1976
DOI: 10.1097/00007890-197604000-00006
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Importance of the Autocontrol Crossmatch in Human Renal Transplantation

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Cited by 50 publications
(14 citation statements)
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“…All cell-based assays are subject to falsepositive results caused by autoantibodies and non-HLA antibodies 10,[15][16][17][18][19][20][21] as well as false-negative results when the antibody is very low titer but still has clinical relevance. 22,23 Cell-based assays are now routinely augmented by solid-phase assays, with significantly improved sensitivity and specificity.…”
Section: Cell-based Assays: Detecting Hla Antibodies Before Solid-phamentioning
confidence: 99%
“…All cell-based assays are subject to falsepositive results caused by autoantibodies and non-HLA antibodies 10,[15][16][17][18][19][20][21] as well as false-negative results when the antibody is very low titer but still has clinical relevance. 22,23 Cell-based assays are now routinely augmented by solid-phase assays, with significantly improved sensitivity and specificity.…”
Section: Cell-based Assays: Detecting Hla Antibodies Before Solid-phamentioning
confidence: 99%
“…However, the limitations of the CDC assay have long been appreciated. Because CDC detects antibodies that are not necessarily harmful to a proposed transplant (e.g., immunoglobulin (Ig)-M non-HLAspecific antibodies) [2][3][4][5][6], a positive cross-match may unnecessarily deny transplantation. Conversely, when used in isolation, the CDC test fails to identify renal transplants where there is increased risk of early rather than immediate immunological graft loss.…”
Section: Lymphocytotoxicitymentioning
confidence: 99%
“…If positive results are obtained, a variety of tests can be used to characterize the antibody. A recipient autologous XM should be performed either to rule out autoantibody as the cause of the (+) XM or to determine its impact on the apparent titer of DSA (7, 9). While less common than among recipients, autoantibody may also be present in the donor, potentially yielding a false‐positive result or even making the XM impossible to interpret.…”
Section: Immunologic Risk Assessmentmentioning
confidence: 99%