Low dose IL-2 in patients with steroid-dependent dysimmune manifestations associated with myelodysplastic syndromes: a three-case report.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
01 07 2021
Historique:
received: 29 05 2020
revised: 19 09 2020
pubmed: 10 11 2020
medline: 24 8 2021
entrez: 9 11 2020
Statut: ppublish

Résumé

Systemic inflammatory and autoimmune diseases can be associated with myelodysplastic syndromes. Current treatments (steroids, immunosuppressive agents, biologics) are unsatisfactory because of their low response rate, dependence or adverse events. We aimed at evaluating the effects of low doses of IL-2 (ld-IL2) as a regulatory T-cell inducer in this context. We treated three patients with ld-IL2 with myelodysplastic syndromes and an associated dysimmune disorder (polymyalgia rheumatic, relapsing polychondritis associated with Sweet's syndrome and vasculitis with cutaneous and joint involvement, respectively). All three patients were dependent on steroids and refractory to biologics or azacitidine. They received doses of 1-1.5 million units of proleukin/day during 5 days and then every fortnight. The treatment led to a clinical improvement and steroid sparing in 2/3 patients with no serious adverse events, and no progression of the disease. Our results support the investigation of ld-IL2 in MDS associated with immune disorders in controlled clinical studies.

Identifiants

pubmed: 33164099
pii: 5961489
doi: 10.1093/rheumatology/keaa696
doi:

Substances chimiques

Glucocorticoids 0
Interleukin-2 0

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3404-3408

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Marion Corfmat (M)

Service de Médecine Interne, IUCT Oncopôle, Centre Hospitalier Universitaire de Toulouse, Toulouse.

Christophe Willekens (C)

Département d'Hématologie, Institut Gustave Roussy, Université Paris Sud, Villejuif.

Julien Vinit (J)

Service de Médecine Interne, CHWM, 4, Rue Capitaine-Drillien, Chalon-sur-Saône.

Guillaume Bussone (G)

Service de Médecine Interne, Immunologie Clinique, Médecine Aigüe Polyvalente, Hôpital Antoine-Béclère-AP-HP, Clamart.

Pierre Fenaux (P)

Service d'Hématologie Séniors Hôpital Saint-Louis, Assistance Publique - Hôpitaux de Paris, Université de Paris.

Olivier Fain (O)

Service de Médecine Interne, AP-HP, Hôpital Saint Antoine, Sorbonne Université.

David Klatzmann (D)

INSERM, Immunology-Immunopathology-Immunotherapy (i3), Sorbonne Université.
Clinical Investigation Center for Biotherapies (CIC-BTi) and Immunology-Inflammation-Infectiology and Dermatology Department (3iD), AP-HP, Hôpital Pitié-Salpêtrière, Paris.

Arsene Mekinian (A)

Service de Médecine Interne, AP-HP, Hôpital Saint Antoine, Sorbonne Université.

Thibault Comont (T)

Service de Médecine Interne, IUCT Oncopôle, Centre Hospitalier Universitaire de Toulouse, Toulouse.
Centre de Recherche en Cancérologie de Toulouse, Inserm UMR 1037, Toulouse, France.

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Classifications MeSH