Evidence map›Paper›PMID 37533642›Full record

ArticleCell reports methods2023

TRAPnSeq allows high-throughput profiling of antigen-specific antibody-secreting cells.

Seblewongel Asrat, Joseph C Devlin, Andrea Vecchione, Brian Klotz, Ian Setliff, Devin Srivastava, Andre Limnander, Ashique Rafique, Christina Adler, Stephen Porter and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports methods, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
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  7. Article
  8. Review
  9. Article
  10. Article
  11. Whence and wherefore IgE?Immunological reviews · 2024
    Review
  12. Monoclonal Antibody Generation Using Single B Cell Screening for Treating Infectious Diseases.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2024
    Review
  13. Origins and diversity of pan-isotype human bone marrow plasma cells.bioRxiv : the preprint server for biology · 2024
    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

15 authors at 1 institution in 1 country.

Seblewongel AsratRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Joseph C DevlinRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Andrea VecchioneRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Brian KlotzRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Ian SetliffRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Devin SrivastavaRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Andre LimnanderRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Ashique RafiqueRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Christina AdlerRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Stephen PorterRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Andrew J MurphyRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Gurinder S AtwalRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Matthew A SleemanRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Wei Keat LimRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Jamie M OrengoRegeneron Pharmaceuticals, Tarrytown, NY 10591, USA.
Regeneron (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Following activation by cognate antigen, B cells undergo fine-tuning of their antigen receptors and may ultimately differentiate into antibody-secreting cells (ASCs). While antigen-specific B cells that express surface receptors (B cell receptors [BCRs]) can be readily cloned and sequenced following flow sorting, antigen-specific ASCs that lack surface BCRs cannot be easily profiled. Here, we report an approach, TRAPnSeq (antigen specificity mapping through immunoglobulin [Ig] secretion TRAP and Sequencing), that allows capture of secreted antibodies on the surface of ASCs, which in turn enables high-throughput screening of single ASCs against large antigen panels. This approach incorporates flow cytometry, standard microfluidic platforms, and DNA-barcoding technologies to characterize antigen-specific ASCs through single-cell V(D)J, RNA, and antigen barcode sequencing. We show the utility of TRAPnSeq by profiling antigen-specific IgG and IgE ASCs from both mice and humans and highlight its capacity to accelerate therapeutic antibody discovery from ASCs.

Indexed as

Antibody-Producing CellsAntigensAnimalsAntibodiesB-LymphocytesHumansMiceReceptors, Antigen, B-CellAntibodiesAntigensReceptors, Antigen, B-Cellantibody-secreting cellsIgEIgGplasmablastsplasma cellsrepertoire analysissecretion trap

Identifiers

PMID37533642
PMCPMC10391570
OpenAlexW4383558895

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.