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Impact of donor extracellular vesicle release on recipient cell "cross-dressing" following clinical liver and kidney transplantation.
Mastoridis, Sotiris; Londoño, María-Carlota; Kurt, Ada; Kodela, Elisavet; Crespo, Elena; Mason, John; Bestard, Oriol; Martínez-Llordella, Marc; Sánchez-Fueyo, Alberto.
Afiliación
  • Mastoridis S; Medical Research Council (MRC) Centre for Transplantation, Institute of Liver Studies, King's College London, London, United Kingdom.
  • Londoño MC; Medical Research Council (MRC) Centre for Transplantation, Institute of Liver Studies, King's College London, London, United Kingdom.
  • Kurt A; Liver Unit, Hospital Clinic Barcelona, IDIBAPS, CIBEREHD, Barcelona, Spain.
  • Kodela E; Medical Research Council (MRC) Centre for Transplantation, Institute of Liver Studies, King's College London, London, United Kingdom.
  • Crespo E; Medical Research Council (MRC) Centre for Transplantation, Institute of Liver Studies, King's College London, London, United Kingdom.
  • Mason J; Kidney Transplant Unit, Bellvitge University Hospital, Barcelona, Spain.
  • Bestard O; Department of Physiology, Anatomy & Genetics, University of Oxford, United Kingdom.
  • Martínez-Llordella M; Kidney Transplant Unit, Bellvitge University Hospital, Barcelona, Spain.
  • Sánchez-Fueyo A; Medical Research Council (MRC) Centre for Transplantation, Institute of Liver Studies, King's College London, London, United Kingdom.
Am J Transplant ; 21(7): 2387-2398, 2021 07.
Article en En | MEDLINE | ID: mdl-32515541
In several murine models of transplantation, the "cross-dressing" of recipient antigen presenting cells (APCs) with intact donor major histocompatibility complex (MHC) derived from allograft-released small extracellular vesicles (sEVs) has been recently described as a key mechanism in eliciting and sustaining alloimmune responses. Investigation of these processes in clinical organ transplantation has, however, been hampered by the lack of sensitivity of conventional instruments and assays. We have employed advanced imaging flow cytometry (iFCM) to explore the kinetics of allograft sEV release and the extent to which donor sEVs might induce cross-dressing following liver and kidney transplantation. We report for the first time that recipient APC cross-dressing can be transiently detected in the circulation shortly after liver, but not kidney, transplantation in association with the release of HLA-bearing allograft-derived sEVs. In liver transplant recipients the majority of circulating cells exhibiting donor HLA are indeed cross-dressed cells and not passenger leukocytes. In keeping with experimental animal data, the downstream functional consequences of the transfer of circulating sEVs harvested from human transplant recipients varies depending on the type of transplant and time posttransplant. sEVs released shortly after liver, but not kidney, transplantation exhibit immunoinhibitory effects that could influence liver allograft immunogenicity.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trasplante de Riñón / Vesículas Extracelulares Tipo de estudio: Etiology_studies Límite: Animals / Humans Idioma: En Revista: Am J Transplant Asunto de la revista: TRANSPLANTE Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trasplante de Riñón / Vesículas Extracelulares Tipo de estudio: Etiology_studies Límite: Animals / Humans Idioma: En Revista: Am J Transplant Asunto de la revista: TRANSPLANTE Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos