Evidence map›Paper›PMID 18802458›Full record

ArticlePLoS pathogens2008

Interleukin-17A mediates acquired immunity to pneumococcal colonization.

Ying-Jie Lu, Jane Gross, Debby Bogaert, Adam Finn, Linda Bagrade, Qibo Zhang, Jay K Kolls, Amit Srivastava, Anna Lundgren, Sophie Forte and 5 more

Abstract read
In one paragraph

Article in PLoS pathogens, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 274 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
274citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

274 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  6. Effect of age and vaccination with a pneumococcal conjugate vaccine on the density of pneumococcal nasopharyngeal carriage.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2012
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214 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

15 authors.

Ying-Jie LuDepartment of Medicine, Division of Infectious Diseases, Children's Hospital, and Harvard Medical School, Boston, Massachusetts, United States of America.
Jane Gross
Debby Bogaert
Adam Finn
Linda Bagrade
Qibo Zhang
Jay K Kolls
Amit Srivastava
Anna Lundgren
Sophie Forte
Claudette M Thompson
Kathleen F Harney
Porter W Anderson
Marc Lipsitch
Richard Malley

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 AI067737-01NIAID NIH HHS AI51526-01NIAID NIH HHS K08 AI051526NIAID NIH HHS R01 AI048935NIAID NIH HHS R01 AI067737NIAID NIH HHS T32 AI007061
6 · The paper itself

Abstract

Although anticapsular antibodies confer serotype-specific immunity to pneumococci, children increase their ability to clear colonization before these antibodies appear, suggesting involvement of other mechanisms. We previously reported that intranasal immunization of mice with pneumococci confers CD4+ T cell-dependent, antibody- and serotype-independent protection against colonization. Here we show that this immunity, rather than preventing initiation of carriage, accelerates clearance over several days, accompanied by neutrophilic infiltration of the nasopharyngeal mucosa. Adoptive transfer of immune CD4+ T cells was sufficient to confer immunity to naïve RAG1(-/-) mice. A critical role of interleukin (IL)-17A was demonstrated: mice lacking interferon-gamma or IL-4 were protected, but not mice lacking IL-17A receptor or mice with neutrophil depletion. In vitro expression of IL-17A in response to pneumococci was assayed: lymphoid tissue from vaccinated mice expressed significantly more IL-17A than controls, and IL-17A expression from peripheral blood samples from immunized mice predicted protection in vivo. IL-17A was elicited by pneumococcal stimulation of tonsillar cells of children or adult blood but not cord blood. IL-17A increased pneumococcal killing by human neutrophils both in the absence and in the presence of antibodies and complement. We conclude that IL-17A mediates pneumococcal immunity in mice and probably in humans; its elicitation in vitro could help in the development of candidate pneumococcal vaccines.

Indexed as

Adoptive TransferAdultAnimalsCD4-Positive T-LymphocytesChildFemaleHumansImmunityInterleukin-17MiceMice, Inbred C57BLNeutrophilsPneumococcal InfectionsStreptococcus pneumoniaeInterleukin-17

Identifiers

PMID18802458
PMCPMC2528945

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.