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Clinical implications of anti-HLA antibodies testing in kidney transplantation

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Resumo:Alloantibodies against donor human leukocyte antigens (HLA), termed as donor-specific antibodies (DSA), are one of the most important factors for both early and late kidney allograft dysfunction. In the past, these antibodies were mainly detected through cell-based crossmatch tests. Recently, new techniques such as solid phase immunoassays (SPI) have revealed these antibodies in patient sera with a high degree of detail, previously unimaginable. They have allowed us to accurately determine recipients’ allosensitization status, improve pre-transplant risk assessment with a potential donor and post-transplant alloimmune monitoring. However, the high sensitivity of these new assays has also created areas of uncertainty about their clinical impact. In the pre-transplant setting, the presence of preformed DSA has been associated with an increased risk of antibody-mediated rejection (AMR) and subsequent allograft loss. Nevertheless, several studies have shown that not all DSA are deleterious. Hence, understanding the clinical correlations of DSA characteristics, namely strength, HLA class, complement-fixing ability or IgG subclasses, is paramount for an adequate stratification of the immunological risk at transplant. Furthermore, given that the number of allosensitized patients on waiting lists is increasing, the added information from these new SPI is essential to improve their chance of being transplanted with an admissible immunological risk. After transplantation, the appearance of de novo DSA (dnDSA) has also been associated with a deleterious effect on kidney allograft survival. Moreover, it has been acknowledged that a majority of late allograft failures are caused by alloantibody-driven injury. The current challenges, in this setting, are determining cost-effective DSA screening protocols and understanding which patients could benefit from specific interventions. Furthermore, although therapeutic strategies to control antibody-induced damage remain limited, the longitudinal surveillance of dnDSA emergence and the clinical correlations of their characteristics will play a crucial role in the improvement of late kidney allograft survival.
Autores principais:Malheiro,Jorge
Outros Autores:Tafulo,Sandra
Assunto:allosensitization cell-based crossmatches donor-specific antibodies kidney transplantation solid-phase immunoassays
Ano:2018
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:Fundação para a Ciência e Tecnologia
Idioma:inglês
Origem:SciELO Portugal
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author Malheiro,Jorge
author2 Tafulo,Sandra
author2_role author
author_facet Malheiro,Jorge
Tafulo,Sandra
author_role author
country_str PT
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datacite.creators.creator.creatorName.fl_str_mv Malheiro,Jorge
Tafulo,Sandra
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_abf2
datacite.subjects.subject.fl_str_mv allosensitization
cell-based crossmatches
donor-specific antibodies
kidney transplantation
solid-phase immunoassays
datacite.titles.title.fl_str_mv Clinical implications of anti-HLA antibodies testing in kidney transplantation
dc.creator.none.fl_str_mv Malheiro,Jorge
Tafulo,Sandra
dc.format.none.fl_str_mv text/html
dc.identifier.none.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692018000100007
dc.language.none.fl_str_mv eng
dc.publisher.none.fl_str_mv Sociedade Portuguesa de Nefrologia
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.source.none.fl_str_mv Portuguese Journal of Nephrology & Hypertension v.32 n.1 2018
dc.subject.none.fl_str_mv allosensitization
cell-based crossmatches
donor-specific antibodies
kidney transplantation
solid-phase immunoassays
dc.title.fl_str_mv Clinical implications of anti-HLA antibodies testing in kidney transplantation
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_6501
description Alloantibodies against donor human leukocyte antigens (HLA), termed as donor-specific antibodies (DSA), are one of the most important factors for both early and late kidney allograft dysfunction. In the past, these antibodies were mainly detected through cell-based crossmatch tests. Recently, new techniques such as solid phase immunoassays (SPI) have revealed these antibodies in patient sera with a high degree of detail, previously unimaginable. They have allowed us to accurately determine recipients’ allosensitization status, improve pre-transplant risk assessment with a potential donor and post-transplant alloimmune monitoring. However, the high sensitivity of these new assays has also created areas of uncertainty about their clinical impact. In the pre-transplant setting, the presence of preformed DSA has been associated with an increased risk of antibody-mediated rejection (AMR) and subsequent allograft loss. Nevertheless, several studies have shown that not all DSA are deleterious. Hence, understanding the clinical correlations of DSA characteristics, namely strength, HLA class, complement-fixing ability or IgG subclasses, is paramount for an adequate stratification of the immunological risk at transplant. Furthermore, given that the number of allosensitized patients on waiting lists is increasing, the added information from these new SPI is essential to improve their chance of being transplanted with an admissible immunological risk. After transplantation, the appearance of de novo DSA (dnDSA) has also been associated with a deleterious effect on kidney allograft survival. Moreover, it has been acknowledged that a majority of late allograft failures are caused by alloantibody-driven injury. The current challenges, in this setting, are determining cost-effective DSA screening protocols and understanding which patients could benefit from specific interventions. Furthermore, although therapeutic strategies to control antibody-induced damage remain limited, the longitudinal surveillance of dnDSA emergence and the clinical correlations of their characteristics will play a crucial role in the improvement of late kidney allograft survival.
