Evidence map›Paper›PMID 16552049›Full record

ArticleInfection and immunity2006

Antibody-independent, interleukin-17A-mediated, cross-serotype immunity to pneumococci in mice immunized intranasally with the cell wall polysaccharide.

Richard Malley, Amit Srivastava, Marc Lipsitch, Claudette M Thompson, Claire Watkins, Arthur Tzianabos, Porter W Anderson

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
10.5field-weighted citation impact, top 1% 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

91 citing papers in PubMed, 168 citations in OpenAlex.

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  13. Regenerative therapy based on miRNA-302 mimics for enhancing host recovery from pneumonia caused byProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
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  16. Mechanisms of Naturally Acquired Immunity toFrontiers in immunology · 2019
    Review
  17. Review
  18. Evaluation of the Role ofInfection and immunity · 2018
    Article
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31 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

7 authors at 4 institutions in 1 country.

Richard MalleyDivision of Infectious Diseases, Children's Hospital, 300 Longwood Avenue, Boston, MA 02115, USA. Richard.Malley@childrens.harvard.edu
Amit Srivastava
Marc Lipsitch
Claudette M Thompson
Claire Watkins
Arthur Tzianabos
Porter W Anderson
Harvard University · USBoston Children's Hospital · USBrigham and Women's Hospital · USUniversity of Rochester · US

Funding

INFECTIOUS DISEASE AND BASIC MICROBIOLOGICAL MECHANISMST32AI007061 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Marcia B Goldberg · 1985 to 2026
$12.1M
VACCINATION AND THE EVOLUTIONARY DYNAMICS OF PNEUMOCOCCIR01AI048935 · NIAID · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI LIPSITCH, MARC · 2001 to 2016
$8.8M
Pneumococcal immunization through a novel mechanismR01AI067737 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI MALLEY, RICHARD · 2006 to 2010
$2.0M
Pneumolysin, Innate and Acquired Immunity to PneumococciK08AI051526 · NIAID · CHILDREN'S HOSPITAL BOSTON · PI MALLEY, RICHARD · 2002 to 2005
$503k
NIAID NIH HHS 5R01 AI048935NIAID NIH HHS AI067737NIAID NIH HHS AI07061-26NIAID NIH HHS AI51526NIAID NIH HHS K08 AI051526NIAID NIH HHS R01 AI048935NIAID NIH HHS R01 AI067737NIAID NIH HHS T32 AI007061
6 · The paper itself

Abstract

Serotype-specific immunity to Streptococcus pneumoniae is conferred by antibodies to the capsular polysaccharides, which define the 90 known serotypes. Whether antibody to the species-common cell wall polysaccharide (C-Ps) is protective has been a matter of controversy. Here we show that C-Ps given intranasally with mucosal adjuvant increased the resistance of mice to experimental nasopharyngeal colonization by capsulated S. pneumoniae of serotype 6B. This immunity could be induced in mice congenitally lacking immunoglobulin but was dependent upon CD4+ T cells. Elimination of the charged amino group on the polymer backbone by N acetylation of C-Ps reduced the immunity, as did treatment of the mice with antibody to the cytokine interleukin-17A at the time of challenge, both consistent with the hypothesis of T-cell activation due to the zwitterionic motif of the polymer. C-Ps also protected in a model of fatal aspiration pneumonia by heavily capsulated serotype 3. These findings suggest a novel immunization strategy against S. pneumoniae.

Indexed as

Administration, IntranasalAnimalsAntibodies, BacterialAntigens, BacterialCD4-Positive T-LymphocytesCell WallImmunoglobulin GInterleukin-17MiceMice, Inbred C57BLMice, KnockoutMice, NudeNasopharyngeal DiseasesPneumococcal InfectionsPneumococcal VaccinesPneumonia, PneumococcalAntibodies, BacterialAntigens, BacterialImmunoglobulin GInterleukin-17Pneumococcal VaccinesPolysaccharides, BacterialProtein Subunits

Identifiers

PMID16552049
PMCPMC1418935
OpenAlexW2105668129

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.