Evidence map›Paper›PMID 18778282›Full record

ArticleImmunology2009

Type I Streptococcus pneumoniae carbohydrate utilizes a nitric oxide and MHC II-dependent pathway for antigen presentation.

Christopher D Velez, Colleen J Lewis, Dennis L Kasper, Brian A Cobb

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

37 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. The Structural Complexity and Animal Tissue Distribution ofFrontiers in molecular biosciences · 2019
    Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

4 authors at 3 institutions in 1 country.

Christopher D VelezDepartment of Medicine, Channing Laboratory, Harvard Medical School, Boston, MA, USA.
Colleen J Lewis
Dennis L Kasper
Brian A Cobb
Harvard University · USCase Western Reserve University · USUniversity School · US

Funding

INFECTIOUS DISEASE AND BASIC MICROBIOLOGICAL MECHANISMST32AI007061 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Marcia B Goldberg · 1985 to 2026
$12.1M
PATHOGENIC MECHANISMS OF ANAEROBES IN SEPSISR01AI039576 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI KASPER, DENNIS L. · 1997 to 2007
$2.4M
T cell Dependent Immune Responses to Carbohydrate AntigensDP2OD004225 · OD · CASE WESTERN RESERVE UNIVERSITY · PI COBB, BRIAN A · 2008 to 2008
$1.9M
Biochemistry of Antigen Presentation MechanismsK22AI062707 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI COBB, BRIAN A · 2006 to 2007
$267k
PATHOGENIC MECHANISMS OF ANAEROBES IN SEPSISR21AI039576 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI KASPER, DENNIS L. · 1996 to 1996
–
NIAID NIH HHS AI039576NIAID NIH HHS AI062707NIAID NIH HHS K22 AI062707NIAID NIH HHS R01 AI039576NIAID NIH HHS T32 AI007061NIH HHS DP2 OD004225
6 · The paper itself

Abstract

Some pathogenic bacteria form thick capsules that both block immune responses through inhibition of complement deposition and phagocytosis and stimulate a weak response resulting from a lack of T-cell involvement. Contrary to this model, capsular polysaccharides from 23 serotypes of Streptococcus pneumoniae have been successfully used in a multivalent vaccine in the absence of a carrier protein. Furthermore, type I pneumococcal polysaccharide (Sp1) has been shown to activate T cells in vivo and in vitro via an uncharacterized mechanism. In the present report, we demonstrate that Sp1 utilizes the major histocompatibility complex (MHC) class II pathway in antigen-presenting cells (APCs) for processing and presentation. APCs internalize and process Sp1 through a nitric oxide-dependent mechanism and, once inside the cell, it associates with MHC II proteins in an H-2M-dependent manner that leads to in vivo T-cell activation. These results establish that Sp1 activates T cells which can lead to abscess formation in mice through an H-2M-dependent polysaccharide antigen presentation pathway in APCs, potentially contributing to pneumococcal polysaccharide vaccine efficacy through the recruitment of T-cell help.

Indexed as

AnimalsAntigen PresentationBinding, CompetitiveCells, CulturedEndosomesHistocompatibility Antigens Class IIHumansLymphocyte ActivationMiceMice, Inbred C57BLNitric OxideOxidation-ReductionPolysaccharides, BacterialSignal TransductionStreptococcus pneumoniaeTumor Cells, CulturedHistocompatibility Antigens Class IINitric Oxidepneumococcal polysaccharide type 1Polysaccharides, Bacterial

Identifiers

PMID18778282
PMCPMC2678183
OpenAlexW1593389290

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.