Evidence map›Paper›PMID 18353940›Full record

ArticleJournal of virology2008

Differential response of respiratory dendritic cell subsets to influenza virus infection.

Xueli Hao, Taeg S Kim, Thomas J Braciale

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

75 citing papers in PubMed, 114 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Antiviral Approaches against Influenza Virus.Clinical microbiology reviews · 2023
    Review
  5. Review
  6. Antigen Presentation in the Lung.Frontiers in immunology · 2022
    Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

15 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

3 authors at 2 institutions in 1 country.

Xueli HaoCarter Immunology Center, UVA, P.O. Box 801386, Charlottesville, VA 22908, USA.
Taeg S Kim
Thomas J Braciale
Carter Center · USUniversity of Virginia · US

Funding

Vaccine strategy for broad spectrum protection agains non-typhoidal salmonellU54AI057168 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI CROSS, ALAN S. · 2003 to 2013
$91.5M
CYTOTOXIC T LYMPHOCYTE RESPONSE TO INFLUENZA VIRUSR01AI015608 · NIAID · WASHINGTON UNIVERSITY · PI BRACIALE, THOMAS J · 1985 to 2017
$5.7M
T Cell Function in Pulmonary Viral Pulmonary Infection and InjuryR01HL033391 · NHLBI · WASHINGTON UNIVERSITY · PI BRACIALE, THOMAS J · 1985 to 2012
$4.3M
IMMUNOBIOLOGY OF EXPERIMENTAL RSV INFECTIONR01AI037293 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI BRACIALE, THOMAS J · 1994 to 2007
$2.3M
CYTOTOXIC T LYMPHOCYTE RESPONSE TO INFLUENZA VIRUSR37AI015608 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI BRACIALE, THOMAS J · 1991 to 2000
$334k
NHLBI NIH HHS HL-33391NHLBI NIH HHS R01 HL033391NIAID NIH HHS AI-15608NIAID NIH HHS AI-37293NIAID NIH HHS AI-57168NIAID NIH HHS R01 AI015608NIAID NIH HHS R01 AI037293NIAID NIH HHS R37 AI015608NIAID NIH HHS U54 AI057168
6 · The paper itself

Abstract

Dendritic cells (DC) are believed to play an important role in the initiation of innate and adaptive immune responses to infection, including respiratory tract infections, where respiratory DC (RDC) perform this role. In this report, we examined the susceptibilities of isolated murine RDC to influenza virus infection in vitro and the effect of the multiplicity of infection (MOI) on costimulatory ligand upregulation and inflammatory cytokine/chemokine production after infection. We found that the efficiency of influenza virus infection of RDC increased with increasing MOIs. Furthermore, distinct subpopulations of RDC differed in their susceptibilities to influenza virus infection and in the magnitude/tempo of costimulatory ligand expression. Additional characterization of the CD11c-positive (CD11c(+)) RDC revealed that the identifiable subsets of RDC differed in susceptibility to infection, with CD11c(+) CD103(+) DC exhibiting the greatest susceptibility, CD11c(+) CD11b(hi) DC exhibiting intermediate susceptibility, and CD11c(+) B220(+) plasmacytoid DC (pDC) exhibiting the least susceptibility to infection. A companion analysis of the in vivo susceptibilities of these RDC subsets to influenza virus revealed a corresponding infection pattern. The three RDC subsets displayed different patterns of cytokine/chemokine production in response to influenza virus infection in vitro: pDC were the predominant producers of most cytokines examined, while CD103(+) DC and CD11b(hi) DC produced elevated levels of the murine chemokine CXCL1 (KC), interleukin 12p40, and RANTES in response to influenza virus infection. Our results indicate that RDC are targets of influenza virus infection and that distinct RDC subsets differ in their susceptibilities and responses to infection.

Indexed as

AnimalsAntigens, CDCD11b AntigenCD11c AntigenCytokinesDendritic CellsFemaleFlow CytometryInfluenza A Virus, H2N2 SubtypeIntegrin alpha ChainsLeukocyte Common AntigensMiceMice, Inbred BALB COrthomyxoviridae InfectionsRespiratory Systemalpha E integrinsAntigens, CDCD11b AntigenCD11c AntigenCytokinesIntegrin alpha ChainsLeukocyte Common Antigens

Identifiers

PMID18353940
PMCPMC2346724
OpenAlexW2129630141

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.