Evidence map›Paper›PMID 27658954›Full record

ArticleScientific reports2016

Decreased IL7Rα and TdT expression underlie the skewed immunoglobulin repertoire of human B-cell precursors from fetal origin.

Magdalena B Rother, Kristin Jensen, Mirjam van der Burg, Fleur S van de Bovenkamp, Roel Kroek, Wilfred F J van IJcken, Vincent H J van der Velden, Tom Cupedo, Ole K Olstad, Jacques J M van Dongen and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. B1 Cells for Life.Immunological reviews · 2026
    Review
  2. Article
  3. Do human B-1 lymphocytes truly exist?Frontiers in immunology · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. mTORC1 as a cell-intrinsic rheostat that shapes development, preimmune repertoire, and function of B lymphocytes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  11. Article
  12. Article
  13. Cell circuits between B cell progenitors and IL-7The Journal of experimental medicine · 2018
    Article
  14. Article
  15. Article
  16. Review
  17. 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

11 authors at 2 institutions in 3 countries.

Magdalena B RotherDepartment of Immunology, Erasmus MC, University Medical Center Rotterdam, The Netherlands.
Kristin JensenDepartment of Medical Biochemistry, Oslo University Hospital, Norway.
Mirjam van der BurgDepartment of Immunology, Erasmus MC, University Medical Center Rotterdam, The Netherlands.
Fleur S van de BovenkampDepartment of Immunology, Erasmus MC, University Medical Center Rotterdam, The Netherlands.
Roel KroekDepartment of Immunology, Erasmus MC, University Medical Center Rotterdam, The Netherlands.
Wilfred F J van IJckenCenter for Biomics, Erasmus MC, University Medical Center Rotterdam, The Netherlands.
Vincent H J van der VeldenDepartment of Immunology, Erasmus MC, University Medical Center Rotterdam, The Netherlands.
Tom CupedoDepartment of Hematology, Erasmus MC, University Medical Center Rotterdam, The Netherlands.
Ole K OlstadDepartment of Medical Biochemistry, Oslo University Hospital, Norway.
Jacques J M van DongenDepartment of Immunology, Erasmus MC, University Medical Center Rotterdam, The Netherlands.
Menno C van ZelmDepartment of Immunology, Erasmus MC, University Medical Center Rotterdam, The Netherlands.
Erasmus MC · NLOslo University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Newborns are unable to mount antibody responses towards certain antigens. This has been related to the restricted repertoire of immunoglobulin (Ig) genes of their B cells. The mechanisms underlying the restricted fetal Ig gene repertoire are currently unresolved. We here addressed this with detailed molecular and cellular analysis of human precursor-B cells from fetal liver, fetal bone marrow (BM), and pediatric BM. In the absence of selection processes, fetal B-cell progenitors more frequently used proximal V, D and J genes in complete IGH gene rearrangements, despite normal Ig locus contraction. Fewer N-nucleotides were added in IGH gene rearrangements in the context of low TdT and XRCC4 expression. Moreover, fetal progenitor-B cells expressed lower levels of IL7Rα than their pediatric counterparts. Analysis of progenitor-B cells from IL7Rα-deficient patients revealed that TdT expression and N-nucleotides additions in Dh-Jh junctions were dependent on functional IL7Rα. Thus, IL7Rα affects TdT expression, and decreased expression of this receptor underlies at least in part the skewed Ig repertoire formation in fetal B-cell precursors. These new insights provide a better understanding of the formation of adaptive immunity in the developing fetus.

Identifiers

PMID27658954
PMCPMC5034271
OpenAlexW2523450927

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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.