in the presence of circulating donor-specific antibody. Publishing Authors By Initials

    r higginsR Higgins,m hathawayM Hathaway,d loweD Lowe,f lamF Lam,h kashiH Kashi,lc tanLC Tan,c imrayC Imray,s fletcherS Fletcher,d zehnderD Zehnder,k chenK Chen,n krishnanN Krishnan,r hamerR Hamer,d briggsD Briggs,

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    Blood levels of donor-specific human leukocyte antigen antibodies after renal transplantation: resolution of rejection in the presence of circulating donor-specific antibody. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Transplantation

    VOLUME: 84

    Page Numbers: 876-84

    Journal Abbreviation: Transplantation

    ISSN: 0041-1337

    DAY: 15

    MONTH: Oct

    YEAR: 2007

    Blood levels of donor-specific human leukocyte antigen antibodies after renal transplantation: resolution of rejection in the presence of circulating donor-specific antibody. Information

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    LANGUAGE: eng

    NlmUniqueID: 132144

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    Grant and Affiliation Information for Blood levels of donor-specific human leukocyte antigen antibodies after renal transplantation: resolution of rejection in the presence of circulating donor-specific antibody.

    AFFILIATION: Transplant Unit, University Hospitals Coventry and Warwickshire, Coventry, West Midlands, UK. Robert.Higgins@uhcw.nhs.uk

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Transplantation

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