Evidence map›Paper›PMID 26332693›Full record

ReviewClinical and experimental immunology2016

The ageing human B cell repertoire: a failure of selection?

D K Dunn-Walters

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical and experimental immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

38 citing papers in PubMed, 68 citations in OpenAlex.

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  18. Sex-Biased Aging Effects on Ig Somatic Hypermutation Targeting.Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
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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

1 author at 1 institution in 1 country.

D K Dunn-WaltersFaculty of Life Sciences & Medicine, King's College London, London, UK.
King's College London · GB

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council MR/L01257X/1Medical Research Council MR/L01257X/2The Dunhill Medical Trust R279/0213
6 · The paper itself

Abstract

B cells undergo a number of different developmental stages, from initial formation of their B cell receptor (BCR) genes to differentiation into antibody-secreting plasma cells. Because the BCR is vital in these differentiation steps, autoreactive and exogenous antigen binding to the BCR exert critical selection pressures to shape the B cell repertoire. Older people are more prone to infectious disease, less able to respond well to vaccination and more likely to have autoreactive antibodies. Here we review evidence of changes in B cell repertoires in older people, which may be a reflection of age-related changes in B cell selection processes.

Indexed as

Clonal Selection, Antigen-MediatedImmunity, HumoralAgingAnimalsAntibody DiversityAutoantibodiesB-LymphocytesCell DifferentiationHumansReceptors, Antigen, B-CellAutoantibodiesReceptors, Antigen, B-CellageingantibodiesB cellrepertoireselection

Identifiers

PMID26332693
PMCPMC4687518
OpenAlexW1923950548

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.