Evidence map›Paper›PMID 31935197›Full record

ArticleJCI insight2020

Siponimod enriches regulatory T and B lymphocytes in secondary progressive multiple sclerosis.

Qi Wu, Elizabeth A Mills, Qin Wang, Catherine A Dowling, Caitlyn Fisher, Britany Kirch, Steven K Lundy, David A Fox, Yang Mao-Draayer, AMS04 Study Group

Registry-linked trialOpen access · goldAbstract readMulticenter Study
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02330965 (Mechanistic Studies of Phase III Trial With BAF312 in Secondary Progressive Multiple Sclerosis), which is not on this map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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.

NCT02330965 completednot on this map

Mechanistic Studies of Phase III Trial With BAF312 in Secondary Progressive Multiple Sclerosis (AMS04)

TypeobservationalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2014 to 2017Enrolled36ConditionsSecondary Progressive Multiple SclerosisArmsBlood Draw, CSF collection by lumbar puncture (Optional)
3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Siponimod for multiple sclerosis.The Cochrane database of systematic reviews · 2021
    Pooled it
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  17. Current and Future Biomarkers in Multiple Sclerosis.International journal of molecular sciences · 2022
    Review
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  20. Article
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

10 authors at 2 institutions in 2 countries.

Qi WuDepartment of Neurology. AMS04 study group.
Elizabeth A MillsDepartment of Neurology. AMS04 study group.
Qin WangDepartment of Neurology. AMS04 study group.
Catherine A DowlingDepartment of Neurology. AMS04 study group.
Caitlyn FisherDepartment of Neurology. AMS04 study group.
Britany KirchDepartment of Neurology. AMS04 study group.
Steven K LundyAutoimmunity Center of Excellence. AMS04 study group.
David A FoxAutoimmunity Center of Excellence. AMS04 study group.
Yang Mao-DraayerDepartment of Neurology. AMS04 study group.
AMS04 Study Group
Autoimmune Technologies (United States) · USUniversity of Michigan · US

Funding

TRAINING PROGRAM IN ORGANOGENESIST32HD007505 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PASCA DI MAGLIANO, MARINA, SPENCE, JASON · 1997 to 2021
$6.9M
CD24 Targeting for Multiple Sclerosis: a First-In-Human Phase I StudyR01NS080821 · NINDS · ONCOIMMUNE, INC. · PI LIU, YANG · 2013 to 2014
$1.1M
University of Michigan Clinical Autoimmunity Center of ExcellenceUM1AI144298 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FOX, DAVID ALAN, KHANNA, DINESH · 2019 to 2023
$546k
University of Michigan Autoimmunity Center of Excellence, Clinical Research ProgrUM1AI110557 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FOX, DAVID ALAN · 2014 to 2018
$543k
B Cell Exosome and Nanoparticle Treatment of Allergic AsthmaR21AI115117 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUNDY, STEVEN K. · 2015 to 2016
$426k
Enhancing Killer B Lymphocyte Function as a Treatment for Allergic AsthmaR03AI105029 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUNDY, STEVEN K. · 2013 to 2014
$156k
NIAID NIH HHS R03 AI105029NIAID NIH HHS R21 AI115117NIAID NIH HHS UM1 AI110557NIAID NIH HHS UM1 AI144298NICHD NIH HHS T32 HD007505NINDS NIH HHS R01 NS080821
6 · The paper itself

Abstract

BACKGROUNDSiponimod (BAF312) is a selective sphingosine-1-phosphate receptor 1 and 5 (S1PR1, S1PR5) modulator recently approved for active secondary progressive multiple sclerosis (SPMS). The immunomodulatory effects of siponimod in SPMS have not been previously described.METHODSWe conducted a multicentered, randomized, double-blind, placebo-controlled AMS04 mechanistic study with 36 SPMS participants enrolled in the EXPAND trial. Gene expression profiles were analyzed using RNA derived from whole blood with Affymetrix Human Gene ST 2.1 microarray technology. We performed flow cytometry-based assays to analyze the immune cell composition and microarray gene expression analysis on peripheral blood from siponimod-treated participants with SPMS relative to baseline and placebo during the first-year randomization phase.RESULTSMicroarray analysis showed that immune-associated genes involved in T and B cell activation and receptor signaling were largely decreased by siponimod, which is consistent with the reduction in CD4+ T cells, CD8+ T cells, and B cells. Flow cytometric analysis showed that within the remaining lymphocyte subsets there was a reduction in the frequencies of CD4+ and CD8+ naive T cells and central memory cells, while T effector memory cells, antiinflammatory Th2, and T regulatory cells (Tregs) were enriched. Transitional regulatory B cells (CD24hiCD38hi) and B1 cell subsets (CD43+CD27+) were enriched, shifting the balance in favor of regulatory B cells over memory B cells. The proregulatory shift driven by siponimod treatment included a higher proliferative potential of Tregs compared with non-Tregs, and upregulated expression of PD-1 on Tregs. Additionally, a positive correlation was found between Tregs and regulatory B cells in siponimod-treated participants.CONCLUSIONThe shift toward an antiinflammatory and suppressive homeostatic immune system may contribute to the clinical efficacy of siponimod in SPMS.TRIAL REGISTRATIONNCT02330965.

Indexed as

AdolescentAdultAzetidinesBenzyl CompoundsB-LymphocytesDouble-Blind MethodFemaleGene Expression ProfilingHumansMaleMultiple Sclerosis, Chronic ProgressivePlacebosReceptors, LysosphingolipidT-LymphocytesYoung AdultAzetidinesBenzyl CompoundsPlacebosReceptors, LysosphingolipidsiponimodAutoimmunityMultiple sclerosis

Identifiers

PMID31935197
PMCPMC7098784
OpenAlexW2999906211

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.