Evidence map›Paper›PMID 25501908›Full record

ArticleNature medicine2015

In-depth determination and analysis of the human paired heavy- and light-chain antibody repertoire.

Brandon J DeKosky, Takaaki Kojima, Alexa Rodin, Wissam Charab, Gregory C Ippolito, Andrew D Ellington, George Georgiou

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Nature medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 242 papers.

0numbers the graph read from it
0cells of the map it votes in
242citing papers in PubMed
31.1field-weighted citation impact, top 1% 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

242 citing papers in PubMed, 371 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Review
  6. Observational
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. A temporal and spatial atlas of adaptive immune responses in the lymph node following viral infection.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review

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

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

7 authors at 1 institution in 1 country.

Brandon J DeKoskyDepartment of Chemical Engineering, University of Texas at Austin, Austin, Texas, USA.
Takaaki Kojima1] Department of Chemical Engineering, University of Texas at Austin, Austin, Texas, USA. [2] Laboratory of Molecular Biotechnology, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, Japan.
Alexa RodinDepartment of Chemical Engineering, University of Texas at Austin, Austin, Texas, USA.
Wissam CharabDepartment of Chemical Engineering, University of Texas at Austin, Austin, Texas, USA.
Gregory C IppolitoDepartment of Molecular Biosciences, University of Texas at Austin, Austin, Texas, USA.
Andrew D EllingtonCenter for Systems and Synthetic Biology, University of Texas at Austin, Austin, Texas, USA.
George Georgiou1] Department of Chemical Engineering, University of Texas at Austin, Austin, Texas, USA. [2] Department of Molecular Biosciences, University of Texas at Austin, Austin, Texas, USA. [3] Institute for Cellular and Molecular Biology, University of Texas at Austin, Austin, Texas, USA. [4] Department of Biomedical Engineering, University of Texas at Austin, Austin, Texas, USA.
The University of Texas at Austin · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-throughput immune repertoire sequencing has emerged as a critical step in the understanding of adaptive responses following infection or vaccination or in autoimmunity. However, determination of native antibody variable heavy-light pairs (VH-VL pairs) remains a major challenge, and no technologies exist to adequately interrogate the >1 × 10(6) B cells in typical specimens. We developed a low-cost, single-cell, emulsion-based technology for sequencing antibody VH-VL repertoires from >2 × 10(6) B cells per experiment with demonstrated pairing precision >97%. A simple flow-focusing apparatus was used to sequester single B cells into emulsion droplets containing lysis buffer and magnetic beads for mRNA capture; subsequent emulsion RT-PCR generated VH-VL amplicons for next-generation sequencing. Massive VH-VL repertoire analyses of three human donors provided new immunological insights including (i) the identity, frequency and pairing propensity of shared, or 'public', VL genes, (ii) the detection of allelic inclusion (an implicated autoimmune mechanism) in healthy individuals and (iii) the occurrence of antibodies with features, in terms of gene usage and CDR3 length, associated with broadly neutralizing antibodies to rapidly evolving viruses such as HIV-1 and influenza.

Indexed as

Adaptive ImmunityAntibodiesAutoantibodiesB-LymphocytesHigh-Throughput Nucleotide SequencingHIV-1HumansImmunoglobulin Heavy ChainsImmunoglobulin Light ChainsImmunoglobulin Variable RegionRNA, MessengerAntibodiesAutoantibodiesImmunoglobulin Heavy ChainsImmunoglobulin Light ChainsImmunoglobulin Variable RegionRNA, Messenger

Identifiers

PMID25501908
OpenAlexW1979552897

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.