Evidence map›Paper›PMID 34845729›Full record

ReviewImmunological reviews2022

Information flow in the spatiotemporal organization of immune responses.

Jessica Y Huang, Miranda R Lyons-Cohen, Michael Y Gerner

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. PI16Nature immunology · 2023
    Article
  11. Article
  12. Review
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

3 authors at 1 institution in 1 country.

Jessica Y HuangDepartment of Immunology, University of Washington, Seattle, Washington, USA.
Miranda R Lyons-CohenDepartment of Immunology, University of Washington, Seattle, Washington, USA.
Michael Y GernerDepartment of Immunology, University of Washington, Seattle, Washington, USA.ORCID 0000-0001-5406-8308
University of Washington · US

Funding

TRAINING IN MOLECULAR AND CELLULAR BIOLOGYT32GM007270 · NIGMS · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2020
$21.0M
The Roles of Lymphoid Tissue Microenvironments in Guiding the Immune ResponseR01AI134713 · NIAID · UNIVERSITY OF WASHINGTON · PI Michael Gerner · 2018 to 2026
$4.4M
Novel approaches to study the intersection of cellular heterogeneity and tissue microanatomyR21AI142667 · NIAID · UNIVERSITY OF WASHINGTON · PI GERNER, MICHAEL · 2019 to 2020
$485k
Regulation of monocyte trafficking into lymph nodes during inflammationF31AI161316 · NIAID · UNIVERSITY OF WASHINGTON · PI HUANG, JESSICA · 2021 to 2023
$140k
NIAID NIH HHS F31 AI161316NIAID NIH HHS R01 AI134713NIAID NIH HHS R21 AI142667NIGMS NIH HHS T32 GM007270
6 · The paper itself

Abstract

Immune responses must be rapid, tightly orchestrated, and tailored to the encountered stimulus. Lymphatic vessels facilitate this process by continuously collecting immunological information (ie, antigens, immune cells, and soluble mediators) about the current state of peripheral tissues, and transporting these via the lymph across the lymphatic system. Lymph nodes (LNs), which are critical meeting points for innate and adaptive immune cells, are strategically located along the lymphatic network to intercept this information. Within LNs, immune cells are spatially organized, allowing them to efficiently respond to information delivered by the lymph, and to either promote immune homeostasis or mount protective immune responses. These responses involve the activation and functional cooperation of multiple distinct cell types and are tailored to the specific inflammatory conditions. The natural patterns of lymph flow can also generate spatial gradients of antigens and agonists within draining LNs, which can in turn further regulate innate cell function and localization, as well as the downstream generation of adaptive immunity. In this review, we explore how information transmitted by the lymph shapes the spatiotemporal organization of innate and adaptive immune responses in LNs, with particular focus on steady state and Type-I vs. Type-II inflammation.

Indexed as

Adaptive ImmunityDendritic CellsAntigensCell MovementHumansInflammationLymph NodesAntigensdendritic cellsinflammationin vivo imaginglymph nodesmonocytes/macrophagesT cells

Identifiers

PMID34845729
PMCPMC8837692
OpenAlexW3216011372

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.