2017
DOI: 10.1016/j.transproceed.2017.04.016
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Flow Cytometry Panel-Reactive Antibody Screening of Anti-HLA Antibodies in the Waiting List Significantly Reduces the Occurrence of Acute Rejection After Kidney Transplantation

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“…Depending on the recommendations in individual countries, various methods are used, starting from the biological method PRA-CDC (Panel Reactive Antibodies-Complement Dependent Cytotoxicity) performed in the potential recipient from the moment of entering the transplant waiting list until the procedure is performed, through tests with higher resolution, such as SPA (Solid Phase Assay) using a flow fluorimeter (Luminex), flow cytometer or ELISA technique, allowing to identify the specificity of anti-HLA antibodies and differentiate their classes [2,8,16,17]. These tests should include assessing antibodies in the group of potential recipients and monitoring the humoral response in transplant patients.…”
Section: Discussionmentioning
confidence: 99%
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“…Depending on the recommendations in individual countries, various methods are used, starting from the biological method PRA-CDC (Panel Reactive Antibodies-Complement Dependent Cytotoxicity) performed in the potential recipient from the moment of entering the transplant waiting list until the procedure is performed, through tests with higher resolution, such as SPA (Solid Phase Assay) using a flow fluorimeter (Luminex), flow cytometer or ELISA technique, allowing to identify the specificity of anti-HLA antibodies and differentiate their classes [2,8,16,17]. These tests should include assessing antibodies in the group of potential recipients and monitoring the humoral response in transplant patients.…”
Section: Discussionmentioning
confidence: 99%
“…These tests should include assessing antibodies in the group of potential recipients and monitoring the humoral response in transplant patients. Determination of anti-HLA specificity before transplantation allows for calculating the virtual PRA, enabling precise donor selection, even for highly immunised recipients [17,18]. In addition, the use of this test after transplantation may facilitate monitoring of the level of alloimmunisation, as well as allowing the detection and assessment of the level of DSA-specific antibodies synthesised de novo in the patient.…”
Section: Discussionmentioning
confidence: 99%
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