Evidence map›Paper›PMID 34409288›Full record

ArticleBrain communications2021

Amyotrophic lateral sclerosis transcriptomics reveals immunological effects of low-dose interleukin-2.

Ilaria Giovannelli, Nadhim Bayatti, Abigail Brown, Dennis Wang, Marius Mickunas, William Camu, Jean-Luc Veyrune, Christine Payan, Cecilia Garlanda, Massimo Locati and 16 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Brain communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02059759 (Immuno-modulation in Amyotrophic Lateral Sclerosis- a Phase II Study of Safety and Activity of Low Dose Interleukin-2), which is not on this map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02059759 phase2completednot on this map

Immuno-modulation in Amyotrophic Lateral Sclerosis- a Phase II Study of Safety and Activity of Low Dose Interleukin-2

TypeinterventionalSponsorCentre Hospitalier Universitaire de NīmesRan2015 to 2016Enrolled36ConditionsAmyotrophic Lateral SclerosisArmsPlacebo, 1.0 MIU IL-2 per day, 2.0 MIU IL-2 per day
3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors at 10 institutions in 4 countries.

Ilaria GiovannelliDepartment of Neuroscience, Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield S10 2HQ, UK.ORCID https://orcid.org/0000-0002-5940-5032
Nadhim BayattiDepartment of Neuroscience, Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield S10 2HQ, UK.
Abigail BrownDepartment of Neuroscience, Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield S10 2HQ, UK.
Dennis WangDepartment of Neuroscience, Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield S10 2HQ, UK.
Marius MickunasDepartment of Computer Science, University of Sheffield, Sheffield S1 4DP, UK.
William CamuDepartment of Immunobiology, Faculty of Life Science and Medicine, King's College London, London SE1 9RT, UK.
Jean-Luc VeyruneClinique du Motoneurone, CHU Gui de Chaliac, University of Montpellier, Montpellier 34295, France.
Christine PayanDepartment of Cell and Tissue Engineering, University of Montpellier, CHU Montpellier, Montpellier 34000, France.
Cecilia GarlandaDepartment of Pharmacology, AP-HP Sorbonne University, Pitié-Salpêtrière Hospital, F-75013 Paris, 75013 France.
Massimo LocatiHumanitas University, Pieve Emanuele, Milan 20090, Italy.
Raul Juntas-MoralesDepartment of Immunobiology, Faculty of Life Science and Medicine, King's College London, London SE1 9RT, UK.
Nicolas PageotDepartment of Immunobiology, Faculty of Life Science and Medicine, King's College London, London SE1 9RT, UK.
Andrea MalaspinaDepartment of Neuroimmunology, Barts and the London School of Medicine and Dentistry, Neuroscience and Trauma Centre, Institute of Cell and Molecular Medicine, London E1 2AT, UK.
Ulf AndreassonDepartment of Psychiatry & Neurochemistry, University of Gothenburg, Mölndal 41345, Sweden.
Carey SuehsDepartment of Biostatistics, Clinical Epidemiology, Public Health and Innovation in Methodology (BESPIM), Nîmes University Hospital, Nîmes 30029, France.
Safa SakerDNA and Cell Bank, Genethon, Evry 91000, France.
Christophe MasseguinDelegation for Clinical Research and Innovation, Nîmes University Hospital, Nîmes 30029, France.
John de VosClinique du Motoneurone, CHU Gui de Chaliac, University of Montpellier, Montpellier 34295, France.ORCID https://orcid.org/0000-0003-1880-4130
Henrik ZetterbergDepartment of Psychiatry & Neurochemistry, University of Gothenburg, Mölndal 41345, Sweden.ORCID https://orcid.org/0000-0003-3930-4354
Ammar Al-ChalabiDepartment of Basic and Clinical Neuroscience, Maurice Wohl Clinical Neuroscience Institute, King's College London, London SE5 9RX, UK.ORCID https://orcid.org/0000-0002-4924-7712
P Nigel LeighBrighton and Sussex Medical School, The Trafford Centre for Biomedical Research, Falmer, Brighton BN1 9RY, UK.
Timothy TreeDepartment of Computer Science, University of Sheffield, Sheffield S1 4DP, UK.
Gilbert BensimonDepartment of Cell and Tissue Engineering, University of Montpellier, CHU Montpellier, Montpellier 34000, France.
Paul R HeathDepartment of Neuroscience, Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield S10 2HQ, UK.
Pamela J ShawDepartment of Neuroscience, Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield S10 2HQ, UK.
Janine KirbyDepartment of Neuroscience, Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield S10 2HQ, UK.ORCID https://orcid.org/0000-0002-7468-5917
University of Sheffield · GBKing's College London · GBUniversité de Montpellier · FRHumanitas University · ITBrighton and Sussex Medical School · GBGenethon (France) · FRQueen Mary University of London · GBSahlgrenska University Hospital · SEUniversité de Nîmes · FRUniversity of Gothenburg · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amyotrophic lateral sclerosis is a fatal neurodegenerative disease causing upper and lower motor neuron loss and currently no effective disease-modifying treatment is available. A pathological feature of this disease is neuroinflammation, a mechanism which involves both CNS-resident and peripheral immune system cells. Regulatory T-cells are immune-suppressive agents known to be dramatically and progressively decreased in patients with amyotrophic lateral sclerosis. Low-dose interleukin-2 promotes regulatory T-cell expansion and was proposed as an immune-modulatory strategy for this disease. A randomized placebo-controlled pilot phase-II clinical trial called Immuno-Modulation in Amyotrophic Lateral Sclerosis was carried out to test safety and activity of low-dose interleukin-2 in 36 amyotrophic lateral sclerosis patients (NCT02059759). Participants were randomized to 1MIU, 2MIU-low-dose interleukin-2 or placebo and underwent one injection daily for 5 days every 28 days for three cycles. In this report, we describe the results of microarray gene expression profiling of trial participants' leukocyte population. We identified a dose-dependent increase in regulatory T-cell markers at the end of the treatment period. Longitudinal analysis revealed an alteration and inhibition of inflammatory pathways occurring promptly at the end of the first treatment cycle. These responses are less pronounced following the end of the third treatment cycle, although an activation of immune-regulatory pathways, involving regulatory T-cells and T helper 2 cells, was evident only after the last cycle. This indicates a cumulative effect of repeated low-dose interleukin-2 administration on regulatory T-cells. Our analysis suggested the existence of inter-individual variation amongst trial participants and we therefore classified patients into low, moderate and high-regulatory T-cell-responders. NanoString profiling revealed substantial baseline differences between participant immunological transcript expression profiles with the least responsive patients showing a more inflammatory-prone phenotype at the beginning of the trial. Finally, we identified two genes in which pre-treatment expression levels correlated with the magnitude of drug responsiveness. Therefore, we proposed a two-biomarker based regression model able to predict patient regulatory T-cell-response to low-dose interleukin-2. These findings and the application of this methodology could be particularly relevant for future precision medicine approaches to treat amyotrophic lateral sclerosis.

Indexed as

amyotrophic lateral sclerosisclinical triallow-dose interleukin 2regulatory T cellstranscriptomics

Identifiers

PMID34409288
PMCPMC8364666
OpenAlexW3174367383

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.