Evidence map›Paper›PMID 27712994›Full record

ArticleExperimental and molecular pathology2016

Identification of high-affinity anti-CD16A allotype-independent human antibody domains.

Wei Li, Hongjia Yang, Dimiter S Dimitrov

Open access · greenAbstract read
In one paragraph

Article in Experimental and molecular pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. AntiBMPNN: Structure-Guided Graph Neural Networks for Precision Antibody Engineering.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Recombinant Antibodies to Arm Cytotoxic Lymphocytes in Cancer Immunotherapy.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2017
    Review
  10. Article
  11. Precision immunomedicine.Emerging microbes & infections · 2017
    Article
  12. 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

3 authors at 2 institutions in 1 country.

Wei LiProtein Interactions Section, Cancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA. Electronic address: wei.li3@nih.gov.
Hongjia YangPalisades Charter High School, 15777 Bowdoin St, Pacific Palisades, CA 90272, USA.
Dimiter S DimitrovProtein Interactions Section, Cancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA. Electronic address: dimitrdi@mail.nih.gov.
Center for Cancer Research · USNational Institutes of Health · US

Funding

Human Monoclonal Antibodies Against CancerZIABC010701 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DIMITROV, DIMITER S · 2009 to 2017
$6.9M
Human Monoclonal Antibodies and Antibody-Guided NanoparticlesZ01BC010701 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DIMITROV, DIMITER S · 2006 to 2008
$2.6M
Viral Envelope Glycoprotein Interactions with ReceptorsZ01BC010257 · BC · BASIC SCIENCES · PI DIMITROV, DIMTER S. · 1996 to 2005
–
Intramural NIH HHS Z01 BC010257Intramural NIH HHS Z01 BC010701
6 · The paper itself

Abstract

CD16A (FcγRIIIA) is an activating receptor mostly expressed on natural killer (NK) cells and monocytes/macrophages. It can mediate antibody-dependent cell-mediated cytotoxicity (ADCC) through low-affinity interaction with human immunoglobulin G (IgG) Fc. It can also mediate cell lysis if NK cells are guided by bispecific killer cells engagers (BiKEs). BiKEs showed some success in clinical trials of cancer and are promising candidate therapeutics. However, currently reported BiKEs are based on antibody fragments (scFvs) of relatively large size. The CD16A-specific antibodies are also typically from animal origin. Decreasing the BiKE size could result in enhanced penetration into solid tumor and normal tissues, and using fully human antibodies could decrease the likelihood of immunogenicity. Here we report the identification and characterization of two antibody domains, D6 and E11, isolated from a very large human VH antibody domain library displayed on phage. D6 and E11 bound CD16A with EC

Indexed as

Antibody AffinityAntibody SpecificityCell MembraneElectrophoresis, Polyacrylamide GelEnzyme-Linked Immunosorbent AssayEpitopesFlow CytometryHumansImmunoglobulin AllotypesInterleukin-2Jurkat CellsKiller Cells, NaturalLymphocyte ActivationMolecular Docking SimulationProtein BindingProtein DomainsEpitopesFCGR3A protein, humanImmunoglobulin AllotypesInterleukin-2Receptors, IgGRecombinant ProteinsADCCAntibody domainsBiKECD16ANatural killer (NK) cells

Identifiers

PMID27712994
PMCPMC6957250
OpenAlexW2529333096

What OpenQuestion holds

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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.