Evidence map›Paper›PMID 20102413›Full record

ArticleImmunology2010

Differences in innate immune responses correlate with differences in murine susceptibility to Chlamydia muridarum pulmonary infection.

Xiaozhou Jiang, Caixia Shen, Hong Yu, Karuna P Karunakaran, Robert C Brunham

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Article
  3. Identification of KeyInternational journal of molecular sciences · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Immunogenicity of Protein Pharmaceuticals.Journal of pharmaceutical sciences · 2019
    Review
  12. Article
  13. Article
  14. Article
  15. TheFrontiers in microbiology · 2017
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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

5 authors at 2 institutions in 1 country.

Xiaozhou JiangBritish Columbia Centre for Disease Control, University of British Columbia, Vancouver, BC, Canada.
Caixia Shen
Hong Yu
Karuna P Karunakaran
Robert C Brunham
University of British Columbia · CABC Centre for Disease Control · CA

Funding

Development of a Chlamydia T Cell Vaccine Based on Dendritic Cell ImmunoprotemicsR01AI076483 · NIAID · UNIVERSITY OF BRITISH COLUMBIA · PI BRUNHAM, ROBERT CONRAD, FOSTER, LEONARD J · 2008 to 2012
$1.1M
NIAID NIH HHS R01 AI076483NIAID NIH HHS R01AI076483
6 · The paper itself

Abstract

We investigated the phenotypic basis for genetically determined differences in susceptibility and resistance to Chlamydia muridarum pulmonary infection using BALB/c and C57BL/6 mice. Following C. muridarum intranasal inoculation, the intensity of infection was very different between BALB/c and C57BL/6 beginning as early as 3 days post-infection. Intrapulmonary cytokine patterns also differed at early time-points (days 2 and 4) between these two strains of mice. The early recruitment of neutrophils to lung tissue was greater in BALB/c than in C57BL/6 mice and correlated with a higher number of inclusion forming units (IFU) of C. muridarum. At day 12 post-infection, BALB/c mice continued to demonstrate a greater burden of infection, significantly higher lung cytokine levels for tumour necrosis factor-alpha and interleukin-17 (IL-17) and a significantly lower level for interferon-gamma than did C57BL/6 mice. In vitro, bone-marrow-derived dendritic cells (BMDCs) from BALB/c mice underwent less functional maturation in response to C. muridarum infection than did BMDCs from C57BL/6 mice. The BMDCs of BALB/c mice expressed lower levels of activation markers (CD80, CD86, CD40 and major histocompatibility complex class II) and secreted less IL-12 and more IL-23 than BMDCs from C57BL/6 mice. Overall, the data demonstrate that the differences exhibited by BALB/c and C57BL/6 mice following C. muridarum pulmonary infection are associated with differences in early innate cytokine and cellular responses that are correlated with late differences in T helper type 17 versus type 1 adaptive immune responses.

Indexed as

AnimalsChlamydia InfectionsChlamydia muridarumCytokinesDisease Models, AnimalDisease SusceptibilityFemaleHeLa CellsHumansImmunity, InnateInterleukin-17MiceMice, Inbred BALB CMice, Inbred C57BLPhenotypePneumonia, BacterialCytokinesInterleukin-17

Identifiers

PMID20102413
PMCPMC2842502
OpenAlexW1547987574

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.