Dissociation of humoral and cellular immune responses in kidney transplant recipients with EBV mucocutaneous ulcer.

EBV positive mucocutaneous ulcer Epstein-Barr virus Post-transplant lymphoproliferative disorder dissociated immune response

Journal

Transplant infectious disease : an official journal of the Transplantation Society
ISSN: 1399-3062
Titre abrégé: Transpl Infect Dis
Pays: Denmark
ID NLM: 100883688

Informations de publication

Date de publication:
Jun 2021
Historique:
revised: 03 12 2020
received: 01 11 2020
accepted: 13 12 2020
pubmed: 23 12 2020
medline: 3 8 2021
entrez: 22 12 2020
Statut: ppublish

Résumé

EBV-positive mucocutaneous ulcer (EBV-MCU) is a rare EBV-positive B-cell lymphoproliferative disorder occurring in immunocompromised patients such as patients with solid organ or hematopoietic stem cells transplantation. EBV-MCU often consists of an isolated and circumscribed cutaneous or mucosal ulcerative lesion with a self-limited growth potential and a high regression rate upon immunosuppressive treatment withdrawal or rituximab therapy. Nevertheless, the pathophysiology of this latent infection leading to clonal lymphoproliferation is not well established. We report here two cases of EBV-MCU in kidney transplant recipients with a dissociated immune response to EBV with the absence of EBV-related antibodies and a positive T-cell response to EBV suggesting a potential specific oncogenic mechanism in this lymphoproliferative disorder.

Identifiants

pubmed: 33352001
doi: 10.1111/tid.13552
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13552

Informations de copyright

© 2020 Wiley Periodicals LLC.

Références

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Auteurs

Pierre Isnard (P)

Department of Nephrology-Transplantation, Necker Enfants Malades Hospital, APHP, Paris, France.
INSERM U1151, Necker Institute, Necker Enfants Malades Hospital, APHP, Paris, France.

Julie Bruneau (J)

Department of Pathology, Necker Enfants Malades Hospital, APHP, Paris, France.
INSERM UMR 1163, Laboratory of Cellular and Molecular Mechanisms of Hematological Disorders and Therapeutic Implications, Paris, France.

Rebecca Sberro-Soussan (R)

Department of Nephrology-Transplantation, Necker Enfants Malades Hospital, APHP, Paris, France.

Dominique Wendum (D)

Department of Pathology, Saint-Antoine Hospital, APHP, Paris, France.

Christophe Legendre (C)

Department of Nephrology-Transplantation, Necker Enfants Malades Hospital, APHP, Paris, France.

Thierry Molina (T)

Department of Pathology, Necker Enfants Malades Hospital, APHP, Paris, France.

Lucienne Chatenoud (L)

Université Paris Descartes, Sorbonne Paris Cité, Paris, France.
INSERM U1151, CNRS UMR 8253, INEM Hôpital Necker-Enfants Malades, Paris, France.
Department of Pathology, Saint Antoine Hospital, APHP, Paris, France.

Olivier Hermine (O)

INSERM UMR 1163, Laboratory of Cellular and Molecular Mechanisms of Hematological Disorders and Therapeutic Implications, Paris, France.
Department of Hematology, Necker Enfants Malades Hospital, APHP, Paris, France.

Julien Rossignol (J)

INSERM UMR 1163, Laboratory of Cellular and Molecular Mechanisms of Hematological Disorders and Therapeutic Implications, Paris, France.
Department of Hematology, Necker Enfants Malades Hospital, APHP, Paris, France.

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