Evidence map›Paper›PMID 19050840›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2009

Brain antigens in functionally distinct antigen-presenting cell populations in cervical lymph nodes in MS and EAE.

Marloes van Zwam, Ruth Huizinga, Marie-José Melief, Annet F Wierenga-Wolf, Marjan van Meurs, Jane S Voerman, Knut P H Biber, Hendrikus W G M Boddeke, Uta E Höpken, Christian Meisel and 7 more

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In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

81 citing papers in PubMed, 138 citations in OpenAlex.

  1. Trial
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  3. The cribriform plate: A dynamic central nervous system-immune hub.The Journal of experimental medicine · 2026
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  6. SPIONActa neuropathologica communications · 2025
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21 more citing papers are in PubMed but not listed here.

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

17 authors at 8 institutions in 2 countries.

Marloes van ZwamDepartment of Immunology, Erasmus MC, CA, Rotterdam, The Netherlands.
Ruth Huizinga
Marie-José Melief
Annet F Wierenga-Wolf
Marjan van Meurs
Jane S Voerman
Knut P H Biber
Hendrikus W G M Boddeke
Uta E Höpken
Christian Meisel
Andreas Meisel
Ingo Bechmann
Rogier Q Hintzen
Bert A 't Hart
Sandra Amor
Jon D Laman
Leonie A Boven
Erasmus University Rotterdam · NLCharité - Universitätsmedizin Berlin · DEErasmus MC · NLUniversity Medical Center Groningen · NLAmsterdam UMC Location VUmc · NLBiomedical Primate Research Centre · NLGoethe University Frankfurt · DEMax Delbrück Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drainage of central nervous system (CNS) antigens to the brain-draining cervical lymph nodes (CLN) is likely crucial in the initiation and control of autoimmune responses during multiple sclerosis (MS). We demonstrate neuronal antigens within CLN of MS patients. In monkeys and mice with experimental autoimmune encephalomyelitis (EAE) and in mouse models with non-inflammatory CNS damage, the type and extent of CNS damage was associated with the frequencies of CNS antigens within the cervical lymph nodes. In addition, CNS antigens drained to the spinal-cord-draining lumbar lymph nodes. In human MS CLN, neuronal antigens were present in pro-inflammatory antigen-presenting cells (APC), whereas the majority of myelin-containing cells were anti-inflammatory. This may reflect a different origin of the cells or different drainage mechanisms. Indeed, neuronal antigen-containing cells in human CLN did not express the lymph node homing receptor CCR7, whereas myelin antigen-containing cells in situ and in vitro did. Nevertheless, CLN from EAE-affected CCR7-deficient mice contained equal amounts of myelin and neuronal antigens as wild-type mice. We conclude that the type and frequencies of CNS antigens within the CLN are determined by the type and extent of CNS damage. Furthermore, the presence of myelin and neuronal antigens in functionally distinct APC populations within MS CLN suggests that differential immune responses can be evoked.

Indexed as

AnimalsAntigen-Presenting CellsAntigensBrainCallithrixEncephalomyelitis, Autoimmune, ExperimentalFemaleFlow CytometryFluorescent Antibody TechniqueGene ExpressionHumansImmunohistochemistryLymph NodesMacaca mulattaMacrophagesMaleAntigensCcr7 protein, mouseReceptors, CCR7

Identifiers

PMID19050840
OpenAlexW2124617804

What OpenQuestion holds

Textmetadata
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.