Circulating B Cells With Memory and Antibody-Secreting Phenotypes Are Detectable in Pediatric Kidney Transplant Recipients Before the Development of Antibody-Mediated Rejection.


Journal

Transplantation direct
ISSN: 2373-8731
Titre abrégé: Transplant Direct
Pays: United States
ID NLM: 101651609

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 10 05 2019
accepted: 16 05 2019
entrez: 4 10 2019
pubmed: 4 10 2019
medline: 4 10 2019
Statut: epublish

Résumé

Development of anti-human leukocyte antigen donor-specific antibodies (DSAs) is associated with antibody-mediated rejection (AMR) and reduced allograft survival in kidney transplant recipients. Whether changes in circulating lymphocytes anticipate DSA or AMR development is unclear. We used time-of-flight mass cytometry to analyze prospectively collected peripheral blood mononuclear cells (PBMC) from pediatric kidney transplant recipients who developed DSA (DSA-positive recipients [DSA DSA Despite the small sample size, our comprehensive phenotypic analyses show that circulating B cells with memory and antibody-secreting phenotypes are present at DSA onset, >1 year before biopsy-proven AMR in pediatric kidney transplant recipients.

Identifiants

pubmed: 31579809
doi: 10.1097/TXD.0000000000000914
pmc: PMC6739044
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e481

Subventions

Organisme : NIDDK NIH HHS
ID : T32 DK007757
Pays : United States

Informations de copyright

Copyright © 2019 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc.

Déclaration de conflit d'intérêts

The authors declare no conflicts of interest.

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Auteurs

Clara Fischman (C)

Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY.

Miguel Fribourg (M)

Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY.

Ginevri Fabrizio (G)

Nephrology, Dialysis and Transplantation Unit, IRCCS Istituto G. Gaslini, Genova, Italy.

Michela Cioni (M)

Nephrology, Dialysis and Transplantation Unit, IRCCS Istituto G. Gaslini, Genova, Italy.

Patrizia Comoli (P)

Pediatric Hematology/Oncology & Cell Factory, Fondazione IRCCS Policlinico S. Matteo, Pavia, Italy.

Arcangelo Nocera (A)

Nephrology, Dialysis and Transplantation Unit, IRCCS Istituto G. Gaslini, Genova, Italy.

Massimo Cardillo (M)

Department Transplantation Immunology, IRCCS Fondazione Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.

Chiara Cantarelli (C)

Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY.
Dipartimento di Medicina e Chirurgia Università di Parma, UO Nefrologia, Azienda Ospedaliera-Universitaria Parma, Parma, Italy.

Lorenzo Gallon (L)

Department of Medicine, Division of Nephrology, Feinberg School of Medicine, Northwestern University, Chicago, IL.

Astgik Petrosyan (A)

Division of Urology GOFARR Laboratory for Organ Regenerative Research and Cell Therapeutics, Children's Hospital Los Angeles, Los Angeles, CA.

Stefano Da Sacco (S)

Division of Urology GOFARR Laboratory for Organ Regenerative Research and Cell Therapeutics, Children's Hospital Los Angeles, Los Angeles, CA.

Laura Perin (L)

Division of Urology GOFARR Laboratory for Organ Regenerative Research and Cell Therapeutics, Children's Hospital Los Angeles, Los Angeles, CA.

Paolo Cravedi (P)

Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY.

Classifications MeSH