Evidence map›Paper›PMID 16239548›Full record

Trial reportInfection and immunity2005

Immune response to pneumococcal polysaccharides 4 and 14 in elderly and young adults: analysis of the variable heavy chain repertoire.

Kris Kolibab, S Louise Smithson, Bradley Rabquer, Sadik Khuder, M A Julie Westerink

Open access · greenAbstract readClinical TrialComparative Study
In one paragraph

Trial report in Infection and immunity, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

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  20. Phenotypic analysis of pneumococcal polysaccharide-specific B cells.Journal of immunology (Baltimore, Md. : 1950) · 2012
    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

5 authors at 1 institution in 1 country.

Kris KolibabDepartment of Medicine, Medical University of Ohio at Toledo, Health Education Building, 3000 Arlington Ave., Toledo, OH 43614, USA.
S Louise Smithson
Bradley Rabquer
Sadik Khuder
M A Julie Westerink
University of Toledo Medical Center · US

Funding

Elderly Immune Response to Pneumococcal PolysaccharideR01AG015978 · NIA · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI WESTERINK, M.A. JULIA · 2000 to 2010
$2.4M
NIA NIH HHS AG15978NIA NIH HHS R01 AG015978
6 · The paper itself

Abstract

Streptococcus pneumoniae is a leading cause of morbidity and mortality in both developed and developing countries. The current pneumococcal polysaccharide (PPS) vaccine is highly effective in young adults; however, vaccine efficacy is dramatically decreased in the elderly population. We hypothesized that the decreased vaccine efficacy in the elderly results from altered variable gene family usage. We have characterized the immunoglobulin G gene usage of the antibody response to PPS4 and PPS14 in 20 young and 20 elderly adults. The variable heavy (V(H)) gene repertoire of human peripheral B cells was amplified by using PCR. A total of 364 heavy chain sequences with specificity for PPS4 and 305 heavy chain sequences for PPS14 were analyzed from young adults. In addition, a total of 325 sequences for PPS4 and 291 sequences for PPS14 were obtained from elderly adults. Complete sequence identity, somatic mutation frequencies, and V(H) gene usage was determined in response to PPS4 and PPS14. In all volunteers, the immune response to both polysaccharides consisted predominantly of heavy chains belonging to the V(H)3 gene family. There were significant differences in the variable gene repertoire between young and elderly adults. Somatic mutation occurred more frequently in sequences derived from young compared to elderly derived sequences. With aging, a loss of oligoclonality was noted in response to PPS4 and PPS14 compared to young adults. The observed differences in V(H) repertoire, somatic mutation, and loss of oligoclonality may contribute to decreased vaccine efficacy in the elderly.

Indexed as

AdultAgedAgingAmino Acid SequenceAntibodies, BacterialAntibody AffinityBacterial CapsulesB-LymphocytesGene Expression RegulationGerm CellsHumansImmunoglobulin Heavy ChainsMolecular Sequence DataMutationPneumococcal VaccinesPolysaccharides, BacterialAntibodies, BacterialImmunoglobulin Heavy Chainspneumococcal polysaccharide, type 14Pneumococcal Vaccinespneumonococcal polysaccharide, type 4Polysaccharides, Bacterial

Identifiers

PMID16239548
PMCPMC1273876
OpenAlexW2146439877

What OpenQuestion holds

Textmetadata
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.