Evidence map›Paper›PMID 21798267›Full record

ReviewJournal of theoretical biology2011

Systems biology approaches for understanding cellular mechanisms of immunity in lymph nodes during infection.

Henry P Mirsky, Mark J Miller, Jennifer J Linderman, Denise E Kirschner

Open access · greenAbstract readReview
In one paragraph

Review in Journal of theoretical biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Dynamic multispectral NIR/SWIR forJournal of biomedical optics · 2024
    Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
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  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Agent-Based Modeling in Systems Pharmacology.CPT: pharmacometrics & systems pharmacology · 2015
    Article
  18. Modeling the T cell immune response: a fascinating challenge.Journal of pharmacokinetics and pharmacodynamics · 2014
    Review
  19. Article
  20. Article
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

4 authors at 2 institutions in 1 country.

Henry P MirskyDepartment of Chemical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.
Mark J Miller
Jennifer J Linderman
Denise E Kirschner
University of Michigan–Ann Arbor · USWashington University in St. Louis · US

Funding

Predicting immune responses that correlate with protection against tuberculosisR01HL110811 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FLYNN, JOANNE L., KIRSCHNER, DENISE E · 2012 to 2016
$5.9M
Epithelial Responses to Bacterial InvasionR01AI077600 · NIAID · WASHINGTON UNIVERSITY · PI MILLER, MARK JAMES · 2009 to 2021
$3.8M
Defining how the spectrum of latency affects reactivation of TBR01HL106804 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FLYNN, JOANNE L., KIRSCHNER, DENISE E · 2010 to 2013
$2.6M
A multi-scale model to predict outcomes of immunomodulation and drug therapy duriR01EB012579 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FLYNN, JOANNE L., KIRSCHNER, DENISE E · 2011 to 2014
$2.3M
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 R01 HL106804NHLBI NIH HHS R01HL106804NHLBI NIH HHS R01 HL110811NHLBI NIH HHS R33 HL092844NHLBI NIH HHS R33HL092844NHLBI NIH HHS R33 HL092853NHLBI NIH HHS R33HL092853NIAID NIH HHS R01 AI077600NIBIB NIH HHS R01 EB012579
6 · The paper itself

Abstract

Adaptive immunity is initiated in secondary lymphoid tissues when naive T cells recognize foreign antigen presented as MHC-bound peptide on the surface of dendritic cells. Only a small fraction of T cells in the naive repertoire will express T cell receptors specific for a given epitope, but antigen recognition triggers T cell activation and proliferation, thus greatly expanding antigen-specific clones. Expanded T cells can serve a helper function for B cell responses or traffic to sites of infection to secrete cytokines or kill infected cells. Over the past decade, two-photon microscopy of lymphoid tissues has shed important light on T cell development, antigen recognition, cell trafficking and effector functions. These data have enabled the development of sophisticated quantitative and computational models that, in turn, have been used to test hypotheses in silico that would otherwise be impossible or difficult to explore experimentally. Here, we review these models and their principal findings and highlight remaining questions where modeling approaches are poised to advance our understanding of complex immunological systems.

Indexed as

Models, ImmunologicalAdaptive ImmunityAnimalsCommunicable DiseasesDendritic CellsHumansLymph NodesSystems BiologyT-Lymphocytes

Identifiers

PMID21798267
PMCPMC4504675
OpenAlexW2069858587

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.