Evidence map›Paper›PMID 15882345›Full record

ReviewImmunological reviews2005

Immunosenescence and macrophage functional plasticity: dysregulation of macrophage function by age-associated microenvironmental changes.

Robert D Stout, Jill Suttles

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

105 citing papers in PubMed, 219 citations in OpenAlex.

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  16. Prenylated Dihydroflavonol fromMolecules (Basel, Switzerland) · 2024
    Article
  17. Article
  18. Factors affecting the sensitivity of quantitative severe acute respiratory syndrome coronavirus 2 antigen test.Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy · 2023
    Article
  19. Review
  20. Review

45 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Robert D StoutDepartment of Microbiology and Immunology, University of Louisville School of Medicine, KY 40292, USA. bobstout@louisville.edu
Jill Suttles
University of Louisville · US

Funding

Fatty Acid Binding Proteins in Macrophage FunctionR01AI048850 · NIAID · UNIVERSITY OF LOUISVILLE · PI SUTTLES, JILL · 2003 to 2013
$3.2M
Macrophage Dysfunction in ImmunosenescenceR01AG020972 · NIA · UNIVERSITY OF LOUISVILLE · PI STOUT, ROBERT D · 2003 to 2006
$1.2M
NIAID NIH HHS R01 AI048850-01A2NIA NIH HHS R01 AG020972-01A1NIA NIH HHS R01 AG020972-02NIA NIH HHS R01 AG020972-03
6 · The paper itself

Abstract

The macrophage lineage displays extreme functional and phenotypic heterogeneity, which appears to be because, in large part, of the ability of macrophages to functionally adapt to changes in their tissue microenvironment. This functional plasticity of macrophages plays a critical role in their ability to respond to tissue damage and/or infection and to contribute to clearance of damaged tissue and invading microorganisms, to recruitment of the adaptive immune system, and to resolution of the wound and of the immune response. Evidence has accumulated that environmental influences, such as stromal function and imbalances in hormones and cytokines, contribute significantly to the dysfunction of the adaptive immune system. The innate immune system also appears to be dysfunctional in aged animals and humans. In this review, the hypothesis is presented and discussed that the observed age-associated 'dysfunction' of macrophages is the result of their functional adaptation to the age-associated changes in tissue environments. The resultant loss of orchestration of the manifold functional capabilities of macrophages would undermine the efficacy of both the innate and adaptive immune systems. The macrophages appear to maintain functional plasticity during this dysregulation, making them a prime target of cytokine therapy that could enhance both innate and adaptive immune systems.

Indexed as

AgingAnimalsCell LineageHumansImmune SystemMacrophagesSignal Transduction

Identifiers

PMID15882345
PMCPMC1201508
OpenAlexW2145034018

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.