Evidence map›Paper›PMID 25962509›Full record

ArticleJournal of neuroinflammation2015

Autoantigen cross-reactive environmental antigen can trigger multiple sclerosis-like disease.

Catherine J Reynolds, Malcolm J W Sim, Kathryn J Quigley, Daniel M Altmann, Rosemary J Boyton

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 41% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
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

5 authors at 1 institution in 1 country.

Catherine J ReynoldsLung Immunology Group, Section of Infectious Diseases and Immunity, Division of Infectious Diseases, Department of Medicine, Hammersmith Hospital, Imperial College London, Room 8N22, Commonwealth Building, Du Cane Road, London, W12 ONN, UK. c.reynolds@imperial.ac.uk.
Malcolm J W SimLung Immunology Group, Section of Infectious Diseases and Immunity, Division of Infectious Diseases, Department of Medicine, Hammersmith Hospital, Imperial College London, Room 8N22, Commonwealth Building, Du Cane Road, London, W12 ONN, UK. malcolm.sim06@imperial.ac.uk.
Kathryn J QuigleyLung Immunology Group, Section of Infectious Diseases and Immunity, Division of Infectious Diseases, Department of Medicine, Hammersmith Hospital, Imperial College London, Room 8N22, Commonwealth Building, Du Cane Road, London, W12 ONN, UK. kathryn.quigley09@imperial.ac.uk.
Daniel M AltmannSection of Molecular Immunology, Division of Immunology and Inflammation, Department of Medicine, Hammersmith Hospital, Imperial College London, Du Cane Road, London, W12 ONN, UK. d.altmann@imperial.ac.uk.
Rosemary J BoytonLung Immunology Group, Section of Infectious Diseases and Immunity, Division of Infectious Diseases, Department of Medicine, Hammersmith Hospital, Imperial College London, Room 8N22, Commonwealth Building, Du Cane Road, London, W12 ONN, UK. r.boyton@imperial.ac.uk.
Hammersmith Hospital · GB

Funding

Medical Research CouncilNIAID NIH HHS HHSN272200900046CWellcome TrustWellcome Trust WT095472MA
6 · The paper itself

Abstract

backgroundMultiple sclerosis is generally considered an autoimmune disease resulting from interaction between predisposing genes and environmental factors, together allowing immunological self-tolerance to be compromised. The precise nature of the environmental inputs has been elusive, infectious agents having received considerable attention. A recent study generated an algorithm predicting naturally occurring T cell receptor (TCR) ligands from the proteome database. Taking the example of a multiple sclerosis patient-derived anti-myelin TCR, the study identified a number of stimulatory, cross-reactive peptide sequences from environmental and human antigens. Having previously generated a spontaneous multiple sclerosis (MS) model through expression of this TCR, we asked whether any of these could indeed function in vivo to trigger CNS disease by cross-reactive activation.

findingsA number of myelin epitope cross-reactive epitopes could stimulate T cell immunity in this MS anti-myelin TCR transgenic model. Two of the most stimulatory of these 'environmental' epitopes, from Dictyostyelium slime mold and from Emiliania huxleyi, were tested for the ability to induce MS-like disease in the transgenics. We found that immunization with cross-reactive peptide from Dictyostyelium slime mold (but not from E. huxleyi) induces severe disease.

conclusionsThese specific environmental epitopes are unlikely to be common triggers of MS, but this study suggests that our search for the cross-reactivity triggers of autoimmune activation leading to MS should encompass epitopes not just from the 'infectome' but also from the full environmental 'exposome.'

Indexed as

AnimalsAutoantigensBacterial InfectionsDisease Models, AnimalEnvironmental MicrobiologyHLA-DR Serological SubtypesMiceMice, Inbred C57BLMice, TransgenicMultiple SclerosisMyelin Basic ProteinPertussis ToxinProtozoan InfectionsReceptors, Antigen, T-CellRNA, MessengerT-LymphocytesAutoantigensHLA-DR15 antigenHLA-DR Serological SubtypesMyelin Basic ProteinPertussis ToxinReceptors, Antigen, T-CellRNA, Messenger

Identifiers

PMID25962509
PMCPMC4432996
OpenAlexW2143741739

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.