Evidence map›Paper›PMID 21074638›Full record

ReviewAgeing research reviews2011

Dysregulation of human Toll-like receptor function in aging.

Albert C Shaw, Alexander Panda, Samit R Joshi, Feng Qian, Heather G Allore, Ruth R Montgomery

Open access · greenAbstract readReview
In one paragraph

Review in Ageing research reviews, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 5% 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

106 citing papers in PubMed, 2 syntheses or guidelines pooled it, 212 citations in OpenAlex.

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  19. Host-Microbe Multiomic Profiling Reveals Age-Dependent COVID-19 Immunopathology.medRxiv : the preprint server for health sciences · 2024
    Article
  20. Article

46 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

6 authors at 1 institution in 1 country.

Albert C ShawSection of Infectious Diseases, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA. albert.shaw@yale.edu
Alexander Panda
Samit R Joshi
Feng Qian
Heather G Allore
Ruth R Montgomery
Yale University · US

Funding

Systems investigation of vaccine responses in B cell depleted autoimmune patientsU19AI089992 · NIAID · YALE UNIVERSITY · PI David A. Hafler, RUTH R MONTGOMERY · 2010 to 2026
$50.4M
Yale Study Support Suite (YES3): Dashboard and Web Portal Software Supporting Research Workflow through integrated, customizable REDCap External ModulesP30AG021342 · NIA · YALE UNIVERSITY · PI Denise Esserman · 2002 to 2026
$37.9M
BORRELIA BURGDORFERI INTERACTIONS WITH IXODES SCAPULARISR01AI032947 · NIAID · YALE UNIVERSITY · PI FIKRIG, EROL · 1998 to 2012
$5.1M
Interactions Between Anaplasma Phagocytophilum and Ixodes ScapularisR01AI041440 · NIAID · YALE UNIVERSITY · PI FIKRIG, EROL · 1998 to 2014
$5.0M
IMMUNE FUNCTION AND BIODEFENSE IN CHILDREN. ELDERLY AND IMMUNOCOMPROMI-266050031N01AI050031 · NIAID · EMORY UNIVERSITY · PI LARSEN, CHRISTOPHER · 2006 to 2006
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GENETICS OF REPRODUCTIVE LONGEVITY IN DROSOPHILAR01AG001934 · NIA · UNIVERSITY OF TEXAS AUSTIN · PI HIRAIZUMI, YUICHIRO · 1985 to 1987
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NIAID NIH HHS N01 AI050031NIAID NIH HHS N01 AI500031NIAID NIH HHS N01-AI-50031NIAID NIH HHS R01 AI032947NIAID NIH HHS R01 AI041440NIAID NIH HHS U19 AI089992NIAID NIH HHS U19-AI-089992NIA NIH HHS P30 AG021342NIA NIH HHS T32AG1934
6 · The paper itself

Abstract

Studies addressing immunosenescence in the immune system have expanded to focus on the innate as well as the adaptive responses. In particular, aging results in alterations in the function of Toll-like receptors (TLRs), the first described pattern recognition receptor family of the innate immune system. Recent studies have begun to elucidate the consequences of aging on TLR function in human cohorts and add to existing findings performed in animal models. In general, these studies show that human TLR function is impaired in the context of aging, and in addition there is evidence for inappropriate persistence of TLR activation in specific systems. These findings are consistent with an overarching theme of age-associated dysregulation of TLR signaling that likely contributes to the increased morbidity and mortality from infectious diseases found in geriatric patients.

Indexed as

AgedAged, 80 and overAgingDendritic CellsHumansImmunity, InnateMacrophagesSignal TransductionToll-Like ReceptorsToll-Like Receptors

Identifiers

PMID21074638
PMCPMC3633557
OpenAlexW1968377406

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.