Evidence map›Paper›PMID 18519648›Full record

ArticleThe Journal of experimental medicine2008

Somatic diversification in the absence of antigen-driven responses is the hallmark of the IgM+ IgD+ CD27+ B cell repertoire in infants.

Sandra Weller, Maria Mamani-Matsuda, Capucine Picard, Corinne Cordier, Damiana Lecoeuche, Frédéric Gauthier, Jean-Claude Weill, Claude-Agnès Reynaud

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

89 citing papers in PubMed, 156 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. NF-kB's contribution to B cell fate decisions.Frontiers in immunology · 2023
    Review
  5. Asplenia and spleen hypofunction.Nature reviews. Disease primers · 2022
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Homeostasis and regulation of autoreactive B cells.Cellular & molecular immunology · 2020
    Review
  11. Prenatal development of human immunity.Science (New York, N.Y.) · 2020
    Review
  12. Article
  13. Innate B Cells: the Archetype of Protective Immune Cells.Clinical reviews in allergy & immunology · 2020
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Article

29 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Sandra WellerInstitut National de la Santé et de la Recherche Médicale U783, Développement du Système Immunitaire, Université Paris Descartes, Faculté de Médecine, Site Necker Enfants-Malades, Paris 75015, France.
Maria Mamani-Matsuda
Capucine Picard
Corinne Cordier
Damiana Lecoeuche
Frédéric Gauthier
Jean-Claude Weill
Claude-Agnès Reynaud
Inserm · FRBicêtre Hospital · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cell-dependent immune responses develop soon after birth, whereas it takes 2 yr for humans to develop T cell-independent responses. We used this dissociation to analyze the repertoire diversification of IgM(+)IgD(+)CD27(+) B cells (also known as "IgM memory" B cells), comparing these cells with switched B cells in children <2 yr of age, with the aim of determining whether these two subsets are developmentally related. We show that the repertoire of IgM(+)IgD(+)CD27(+) B cells in the spleen and blood displays no sign of antigen-driven activation and expansion on H-CDR3 spectratyping, despite the many antigenic challenges provided by childhood vaccinations. This repertoire differed markedly from those of switched B cells and splenic germinal center B cells, even at the early stage of differentiation associated with mu heavy chain expression. These data provide evidence for the developmental diversification of IgM(+)IgD(+)CD27(+) B cells, at least in very young children, outside of T cell-dependent and -independent immune responses.

Indexed as

Genetic VariationAntigens, CDB-LymphocytesB-Lymphocyte SubsetsGene RearrangementHumansImmunoglobulin DImmunoglobulin MImmunoglobulin mu-ChainsImmunoglobulin Variable RegionImmunologic MemoryInfantLymphocyte ActivationSpleenT-LymphocytesTranscription, GeneticAntigens, CDImmunoglobulin DImmunoglobulin MImmunoglobulin mu-ChainsImmunoglobulin Variable RegionTumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID18519648
PMCPMC2413031
OpenAlexW2101727960

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.