Evidence map›Paper›PMID 23980154›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Converting stem cells to dendritic cells by agonist antibodies from unbiased morphogenic selections.

Kyungmoo Yea, Hongkai Zhang, Jia Xie, Teresa M Jones, Guang Yang, Byeong Doo Song, Richard A Lerner

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.6field-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

15 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Selection of a Full Agonist Combinatorial Antibody that Rescues Leptin Deficiency In Vivo.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    Article
  4. Article
  5. Article
  6. Article
  7. Interferon-γ is a master checkpoint regulator of cytokine-induced differentiation.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  8. Review
  9. An agonist antibody that blocks autoimmunity by inducing anti-inflammatory macrophages.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    Article
  10. Activating pleiotropic receptors to kill cancer cells.Cell cycle (Georgetown, Tex.) · 2016
    Article
  11. Agonist antibody that induces human malignant cells to kill one another.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  12. Review
  13. Review
  14. Article
  15. Directing stem cell differentiation with antibodies.Proceedings of the National Academy of Sciences of the United States of America · 2013
    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

7 authors at 3 institutions in 3 countries.

Kyungmoo YeaThe Scripps Korea Antibody Institute, Chuncheon-si 200-701, South Korea.
Hongkai Zhang
Jia Xie
Teresa M Jones
Guang Yang
Byeong Doo Song
Richard A Lerner
Scripps Research Institute · USScripps Korea Antibody Institute · KRShanghaiTech University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

When combinatorial antibody libraries are rendered infectious for eukaryotic cells, the integrated antibody genotype and cellular phenotype become permanently linked and each cell becomes a selection system unto itself. These systems should be ideal for the identification of proteins and pathways that regulate differentiation so long as selection systems can be devised. Here we use a selection system based on the ability of secreted antibodies to alter the morphology of colonies expressing them when grown in soft agar. Importantly, this approach is different from all previous studies in that it used a pure discovery format where unbiased libraries that were not preselected against any known protein were used as probes. As such, the strategy is analogous to classical forward genetic approaches except that it operates directly at the protein level. This approach led to the identification of integrin-binding agonist antibodies that efficiently converted human stem cells to dendritic cells.

Indexed as

AntibodiesAmino Acid SequenceCell DifferentiationCell LineCell LineageComplementarity Determining RegionsDendritic CellsEvolution, MolecularHematopoietic Stem CellsHumansIntegrinsMolecular Sequence DataOligopeptidesPeptide LibraryAntibodiesarginyl-glycyl-aspartic acidComplementarity Determining RegionsIntegrinsOligopeptidesPeptide Libraryintracellular combinatorial antibodiesphenotypic selections

Identifiers

PMID23980154
PMCPMC3773771
OpenAlexW2037411233

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.