Evidence map›Paper›PMID 31797910›Full record

ArticleMucosal immunology2020

Type I IFN ineffectively activates neonatal dendritic cells limiting respiratory antiviral T-cell responses.

Annie W Lau-Kilby, Mathilde Turfkruyer, Margaret Kehl, Lijuan Yang, Ursula J Buchholz, Kimberly Hickey, Allison M W Malloy

Open access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. 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

7 authors at 3 institutions in 1 country.

Annie W Lau-KilbyLaboratory of Infectious Diseases and Host Defense, Department of Pediatrics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA.
Mathilde TurfkruyerLaboratory of Infectious Diseases and Host Defense, Department of Pediatrics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA.
Margaret KehlLaboratory of Infectious Diseases and Host Defense, Department of Pediatrics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA.
Lijuan YangRNA Viruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bldg. 50, Rm 6503, 50 South Drive, MSC 8007, Bethesda, MD, 20892, USA.
Ursula J BuchholzRNA Viruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bldg. 50, Rm 6503, 50 South Drive, MSC 8007, Bethesda, MD, 20892, USA.
Kimberly HickeyDepartment of Obstetrics and Gynecology, Walter Reed National Military Medical Center, 8901 Wisconsin Avenue, Bethesda, MD, 20889, USA.
Allison M W MalloyLaboratory of Infectious Diseases and Host Defense, Department of Pediatrics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA. Allison.malloy@usuhs.edu.
Uniformed Services University of the Health Sciences · USNational Institutes of Health · USWalter Reed National Military Medical Center · US

Funding

Laboratory Studies of Human Respiratory Syncytial Virus and Other PneumovirusesZIAAI000372 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BUCHHOLZ, URSULA · 2009 to 2025
$21.8M
Respiratory mucosal immune development in early life and the quest for protective local memory against respiratory syncytial virus.R01AI154619 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI MALLOY, ALLISON MARIE WAHL · 2020 to 2023
$1.4M
Intramural NIH HHS Z99 AI999999NIAID NIH HHS R01 AI154619
6 · The paper itself

Abstract

Insufficient T-cell responses contribute to the increased burden of viral respiratory disease in infancy. Neonatal dendritic cells (DCs) often provide defective activation of pathogen-specific T cells through mechanisms that are incompletely understood, which hinders vaccine design for this vulnerable age group. Enhancing our characterization of neonatal DC sub-specialization and function is therefore critical to developing their potential for immunomodulation of T-cell responses. In this study, we engineered respiratory syncytial virus (RSV) to express a model protein, ovalbumin, to track antigen-presenting DCs in vivo. We found that murine neonatal conventional DC1s (cDC1s) efficiently migrated and presented RSV-derived antigen, challenging the paradigm that neonatal DCs are globally immature. In a key observation, however, we discovered that during infection neonatal cDC1s presenting viral antigen were unable to upregulate costimulatory molecules in response to type I interferons (IFN-I), contributing to poor antiviral T-cell responses. Importantly, we showed that the deficient response to IFN-I was also exhibited by human neonatal cDC1s, independent of infection. These findings reveal a functionally distinct response to IFN-I by neonatal cDC1s that may leave young infants susceptible to viral infections, and provide a new target for exploration, in light of failed efforts to design neonatal RSV vaccines.

Indexed as

Antigen PresentationAnimalsAnimals, NewbornCell DifferentiationCells, CulturedDendritic CellsFemaleHumansInfant, NewbornInfant, Newborn, DiseasesInterferon Type ILymphocyte ActivationMiceMice, Inbred BALB CMice, Inbred C57BLRespiratory Syncytial VirusesInterferon Type I

Identifiers

PMID31797910
PMCPMC7044048
OpenAlexW2993939126

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.