Immunological and clinical effects of low-dose interleukin-2 across 11 autoimmune diseases in a single, open clinical trial.


Journal

Annals of the rheumatic diseases
ISSN: 1468-2060
Titre abrégé: Ann Rheum Dis
Pays: England
ID NLM: 0372355

Informations de publication

Date de publication:
02 2019
Historique:
received: 02 08 2018
revised: 29 10 2018
accepted: 01 11 2018
pubmed: 26 11 2018
medline: 29 10 2019
entrez: 26 11 2018
Statut: ppublish

Résumé

Regulatory T cells (Tregs) prevent autoimmunity and control inflammation. Consequently, any autoimmune or inflammatory disease reveals a Treg insufficiency. As low-dose interleukin-2 (ld-IL2) expands and activates Tregs, it has a broad therapeutic potential. We aimed to assess this potential and select diseases for further clinical development by cross-investigating the effects of ld-IL2 in a single clinical trial treating patients with 1 of 11 autoimmune diseases. We performed a prospective, open-label, phase I-IIa study in 46 patients with a mild to moderate form of either rheumatoid arthritis, ankylosing spondylitis, systemic lupus erythematosus, psoriasis, Behcet's disease, granulomatosis with polyangiitis, Takayasu's disease, Crohn's disease, ulcerative colitis, autoimmune hepatitis and sclerosing cholangitis. They all received ld-IL2 (1 million IU/day) for 5 days, followed by fortnightly injections for 6 months. Patients were evaluated by deep immunomonitoring and clinical evaluation. ld-IL2 was well tolerated whatever the disease and the concomitant treatments. Thorough supervised and unsupervised immunomonitoring demonstrated specific Treg expansion and activation in all patients, without effector T cell activation. Indication of potential clinical efficacy was observed. The dose of IL-2 and treatment scheme used selectively activate and expand Tregs and are safe across different diseases and concomitant treatments. This and preliminary indications of clinical efficacy should licence the launch of phase II efficacy trial of ld-IL2 in various autoimmune and inflammatory diseases. NCT01988506.

Identifiants

pubmed: 30472651
pii: annrheumdis-2018-214229
doi: 10.1136/annrheumdis-2018-214229
doi:

Substances chimiques

Immunologic Factors 0
Interleukin-2 0

Banques de données

ClinicalTrials.gov
['NCT01988506']

Types de publication

Clinical Trial, Phase I Clinical Trial, Phase II Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

209-217

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: MR, RL, PC, FB, BF, PC, JS, DS, CB and DK are inventors for patent applications related to the therapeutic use of ld-IL2, which belongs to their academic institutions and has been licensed to ILTOO Pharma. MR, VD, JM and DK hold shares in ILTOO Pharma. HPP, VD and JM are employees of ILTOO Pharma. No other potential conflicts of interest relevant to this article were reported.

Auteurs

Michelle Rosenzwajg (M)

Inflammation-Immunopathology-Biotherapy Department (i2B), AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
Immunology-Immunopathology- Immunotherapy (i3), Sorbonne Université, INSERM, Paris, France.

Roberta Lorenzon (R)

Inflammation-Immunopathology-Biotherapy Department (i2B), AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
Immunology-Immunopathology- Immunotherapy (i3), Sorbonne Université, INSERM, Paris, France.

Patrice Cacoub (P)

Inflammation-Immunopathology-Biotherapy Department (i2B), AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
Immunology-Immunopathology- Immunotherapy (i3), Sorbonne Université, INSERM, Paris, France.
Department of Internal Medicine and Clinical Immunology, AP-HP, Pitié-Salpêtrière Hospital, Paris, France.

Hang Phuong Pham (HP)

ILTOO Pharma, Paris, France.

Fabien Pitoiset (F)

Inflammation-Immunopathology-Biotherapy Department (i2B), AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
Immunology-Immunopathology- Immunotherapy (i3), Sorbonne Université, INSERM, Paris, France.

Karim El Soufi (K)

Inflammation-Immunopathology-Biotherapy Department (i2B), AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
Immunology-Immunopathology- Immunotherapy (i3), Sorbonne Université, INSERM, Paris, France.

Claire RIbet (C)

Inflammation-Immunopathology-Biotherapy Department (i2B), AP-HP, Pitié-Salpêtrière Hospital, Paris, France.

Claude Bernard (C)

Inflammation-Immunopathology-Biotherapy Department (i2B), AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
Immunology-Immunopathology- Immunotherapy (i3), Sorbonne Université, INSERM, Paris, France.

Selim Aractingi (S)

Department of Dermatology, AP-HP Cochin Hospital, Paris, France.

Beatrice Banneville (B)

Department of Rheumatology, AP-HP Pitié-Salpêtrière Hospital, Paris, France.

Laurent Beaugerie (L)

Department of Gastroenterology, AP-HP Saint Antoine Hospital, Paris, France.

Francis Berenbaum (F)

Department of Rheumatology, AP-HP Saint-Antoine Hospital, Paris, France.

Julien Champey (J)

Department of Rheumatology, AP-HP Saint-Antoine Hospital, Paris, France.

Olivier Chazouilleres (O)

Department of Hepatology, AP-HP Saint-Antoine Hospital, Paris, France.

Christophe Corpechot (C)

Department of Hepatology, AP-HP Saint-Antoine Hospital, Paris, France.

Bruno Fautrel (B)

Department of Rheumatology, AP-HP Pitié-Salpêtrière Hospital, Paris, France.

Arsène Mekinian (A)

Department of Internal Medicine, AP-HP, Saint-Antoine Hospital, Paris, France.

Elodie Regnier (E)

Department of Dermatology, AP-HP Cochin Hospital, Paris, France.

David Saadoun (D)

Inflammation-Immunopathology-Biotherapy Department (i2B), AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
Immunology-Immunopathology- Immunotherapy (i3), Sorbonne Université, INSERM, Paris, France.
Department of Internal Medicine and Clinical Immunology, AP-HP, Pitié-Salpêtrière Hospital, Paris, France.

Joe-Elie Salem (JE)

Department of Pharmacology and CIC-1421, AP-HP Pitié-Salpêtrière Hospital, Paris, France.

Jérémie Sellam (J)

Department of Rheumatology, AP-HP Saint-Antoine Hospital, Paris, France.

Philippe Seksik (P)

Department of Gastroenterology, AP-HP Saint Antoine Hospital, Paris, France.

Anne Daguenel-Nguyen (A)

Department of Pharmacy, AP-HP Saint-Antoine Hospital, Paris, France.

Valérie Doppler (V)

ILTOO Pharma, Paris, France.

Jéremie Mariau (J)

ILTOO Pharma, Paris, France.

Eric Vicaut (E)

Unité de Recherche Clinique and Université Paris, AP-HP Saint Louis/Lariboisière Hospitals, Paris, France.

David Klatzmann (D)

Inflammation-Immunopathology-Biotherapy Department (i2B), AP-HP, Pitié-Salpêtrière Hospital, Paris, France david.klatzmann@sorbonne-universite.fr.
Immunology-Immunopathology- Immunotherapy (i3), Sorbonne Université, INSERM, Paris, France.

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