Progressive multifocal leukoencephalopathy after durvalumab treatment for acute myeloid leukemia: A consequence of an immune reconstitution inflammatory syndrome?

acute leukemia immunopathology immunotherapy infection

Journal

EJHaem
ISSN: 2688-6146
Titre abrégé: EJHaem
Pays: United States
ID NLM: 101761942

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 02 05 2022
revised: 11 05 2022
accepted: 12 05 2022
entrez: 2 9 2022
pubmed: 3 9 2022
medline: 3 9 2022
Statut: epublish

Résumé

Progressive multifocal leukoencephalopathy (PML) is a fatal demyelinating disease of the central nervous system resulting from the reactivation of the John Cunningham virus (JCV). PML occurs almost exclusively during profound immune suppression but it can also be observed in immunocompromised subjects as part of an inflammatory immune reconstitution syndrome (IRIS) in patients receiving antiviral therapy. We report a case of PML in a 61-year-old patient with acute myeloid leukemia who had developed after discontinuation of durvalumab (anti-PD-L1) therapy initiated after multiple treatments. Results suggest that PML may result from two nonexclusive mechanisms: (i) an inhibition of the protective response of JCV-specific T cells as a consequence of the blockade of the PD1-PDL1 pathway, associated with a lack of compensatory expression of other inhibitory receptors by T cells and (ii) a neuroinflammatory response (PML-IRIS) that may have contributed to virus reactivation.

Identifiants

pubmed: 36051020
doi: 10.1002/jha2.485
pii: JHA2485
pmc: PMC9422031
doi:

Types de publication

Journal Article

Langues

eng

Pagination

958-961

Informations de copyright

© 2022 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Emeline Vinatier (E)

CHU Angers Laboratoire d'Immunologie et Allergologie Angers France.
Univ Angers Nantes Université CHU Angers INSERM CNRS CRCI2NA SFR ICAT Angers France.

Caroline Poli (C)

CHU Angers Laboratoire d'Immunologie et Allergologie Angers France.
Univ Angers Nantes Université CHU Angers INSERM CNRS CRCI2NA SFR ICAT Angers France.

Aurélien Giltat (A)

CHU Angers Service des maladies du sang Angers France.

Christopher Nunes-Gomes (C)

CHU Angers Service des maladies du sang Angers France.

Corentin Orvain (C)

Univ Angers Nantes Université CHU Angers INSERM CNRS CRCI2NA SFR ICAT Angers France.
CHU Angers Service des maladies du sang Angers France.

Mathilde Hunault-Berger (M)

Univ Angers Nantes Université CHU Angers INSERM CNRS CRCI2NA SFR ICAT Angers France.
CHU Angers Service des maladies du sang Angers France.

Pascale Jeannin (P)

CHU Angers Laboratoire d'Immunologie et Allergologie Angers France.
Univ Angers Nantes Université CHU Angers INSERM CNRS CRCI2NA SFR ICAT Angers France.

Sylvain Thépot (S)

Univ Angers Nantes Université CHU Angers INSERM CNRS CRCI2NA SFR ICAT Angers France.
CHU Angers Service des maladies du sang Angers France.

Classifications MeSH