101.[20221129]Memory B cells and long-lived plasma cells in AMR
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작성자 신호식 작성일23-02-03 13:54 조회474회 댓글0건관련링크
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Review Ren Fail
. 2022 Dec;44(1):1604-1614. doi: 10.1080/0886022X.2022.2128374.
Memory B cells and long-lived plasma cells in AMR
Wenlong Yue 1, Jia Liu 2, Xiaohu Li 1, Luman Wang 3, Jinfeng Li 1
Affiliations expand
PMID: 36190837 PMCID: PMC9542532 DOI: 10.1080/0886022X.2022.2128374
Free PMC article
Abstract
Antibody-mediated rejection (AMR) has a strongly negative impact on long-term renal allograft survival. Currently, no recognized effective treatments are available, especially for chronic antibody-mediated rejection (CAMR). Donor-specific antibodies (DSAs) secreted by long-lived plasma cells and memory B cells are acknowledged as biomarkers of AMR. Nevertheless, it may be too late for the DSA routine examination production since DSAs may have binded to graft vascular endothelial cells through complement-dependent or complement-independent pathways. Therefore, methods to effectively monitor memory B cells and long-lived plasma cells and subsequently prevent DSA production are key to reducing the adverse effects of AMR. Therefore, this review mainly summarizes the production pathways of memory B cells and long-lived plasma cells and provides suggestions for the prevention of AMR after transplantation.
Keywords: Antibody-mediated rejection; long-lived plasma cells; memory B cells.
Review Ren Fail
. 2022 Dec;44(1):1604-1614. doi: 10.1080/0886022X.2022.2128374.
Memory B cells and long-lived plasma cells in AMR
Wenlong Yue 1, Jia Liu 2, Xiaohu Li 1, Luman Wang 3, Jinfeng Li 1
Affiliations expand
PMID: 36190837 PMCID: PMC9542532 DOI: 10.1080/0886022X.2022.2128374
Free PMC article
Abstract
Antibody-mediated rejection (AMR) has a strongly negative impact on long-term renal allograft survival. Currently, no recognized effective treatments are available, especially for chronic antibody-mediated rejection (CAMR). Donor-specific antibodies (DSAs) secreted by long-lived plasma cells and memory B cells are acknowledged as biomarkers of AMR. Nevertheless, it may be too late for the DSA routine examination production since DSAs may have binded to graft vascular endothelial cells through complement-dependent or complement-independent pathways. Therefore, methods to effectively monitor memory B cells and long-lived plasma cells and subsequently prevent DSA production are key to reducing the adverse effects of AMR. Therefore, this review mainly summarizes the production pathways of memory B cells and long-lived plasma cells and provides suggestions for the prevention of AMR after transplantation.
Keywords: Antibody-mediated rejection; long-lived plasma cells; memory B cells.