Evidence map›Paper›PMID 20154206›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

Characterizing the dynamics of CD4+ T cell priming within a lymph node.

Jennifer J Linderman, Thomas Riggs, Manjusha Pande, Mark Miller, Simeone Marino, Denise E Kirschner

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

43 citing papers in PubMed, 63 citations in OpenAlex.

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  19. Agent-based models of inflammation in translational systems biology: A decade later.Wiley interdisciplinary reviews. Systems biology and medicine · 2019
    Review
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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.

Jennifer J LindermanDepartment of Chemical Engineering, Center for Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109, USA.
Thomas Riggs
Manjusha Pande
Mark Miller
Simeone Marino
Denise E Kirschner
University of Michigan · USInstitute of Bioinformatics · INWashington University in St. Louis · US

Funding

Modeling Immunity for BiodefenseN01AI50018 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STEINMETZ, KAREN · 2008 to 2011
$3.5M
Chemokine Dynamics in the HIV-1/SIV Infected LungR01HL072682 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KIRSCHNER, DENISE E · 2002 to 2006
$2.6M
The dynamics of granuloma formation in tuberculosisR01HL068526 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KIRSCHNER, DENISE E · 2001 to 2005
$2.3M
"MSM" A multi-scale approach for understanding antigen presentation in immunityR01LM009027 · NLM · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KIRSCHNER, DENISE E · 2005 to 2007
$1.1M
A multi-scale and multi-system approach to understand granuloma formation in TBR33HL092853 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KIRSCHNER, DENISE E · 2008 to 2010
$684k
A multi-scale and multi-system approach to understand granuloma formation in TBR33HL092844 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LINDERMAN, JENNIFER JEAN · 2008 to 2010
$656k
NHLBI NIH HHS HL092844NHLBI NIH HHS HL092853NHLBI NIH HHS HL68526NHLBI NIH HHS HL72682NHLBI NIH HHS R01 HL068526NHLBI NIH HHS R01 HL072682NHLBI NIH HHS R33 HL092844NHLBI NIH HHS R33 HL092853NIAID NIH HHS N01 AI050018NIAID NIH HHS N01 AI50018NLM NIH HHS LM00902701NLM NIH HHS R01 LM009027
6 · The paper itself

Abstract

Generating adaptive immunity postinfection or immunization requires physical interaction within a lymph node T zone between Ag-bearing dendritic cells (DCs) and rare cognate T cells. Many fundamental questions remain regarding the dynamics of DC-CD4+ T cell interactions leading to priming. For example, it is not known how the production of primed CD4+ T cells relates to the numbers of cognate T cells, Ag-bearing DCs, or peptide-MHCII level on the DC. To address these questions, we developed an agent-based model of a lymph node to examine the relationships among cognate T cell frequency, DC density, parameters characterizing DC-T cell interactions, and the output of primed T cells. We found that the output of primed CD4+ T cells is linearly related to cognate frequency, but nonlinearly related to the number of Ag-bearing DCs present during infection. This addresses the applicability of two photon microscopy studies to understanding actual infection dynamics, because these types of experiments increase the cognate frequency by orders of magnitude compared with physiologic levels. We found a trade-off between the quantity of peptide-major histocompatibility class II on the surface of individual DCs and number of Ag-bearing DCs present in the lymph node in contributing to the production of primed CD4+ T cells. Interestingly, peptide-major histocompatibility class II t(1/2) plays a minor, although still significant, role in determining CD4+ T cell priming, unlike the primary role that has been suggested for CD8+ T cell priming. Finally, we identify several pathogen-targeted mechanisms that, if altered in their efficiency, can significantly effect the generation of primed CD4+ T cells.

Indexed as

Computer SimulationModels, ImmunologicalMolecular Dynamics SimulationAdaptive ImmunityAnimalsAntibodiesAntigensBacterial InfectionsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell AdhesionCell CommunicationCell MovementDendritic CellsEndothelium, LymphaticLymph NodesAntibodiesAntigens

Identifiers

PMID20154206
PMCPMC3153313
OpenAlexW2142603939

What OpenQuestion holds

Textmetadata
LicenceTDM
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.