Evidence map›Paper›PMID 22914092›Full record

ArticleNature2012

T cells become licensed in the lung to enter the central nervous system.

Francesca Odoardi, Christopher Sie, Kristina Streyl, Vijay K Ulaganathan, Christian Schläger, Dmitri Lodygin, Klaus Heckelsmiller, Wilfried Nietfeld, Joachim Ellwart, Wolfgang E F Klinkert and 9 more

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In one paragraph

Article in Nature, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 243 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
243citing papers in PubMed, 2 pooled it
22.0field-weighted citation impact, top 1% 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

243 citing papers in PubMed, 2 syntheses or guidelines pooled it, 435 citations in OpenAlex.

  1. Pooled it
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  11. β-oxidation-mediated differentiation of effector CD4Journal of neuroinflammation · 2026
    Article
  12. Article
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  14. The role of NINJ1 in diseases.Cell death discovery · 2026
    Review
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183 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 8 institutions in 3 countries.

Francesca OdoardiInstitute for Multiple Sclerosis Research, Department of Neuroimmunology, Gemeinnützige Hertie-Stiftung and University Medical Centre Göttingen, 37073 Göttingen, Germany.
Christopher Sie
Kristina Streyl
Vijay K Ulaganathan
Christian Schläger
Dmitri Lodygin
Klaus Heckelsmiller
Wilfried Nietfeld
Joachim Ellwart
Wolfgang E F Klinkert
Claudio Lottaz
Mikhail Nosov
Volker Brinkmann
Rainer Spang
Hans Lehrach
Martin Vingron
Hartmut Wekerle
Cassandra Flügel-Koch
Alexander Flügel
Hertie Foundation · DEMax Planck Institute of Neurobiology · DEMax Planck Institute for Molecular Genetics · DEUniversity of Regensburg · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEHelmholtz Zentrum München · DENovartis Institutes for BioMedical ResearchOllscoil na Gaillimhe – University of Galway · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The blood–brain barrier (BBB) and the environment of the central nervous system (CNS) guard the nervous tissue from peripheral immune cells. In the autoimmune disease multiple sclerosis, myelin-reactive T-cell blasts are thought to transgress the BBB and create a pro-inflammatory environment in the CNS, thereby making possible a second autoimmune attack that starts from the leptomeningeal vessels and progresses into the parenchyma. Using a Lewis rat model of experimental autoimmune encephalomyelitis, we show here that contrary to the expectations of this concept, T-cell blasts do not efficiently enter the CNS and are not required to prepare the BBB for immune-cell recruitment. Instead, intravenously transferred T-cell blasts gain the capacity to enter the CNS after residing transiently within the lung tissues. Inside the lung tissues, they move along and within the airways to bronchus-associated lymphoid tissues and lung-draining mediastinal lymph nodes before they enter the blood circulation from where they reach the CNS. Effector T cells transferred directly into the airways showed a similar migratory pattern and retained their full pathogenicity. On their way the T cells fundamentally reprogrammed their gene-expression profile, characterized by downregulation of their activation program and upregulation of cellular locomotion molecules together with chemokine and adhesion receptors. The adhesion receptors include ninjurin 1, which participates in T-cell intravascular crawling on cerebral blood vessels. We detected that the lung constitutes a niche not only for activated T cells but also for resting myelin-reactive memory T cells. After local stimulation in the lung, these cells strongly proliferate and, after assuming migratory properties, enter the CNS and induce paralytic disease. The lung could therefore contribute to the activation of potentially autoaggressive T cells and their transition to a migratory mode as a prerequisite to entering their target tissues and inducing autoimmune disease.

Indexed as

Cell MovementAdoptive TransferAnimalsAutoimmunityBlood-Brain BarrierBrainCell Adhesion Molecules, NeuronalCerebrovascular CirculationDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalGene Expression ProfilingImmunologic MemoryLungLymphocyte ActivationMyelin SheathNerve Growth FactorsCell Adhesion Molecules, NeuronalNerve Growth FactorsNinj1 protein, rat

Identifiers

PMID22914092
OpenAlexW2166269696

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.