Evidence map›Paper›PMID 15784561›Full record

ArticleInfection and immunity2005

Effect of B7-2 and CD40 signals from activated antigen-presenting cells on the ability of zwitterionic polysaccharides to induce T-Cell stimulation.

Tom Li Stephen, Marcus Niemeyer, Arthur O Tzianabos, Martin Kroenke, Dennis L Kasper, Wiltrud M Kalka-Moll

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

17 citing papers in PubMed, 36 citations in OpenAlex.

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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

6 authors at 3 institutions in 2 countries.

Tom Li StephenInstitute for Medical Microbiology, Immunology and Hygiene, University of Cologne, Medical Center, Goldenfelsstr. 19-21, 50935 Cologne, Germany.
Marcus Niemeyer
Arthur O Tzianabos
Martin Kroenke
Dennis L Kasper
Wiltrud M Kalka-Moll
Institute of Medical Microbiology and Hygiene · DEBrigham and Women's Hospital · USHarvard University · US

Funding

PATHOGENIC MECHANISMS OF ANAEROBES IN SEPSISR01AI039576 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI KASPER, DENNIS L. · 1997 to 2007
$2.4M
PATHOGENIC MECHANISMS OF ANAEROBES IN SEPSISR21AI039576 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI KASPER, DENNIS L. · 1996 to 1996
–
BACTEROIDES FRAGILIS CAPSULES--SYNTHESIS AND VIRULENCER29AI034073 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI TZIANABOS, ARTHUR O · 1995 to 1999
–
NIAID NIH HHS AI 34073NIAID NIH HHS AI 39576NIAID NIH HHS R01 AI039576
6 · The paper itself

Abstract

Carbohydrates have been thought to stimulate immune responses independently of T cells; however, zwitterionic polysaccharides (ZPSs) from the capsules of some bacteria elicit potent CD4+-T-cell responses in vivo and in vitro. We demonstrated that HLA-DR on professional antigen-presenting cells (APCs) is required for ZPS-induced T-cell proliferation in vitro (15). Recently, it was shown that ZPSs are processed to low-molecular-weight carbohydrates by a nitric oxide-mediated mechanism in endosomes and locate in the major histocompatibility complex class II pathway (5, 15). The effect of the ZPS-mediated expression of HLA-DR and costimulatory molecules on the APC and T-cell engagement and subsequent T-cell activation has not been elucidated. Herein, we report that ZPS-mediated induction of HLA-DR-surface expression and T-cell proliferation are maximally enhanced after incubation of APCs for 8 h with ZPS. Treatment of APCs with bafilomycin A inhibits the up-regulation of ZPS-mediated HLA-DR surface expression and leads to inhibition of T-cell proliferation. Monoclonal antibodies (MAbs) to the costimulatory molecules B7-2 and CD40L specifically block ZPS-mediated T-cell activation, while a MAb to B7-1 does not. Surface expression of B7-2 and B7-1 but not of CD40 is maximally enhanced at 8 to 16 h of treatment of APCs with ZPS. The results demonstrate that the cellular immune response to ZPS depends on the translocation of HLA-DR to the cell surface and requires costimulation via B7-2 and CD40 on activated APCs. The implication is that activation of ZPS-specific T cells requires an orchestrated arrangement of both presenting and costimulatory molecules to form an immunological synapse.

Indexed as

Antigen-Presenting CellsAntigens, CDB7-2 AntigenCD28 AntigensCD40 AntigensCD40 LigandCells, CulturedHLA-DR AntigensHumansLymphocyte ActivationMembrane GlycoproteinsPolysaccharides, BacterialT-LymphocytesAntigens, CDB7-2 AntigenCD28 AntigensCD40 AntigensCD40 LigandCD86 protein, humanHLA-DR AntigensMembrane GlycoproteinsPolysaccharides, Bacterial

Identifiers

PMID15784561
PMCPMC1087428
OpenAlexW2095882994

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.