Evidence map›Paper›PMID 20308362›Full record

ArticleThe Journal of experimental medicine2010

Lymph node fibroblastic reticular cells directly present peripheral tissue antigen under steady-state and inflammatory conditions.

Anne L Fletcher, Veronika Lukacs-Kornek, Erika D Reynoso, Sophie E Pinner, Angelique Bellemare-Pelletier, Mark S Curry, Ai-Ris Collier, Richard L Boyd, Shannon J Turley

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 209 papers.

0numbers the graph read from it
0cells of the map it votes in
209citing papers in PubMed
–field-weighted citation impact
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

209 citing papers in PubMed.

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  15. Lymphatic transport in anti-tumor immunity and metastasis.The Journal of experimental medicine · 2025
    Review
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149 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Anne L FletcherDepartment of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Veronika Lukacs-Kornek
Erika D Reynoso
Sophie E Pinner
Angelique Bellemare-Pelletier
Mark S Curry
Ai-Ris Collier
Richard L Boyd
Shannon J Turley

Funding

TCR recognition of MHC class II peptide compexes in multiple sclerosisP01AI045757 · NIAID · DANA-FARBER CANCER INSTITUTE · PI KUCHROO, VIJAY K., LOVE, JOHN CHRISTOPHER · 1999 to 2017
$22.8M
Role of the gut epithelium in pancreatic autoimmunityR01DK074500 · NIDDK · DANA-FARBER CANCER INST · PI HAINING, WILLIAM NICHOLAS · 2007 to 2016
$3.4M
NIAID NIH HHS P01 AI045757NIDDK NIH HHS R01 DK074500
6 · The paper itself

Abstract

Lymph node stromal cells (LNSCs) can induce potent, antigen-specific T cell tolerance under steady-state conditions. Although expression of various peripheral tissue-restricted antigens (PTAs) and presentation to naive CD8+ T cells has been demonstrated, the stromal subsets responsible have not been identified. We report that fibroblastic reticular cells (FRCs), which reside in the T cell zone of the LN, ectopically express and directly present a model PTA to naive T cells, inducing their proliferation. However, we found that no single LNSC subset was responsible for PTA expression; rather, each subset had its own characteristic antigen display. Studies to date have concentrated on PTA presentation under steady-state conditions; however, because LNs are frequently inflammatory sites, we assessed whether inflammation altered stromal cell-T cell interactions. Strikingly, FRCs showed reduced stimulation of T cells after Toll-like receptor 3 ligation. We also characterize an LNSC subset expressing the highest levels of autoimmune regulator, which responds potently to bystander inflammation by up-regulating PTA expression. Collectively, these data show that diverse stromal cell types have evolved to constitutively express PTAs, and that exposure to viral products alters the interaction between T cells and LNSCs.

Indexed as

AnimalsAntigen PresentationAntigens, CDAutoantigensB7-1 AntigenB7-H1 AntigenCell ProliferationEndothelial CellsGene ExpressionHistocompatibility Antigens Class IImmune ToleranceImmunophenotypingInflammationLymph NodesLymphocyte ActivationMaleAntigens, CDAutoantigensB7-1 AntigenB7-H1 AntigenCd274 protein, mouseHistocompatibility Antigens Class IMembrane GlycoproteinsOvalbuminPeptidesPoly I-CTLR3 protein, mouseToll-Like Receptor 3

Identifiers

PMID20308362
PMCPMC2856033

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Registered trials

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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.