Evidence map›Paper›PMID 28000661›Full record

Observational studyNature communications2016

Temporal stability and molecular persistence of the bone marrow plasma cell antibody repertoire.

Gabriel C Wu, Nai-Kong V Cheung, George Georgiou, Edward M Marcotte, Gregory C Ippolito

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Structural promiscuity in the human circulatory IgA1 clonal repertoire.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Long-term B cell memory emerges at uniform relative rates in the human immune response.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Long-Lived Plasma Cells in Mice and Men.Frontiers in immunology · 2018
    Review
  8. Article
  9. 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 2 institutions in 1 country.

Gabriel C WuCenter for Systems and Synthetic Biology, University of Texas at Austin, Austin, Texas 78712, USA.
Nai-Kong V CheungDepartment of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, New York 10065, USA.
George GeorgiouDepartment of Molecular Biosciences, University of Texas at Austin, Austin, Texas 78712, USA.
Edward M MarcotteCenter for Systems and Synthetic Biology, University of Texas at Austin, Austin, Texas 78712, USA.
Gregory C IppolitoDepartment of Molecular Biosciences, University of Texas at Austin, Austin, Texas 78712, USA.
The University of Texas at Austin · USMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Plasma cells in human bone marrow (BM) are thought to be responsible for sustaining lifelong immunity, but its underlying basis is controversial. Here we use high-throughput sequence analysis of the same individual across 6.5 years to show that the BM plasma cell immunoglobulin heavy chain repertoire is remarkably stable over time. We find a nearly static bias in individual and combinatorial gene usage across time. Analysis of a second donor corroborates these observations. We also report the persistence of numerous BM plasma cell clonotypes (∼2%) identifiable at all points assayed across 6.5 years, supporting a model of serological memory based upon intrinsic longevity of human plasma cells. Donors were adolescents who completely recovered from neuroblastoma prior to the start of this study. Our work will facilitate differentiation between healthy and diseased antibody repertoires, by serving as a point of comparison with future deep-sequencing studies involving immune intervention.

Indexed as

AdolescentAmino Acid SequenceAntibodiesAntibody FormationBone MarrowBone Marrow CellsChildFemaleHigh-Throughput Nucleotide SequencingHumansImmunoglobulin Heavy ChainsMaleNeuroblastomaPlasma CellsProspective StudiesAntibodiesImmunoglobulin Heavy Chains

Identifiers

PMID28000661
PMCPMC5187582
OpenAlexW2952202842

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.