First use of imlifidase desensitization in a highly sensitized lung transplant candidate: a case report.

clinical research/practice crossmatch desensitization histocompatibility immunosuppressant–other immunosuppression/immune modulation lung transplantation/pulmonology panel reactive antibody (PRA) rejection: antibody-mediated (ABMR)

Journal

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
ISSN: 1600-6143
Titre abrégé: Am J Transplant
Pays: United States
ID NLM: 100968638

Informations de publication

Date de publication:
02 2023
Historique:
received: 27 06 2022
revised: 10 10 2022
accepted: 13 11 2022
pubmed: 26 1 2023
medline: 25 2 2023
entrez: 25 1 2023
Statut: ppublish

Résumé

Lung transplant candidates who are highly sensitized against human leucocyte antigen present an ongoing challenge with regards to finding immunologically acceptable donors. Desensitization strategies aimed at reducing preformed donor-specific antibodies have a number of limitations. Imlifidase, an IgG-degrading enzyme derived from Streptococcus pyogenes, is a novel agent that has been used to convert positive crossmatches to negative in kidney transplant candidates, allowing transplantation to occur. We present the first case of imlifidase use for antibody depletion in a highly sensitized lung transplant candidate who went on to undergo a successful bilateral lung transplant.

Identifiants

pubmed: 36695676
pii: S1600-6135(22)29297-1
doi: 10.1016/j.ajt.2022.11.025
pii:
doi:

Substances chimiques

Antibodies 0
Immunosuppressive Agents 0
HLA Antigens 0

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

294-297

Informations de copyright

Copyright © 2022 American Society of Transplantation & American Society of Transplant Surgeons. Published by Elsevier Inc. All rights reserved.

Auteurs

Antoine Roux (A)

Pneumology, Adult Cystic Fibrosis Center and Lung Transplantation Department, Foch Hospital, Suresnes, France; UMR 0892, Université Versailles-Saint-Quentin-en-Yvelines, Versailles, France; Paris Transplant Group, INSERM U 970s, Paris, France. Electronic address: rouxantoine@hotmail.com.

Vincent Bunel (V)

Pneumology Department, Bichat Hospital, Paris, France.

Natalia Belousova (N)

Pneumology, Adult Cystic Fibrosis Center and Lung Transplantation Department, Foch Hospital, Suresnes, France.

Jonathan Messika (J)

Pneumology Department, Bichat Hospital, Paris, France.

Sebastien Tanaka (S)

Intensive Care Department, Bichat Hospital, Paris, France.

Mathilde Salpin (M)

Pneumology Department, Bichat Hospital, Paris, France.

Arnaud Roussel (A)

Thoracic Surgery Department, Bichat Hospital, Paris, France.

Laurence Beaumont-Azuar (L)

Pneumology, Adult Cystic Fibrosis Center and Lung Transplantation Department, Foch Hospital, Suresnes, France.

Clement Picard (C)

Pneumology, Adult Cystic Fibrosis Center and Lung Transplantation Department, Foch Hospital, Suresnes, France.

Olivier Brugiere (O)

Pneumology, Adult Cystic Fibrosis Center and Lung Transplantation Department, Foch Hospital, Suresnes, France.

Jerome Devaquet (J)

Intensive Care Unit, Foch Hospital, Suresnes, France.

Edouard Sage (E)

Thoracic Surgery Department, Foch Hospital, Suresnes, France.

Morgan Le Guen (M)

Anesthesiology Department, Foch Hospital, Suresnes, France.

Jean-Luc Taupin (JL)

Laboratoire Régional d'Histocompatibilité, Saint-Louis Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.

Magali Devriese (M)

Laboratoire Régional d'Histocompatibilité, Saint-Louis Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.

Mathieu Glorion (M)

Thoracic Surgery Department, Foch Hospital, Suresnes, France.

Francois Parquin (F)

Thoracic Intensive Care Unit, Foch Hospital, Suresnes, France.

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Classifications MeSH