Evidence map›Paper›PMID 22792067›Full record

ArticlePLoS pathogens2012

The lectin pathway of complement activation is a critical component of the innate immune response to pneumococcal infection.

Youssif M Ali, Nicholas J Lynch, Kashif S Haleem, Teizo Fujita, Yuichi Endo, Soren Hansen, Uffe Holmskov, Kazue Takahashi, Gregory L Stahl, Thomas Dudler and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed, 1 pooled it
6.9field-weighted citation impact, top 2% 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

83 citing papers in PubMed, 1 synthesis or guideline pooled it, 163 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. The Role of Ficolins in Lung Injury.Journal of innate immunity · 2024
    Review
  11. Article
  12. Article
  13. Review
  14. Frontiers in cellular and infection microbiology · 2022
    Review
  15. Article
  16. Article
  17. Protective role of host complement system inFrontiers in immunology · 2022
    Article
  18. Article
  19. Activity of Mannose-Binding Lectin on Bacterial-Infected Chickens-A Review.Animals : an open access journal from MDPI · 2021
    Review
  20. Review

23 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

16 authors at 5 institutions in 5 countries.

Youssif M AliDepartment of Infection, Immunity and Inflammation, University of Leicester, Leicester, United Kingdom.
Nicholas J Lynch
Kashif S Haleem
Teizo Fujita
Yuichi Endo
Soren Hansen
Uffe Holmskov
Kazue Takahashi
Gregory L Stahl
Thomas Dudler
Umakhanth V Girija
Russell Wallis
Aras Kadioglu
Cordula M Stover
Peter W Andrew
Wilhelm J Schwaeble
University of Leicester · GBFukushima Medical University · JPHarvard University · USUniversity of Southern Denmark · DKOmeros Corporation (United States) · US

Funding

Medical Research Council G0801952Medical Research Council G1000191
6 · The paper itself

Abstract

The complement system plays a key role in host defense against pneumococcal infection. Three different pathways, the classical, alternative and lectin pathways, mediate complement activation. While there is limited information available on the roles of the classical and the alternative activation pathways of complement in fighting streptococcal infection, little is known about the role of the lectin pathway, mainly due to the lack of appropriate experimental models of lectin pathway deficiency. We have recently established a mouse strain deficient of the lectin pathway effector enzyme mannan-binding lectin associated serine protease-2 (MASP-2) and shown that this mouse strain is unable to form the lectin pathway specific C3 and C5 convertases. Here we report that MASP-2 deficient mice (which can still activate complement via the classical pathway and the alternative pathway) are highly susceptible to pneumococcal infection and fail to opsonize Streptococcus pneumoniae in the none-immune host. This defect in complement opsonisation severely compromises pathogen clearance in the lectin pathway deficient host. Using sera from mice and humans with defined complement deficiencies, we demonstrate that mouse ficolin A, human L-ficolin, and collectin 11 in both species, but not mannan-binding lectin (MBL), are the pattern recognition molecules that drive lectin pathway activation on the surface of S. pneumoniae. We further show that pneumococcal opsonisation via the lectin pathway can proceed in the absence of C4. This study corroborates the essential function of MASP-2 in the lectin pathway and highlights the importance of MBL-independent lectin pathway activation in the host defense against pneumococci.

Indexed as

Complement ActivationImmunity, InnateAnimalsCollectinsComplement C4FicolinsHumansLectinsMannose-Binding LectinMannose-Binding Protein-Associated Serine ProteasesMiceMice, Inbred C57BLMice, KnockoutOpsonin ProteinsPneumococcal InfectionsReceptors, Pattern RecognitionCollectinsComplement C4FicolinsLectinsMannose-Binding LectinMannose-Binding Protein-Associated Serine ProteasesMASP-2 protein, mouseOpsonin ProteinsReceptors, Pattern Recognition

Identifiers

PMID22792067
PMCPMC3390405
OpenAlexW2170658957

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.