Evidence map›Paper›PMID 34886888›Full record

ArticleJournal of hematology & oncology2021

Bispecific antibody-activated T cells enhance NK cell-mediated antibody-dependent cellular cytotoxicity.

Zhaoming Wang, Chaobo Yin, Lawrence G Lum, Andrean Simons, George J Weiner

Open access · goldAbstract readLetter
In one paragraph

Article in Journal of hematology & oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. 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.

Zhaoming WangHolden Comprehensive Cancer Center, University of Iowa, 5970-Z JPP, 200 Hawkins Drive, Iowa City, IA, 52242, USA.
Chaobo YinHolden Comprehensive Cancer Center, University of Iowa, 5970-Z JPP, 200 Hawkins Drive, Iowa City, IA, 52242, USA.
Lawrence G LumDivision of Hematology/Oncology, Department of Medicine, The University of Virginia, Charlottesville, VA, USA.
Andrean SimonsHolden Comprehensive Cancer Center, University of Iowa, 5970-Z JPP, 200 Hawkins Drive, Iowa City, IA, 52242, USA.
George J WeinerHolden Comprehensive Cancer Center, University of Iowa, 5970-Z JPP, 200 Hawkins Drive, Iowa City, IA, 52242, USA. george-weiner@uiowa.edu.ORCID 0000-0003-3427-0562
University of Iowa · USUniversity of Virginia · US

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Thomas P. Loughran · 1987 to 2026
$72.1M
Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Douglas Robert Spitz · 2000 to 2026
$70.0M
The Role of Monocytes in non-Hodgkin LymphomaP50CA097274 · NCI · UNIVERSITY OF IOWA · PI WEINER, GEORGE J. · 2002 to 2021
$45.7M
Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Brandi Janssen · 1990 to 2026
$40.5M
Targeting Neuroblastoma with armed T cellsR01CA182526 · NCI · WAYNE STATE UNIVERSITY · PI CHEUNG, NAI-KONG V, LUM, LAWRENCE G · 2014 to 2019
$3.9M
NCI NIH HHS P30 CA044579NCI NIH HHS P30 CA86862NCI NIH HHS P50 CA97274NCI NIH HHS R01 CA182526NIEHS NIH HHS P30 ES005605
6 · The paper itself

Abstract

Resistance to anti-cancer monoclonal antibody (mAb) therapy remains a clinical challenge. Previous work in our laboratory has shown that T cell help in the form of interleukin-2 maintains long-term NK cell viability and NK cell-mediated antibody-dependent cellular cytotoxicity (ADCC). Lack of such T cell help may be a potential mechanism for resistance to mAb therapy. Here, we evaluate whether concomitant treatment with anti-CD3 × anti-cancer bispecific antibodies (bsAbs) can overcome this resistance by enhancing T cell help, and thereby maintaining long-term NK cell-mediated ADCC. Normal donor peripheral blood mononuclear cells were depleted of T cells, replenished with defined numbers of autologous T cells (from 0.75 to 50%) and co-cultured with mono-/bispecific antibody-treated target tumor cells for up to 7 days. At low T cell concentrations, bsAb-activated T cells (mainly CD4

Indexed as

Antibodies, BispecificAntibody-Dependent Cell CytotoxicityAntineoplastic Agents, ImmunologicalCells, CulturedHumansKiller Cells, NaturalLymphocyte ActivationT-LymphocytesAntibodies, BispecificAntineoplastic Agents, ImmunologicalblinatumomabADCCAnti-CD20Bispecific antibodyBlinatumomabNK cell

Identifiers

PMID34886888
PMCPMC8656063
OpenAlexW4200502215

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.