Evidence map›Paper›PMID 25512603›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

The α-tocopherol form of vitamin E reverses age-associated susceptibility to streptococcus pneumoniae lung infection by modulating pulmonary neutrophil recruitment.

Elsa N Bou Ghanem, Stacie Clark, Xiaogang Du, Dayong Wu, Andrew Camilli, John M Leong, Simin N Meydani

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 92 citations in OpenAlex.

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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 3 institutions in 1 country.

Elsa N Bou GhanemDepartment of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, MA 02111;
Stacie ClarkDepartment of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, MA 02111;
Xiaogang DuJean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston MA 02114; and.
Dayong WuJean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston MA 02114; and.
Andrew CamilliDepartment of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, MA 02111; Howard Hughes Medical Institute, Boston, MA 02111.
John M LeongDepartment of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, MA 02111; simin.meydani@tufts.edu john.leong@tufts.edu.
Simin N MeydaniJean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston MA 02114; and simin.meydani@tufts.edu john.leong@tufts.edu.
Tufts University · USHoward Hughes Medical Institute · USJean Mayer Human Nutrition Research Center on Aging · US

Funding

STRUCTURE-FUNCTION RELATIONSHIPS IN THE ALIMENTARY TRACTP30DK034854 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WAYNE I LENCER · 1986 to 2026
$32.4M
Howard Hughes Medical InstituteNIDDK NIH HHS P30 DK034854
6 · The paper itself

Abstract

Streptococcus pneumoniae infections are an important cause of morbidity and mortality in older patients. Uncontrolled neutrophil-driven pulmonary inflammation exacerbates this disease. To test whether the α-tocopherol (α-Toc) form of vitamin E, a regulator of immunity, can modulate neutrophil responses as a preventive strategy to mitigate the age-associated decline in resistance to S. pneumoniae, young (4 mo) and old (22-24 mo) C57BL/6 mice were fed a diet containing 30-PPM (control) or 500-PPM (supplemented) α-Toc for 4 wk and intratracheally infected with S. pneumoniae. Aged mice fed a control diet were exquisitely more susceptible to S. pneumoniae than young mice. At 2 d postinfection, aged mice suffered 1000-fold higher pulmonary bacterial burden, 2.2-fold higher levels of neutrophil recruitment to the lung, and a 2.25-fold higher rate of lethal septicemia. Strikingly, α-Toc supplementation of aged mice resulted in a 1000-fold lower bacterial lung burden and full control of infection. This α-Toc-induced resistance to pneumococcal challenge was associated with a 2-fold fewer pulmonary neutrophils, a level comparable to S. pneumoniae-challenged, conventionally fed young mice. α-Toc directly inhibited neutrophil egress across epithelial cell monolayers in vitro in response to pneumococci or hepoxilin-A3, an eicosanoid required for pneumococcus-elicited neutrophil trans-epithelial migration. α-Toc altered expression of multiple epithelial and neutrophil adhesion molecules involved in migration, including CD55, CD47, CD18/CD11b, and ICAM-1. These findings suggest that α-Toc enhances resistance of aged mice to bacterial pneumonia by modulating the innate immune response, a finding that has potential clinical significance in combating infection in aged individuals through nutritional intervention.

Indexed as

8,11,14-Eicosatrienoic AcidAge Factorsalpha-TocopherolAnimalsCell Adhesion MoleculesDietary SupplementsDisease Models, AnimalDisease ResistanceDisease SusceptibilityEpitheliumGene ExpressionMaleMiceNeutrophil InfiltrationNeutrophilsPneumonia, Pneumococcal8,11,14-Eicosatrienoic Acid8-hydroxy-11,12-epoxyeicosa-5,9,14-trienoic acidalpha-TocopherolCell Adhesion Molecules

Identifiers

PMID25512603
PMCPMC4834212
OpenAlexW2129715581

What OpenQuestion holds

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LicenceTDM
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.