179.[20230215]Desensitization in Crossmatch-positive KT
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작성자 신호식 작성일23-02-03 14:25 조회528회 댓글0건관련링크
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Review Transplantation
. 2023 Feb 1;107(2):351-360. doi: 10.1097/TP.0000000000004279. Epub 2022 Aug 5.
Desensitization in Crossmatch-positive Kidney Transplant Candidates
Johan Noble 1 2, Thomas Jouve 1 2, Paolo Malvezzi 1, Lionel Rostaing 1 2 3
Affiliations expand
PMID: 35939390 DOI: 10.1097/TP.0000000000004279
Abstract
Access to kidney transplantation is limited by HLA-specific sensitization. Desensitization strategies enable crossmatch-positive kidney transplantation. In this review, we describe clinical experience gained over the last 20 y using desensitization strategies before kidney transplantation and describe the different tools used (both drugs and apheresis options), including IVIg, rituximab, apheresis techniques, interleukin-6 interference, proteasome inhibition, enzymatic degradation of HLA antibodies, complement inhibition, and B cytokine interference. Although access to transplantation for highly sensitized kidney transplantation candidates has been vastly improved by desensitization strategies, it remains, however, limited by the recurrence of HLA antibodies after transplantation and the occurrence of antibody-mediated rejection.
Review Transplantation
. 2023 Feb 1;107(2):351-360. doi: 10.1097/TP.0000000000004279. Epub 2022 Aug 5.
Desensitization in Crossmatch-positive Kidney Transplant Candidates
Johan Noble 1 2, Thomas Jouve 1 2, Paolo Malvezzi 1, Lionel Rostaing 1 2 3
Affiliations expand
PMID: 35939390 DOI: 10.1097/TP.0000000000004279
Abstract
Access to kidney transplantation is limited by HLA-specific sensitization. Desensitization strategies enable crossmatch-positive kidney transplantation. In this review, we describe clinical experience gained over the last 20 y using desensitization strategies before kidney transplantation and describe the different tools used (both drugs and apheresis options), including IVIg, rituximab, apheresis techniques, interleukin-6 interference, proteasome inhibition, enzymatic degradation of HLA antibodies, complement inhibition, and B cytokine interference. Although access to transplantation for highly sensitized kidney transplantation candidates has been vastly improved by desensitization strategies, it remains, however, limited by the recurrence of HLA antibodies after transplantation and the occurrence of antibody-mediated rejection.
