Evidence map›Paper›PMID 19917677›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

Neonatal innate TLR-mediated responses are distinct from those of adults.

Tobias R Kollmann, Juliet Crabtree, Annie Rein-Weston, Darren Blimkie, Francis Thommai, Xiu Yu Wang, Pascal M Lavoie, Jeff Furlong, Edgardo S Fortuno, Adeline M Hajjar and 3 more

Registry-linked trialAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02554630 (Novel Mechanisms and Approaches to Treat Neonatal Sepsis), which is not on this map. Cited by 287 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
287citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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.

NCT02554630 completednot on this mapstarted 2016, after this paper: background citation

Novel Mechanisms and Approaches to Treat Neonatal Sepsis: Adjuvant Therapies, Host Microbiome, and Genomic Expression and Functional Capacity of Innate Immune Cells

TypeobservationalSponsorUniversity of FloridaRan2016 to 2022Enrolled142ConditionsComplication of Prematurity, Immunologic Deficiency SyndromesArmsAdjuvant, Blood Collection
3 · Its place in the literature

Who cites it

287 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. A Balanced Proinflammatory and Regulatory Cytokine Signature in Young African Children Is Associated With Lower Risk of Clinical Malaria.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2019
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  8. Myeloid TLR2 signaling amplifies immunopathology in influenza-infected murine neonates.American journal of respiratory cell and molecular biology · 2026
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227 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

13 authors.

Tobias R KollmannDivision of Infectious and Immunological Diseases, Department of Pediatrics, University of British Columbia, CFRI, 950 West 28th Avenue, Vancouver, BC, V5Z4H4, Canada. tkollm@mac.com
Juliet Crabtree
Annie Rein-Weston
Darren Blimkie
Francis Thommai
Xiu Yu Wang
Pascal M Lavoie
Jeff Furlong
Edgardo S Fortuno
Adeline M Hajjar
Natalie R Hawkins
Steven G Self
Christopher B Wilson

Funding

IMMUNE FUNCTION AND BIODEFENSE IN CHILDREN. ELDERLY AND IMMUNOCOMPROMI-266050023N01AI050023 · NIAID · UNIVERSITY OF WASHINGTON · PI WILSON, CHRISTOPHER · 2006 to 2006
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CIHR 94325-1NIAID NIH HHS N01 AI050023
6 · The paper itself

Abstract

The human neonate and infant are unduly susceptible to infection with a wide variety of microbes. This susceptibility is thought to reflect differences from adults in innate and adaptive immunity, but the nature of these differences is incompletely characterized. The innate immune response directs the subsequent adaptive immune response after integrating information from TLRs and other environmental sensors. We set out to provide a comprehensive analysis defining differences in response to TLR ligation between human neonates and adults. In response to most TLR ligands, neonatal innate immune cells, including monocytes and conventional and plasmacytoid dendritic cells produced less IL-12p70 and IFN-alpha (and consequently induced less IFN-gamma), moderately less TNF-alpha, but as much or even more IL-1beta, IL-6, IL-23, and IL-10 than adult cells. At the single-cell level, neonatal innate cells generally were less capable of producing multiple cytokines simultaneously, i.e., were less polyfunctional. Overall, our data suggest a robust if not enhanced capacity of the neonate vs the adult white-blood cell TLR-mediated response to support Th17- and Th2-type immunity, which promotes defense against extracellular pathogens, but a reduced capacity to support Th1-type responses, which promote defense against intracellular pathogens.

Indexed as

AdultCytokinesDendritic CellsEnzyme-Linked Immunosorbent AssayFlow CytometryHumansImmunity, InnateInfantInfant, NewbornMonocytesToll-Like ReceptorsCytokinesToll-Like Receptors

Identifiers

PMID19917677
PMCPMC4556237

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.