Evidence map›Paper›PMID 31348721›Full record

ArticlemAbs2019

Characterization of a single reporter-gene potency assay for T-cell-dependent bispecific molecules.

Ho Young Lee, Ames Register, Jeongsup Shim, Edward Contreras, Qiang Wu, Guoying Jiang

Open access · goldAbstract read
In one paragraph

Article in mAbs, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Bioassay Development for Bispecific Antibodies-Challenges and Opportunities.International journal of molecular sciences · 2021
    Review
  6. Article
  7. 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

6 authors at 1 institution in 1 country.

Ho Young LeeBiological Technologies, Department of Analytical Development and Quality Control, Genentech, A member of the Roche group , South San Francisco , CA , USA.
Ames RegisterBiological Technologies, Department of Analytical Development and Quality Control, Genentech, A member of the Roche group , South San Francisco , CA , USA.ORCID 0000-0002-6167-9980
Jeongsup ShimBiological Technologies, Department of Analytical Development and Quality Control, Genentech, A member of the Roche group , South San Francisco , CA , USA.ORCID 0000-0001-8390-9671
Edward ContrerasBiological Technologies, Department of Analytical Development and Quality Control, Genentech, A member of the Roche group , South San Francisco , CA , USA.
Qiang WuBiological Technologies, Department of Analytical Development and Quality Control, Genentech, A member of the Roche group , South San Francisco , CA , USA.ORCID 0000-0001-6892-8815
Guoying JiangBiological Technologies, Department of Analytical Development and Quality Control, Genentech, A member of the Roche group , South San Francisco , CA , USA.ORCID 0000-0002-8059-0893
La Roche College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell-dependent bispecific antibodies (TDBs) are promising cancer immunotherapies that recruit patients' T cells to kill cancer cells. There are many TDBs in clinical trials, demonstrating their widely recognized therapeutic potential. However, their complex, multi-step mechanism of action (MoA), which includes bispecific antigen binding, T-cell activation, and target-cell killing, presents unique challenges for biological characterization and potency assay selection. Here, we describe the development of a

Indexed as

Immunologic TechniquesAntibodies, BispecificAntigensCytotoxicity, ImmunologicGenes, ReporterHumansImmunotherapyJurkat CellsLuciferasesLymphocyte ActivationNeoplasmsT-LymphocytesAntibodies, BispecificAntigensLuciferasesbiological characterization strategybispecific antibodies (BsAbs)mechanism of action (MoA)reporter gene potency assayT cell activationT-cell-dependent bispecific antibodies (TDBs)

Identifiers

PMID31348721
PMCPMC6748617
OpenAlexW2964876228

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.