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person_str_mv Malheiro,Jorge
Tafulo,Sandra
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spelling Clinical implications of anti-HLA antibodies testing in kidney transplantationMalheiro,JorgeTafulo,Sandraallosensitizationcell-based crossmatchesdonor-specific antibodieskidney transplantationsolid-phase immunoassaysopen accesshttp://purl.org/coar/access_right/c_abf2http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692018000100007URLhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692018000100007URLHasVersion2018-03-01Alloantibodies against donor human leukocyte antigens (HLA), termed as donor-specific antibodies (DSA), are one of the most important factors for both early and late kidney allograft dysfunction. In the past, these antibodies were mainly detected through cell-based crossmatch tests. Recently, new techniques such as solid phase immunoassays (SPI) have revealed these antibodies in patient sera with a high degree of detail, previously unimaginable. They have allowed us to accurately determine recipients’ allosensitization status, improve pre-transplant risk assessment with a potential donor and post-transplant alloimmune monitoring. However, the high sensitivity of these new assays has also created areas of uncertainty about their clinical impact. In the pre-transplant setting, the presence of preformed DSA has been associated with an increased risk of antibody-mediated rejection (AMR) and subsequent allograft loss. Nevertheless, several studies have shown that not all DSA are deleterious. Hence, understanding the clinical correlations of DSA characteristics, namely strength, HLA class, complement-fixing ability or IgG subclasses, is paramount for an adequate stratification of the immunological risk at transplant. Furthermore, given that the number of allosensitized patients on waiting lists is increasing, the added information from these new SPI is essential to improve their chance of being transplanted with an admissible immunological risk. After transplantation, the appearance of de novo DSA (dnDSA) has also been associated with a deleterious effect on kidney allograft survival. Moreover, it has been acknowledged that a majority of late allograft failures are caused by alloantibody-driven injury. The current challenges, in this setting, are determining cost-effective DSA screening protocols and understanding which patients could benefit from specific interventions. Furthermore, although therapeutic strategies to control antibody-induced damage remain limited, the longitudinal surveillance of dnDSA emergence and the clinical correlations of their characteristics will play a crucial role in the improvement of late kidney allograft survival.Sociedade Portuguesa de NefrologiaPortuguese Journal of Nephrology & Hypertension v.32 n.1 2018text/htmlengjournal articlehttp://purl.org/coar/resource_type/c_6501literature
spellingShingle Clinical implications of anti-HLA antibodies testing in kidney transplantation
Malheiro,Jorge
allosensitization
cell-based crossmatches
donor-specific antibodies
kidney transplantation
solid-phase immunoassays
status SINGLETON
subject.fl_str_mv allosensitization
cell-based crossmatches
donor-specific antibodies
kidney transplantation
solid-phase immunoassays
title Clinical implications of anti-HLA antibodies testing in kidney transplantation
title_full Clinical implications of anti-HLA antibodies testing in kidney transplantation
title_fullStr Clinical implications of anti-HLA antibodies testing in kidney transplantation
title_full_unstemmed Clinical implications of anti-HLA antibodies testing in kidney transplantation
title_short Clinical implications of anti-HLA antibodies testing in kidney transplantation
title_sort Clinical implications of anti-HLA antibodies testing in kidney transplantation
topic allosensitization
cell-based crossmatches
donor-specific antibodies
kidney transplantation
solid-phase immunoassays
topic_facet allosensitization
cell-based crossmatches
donor-specific antibodies
kidney transplantation
solid-phase immunoassays
url http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692018000100007
visible 1