Evidence map›Paper›PMID 36524207›Full record

ArticleOncoimmunology2022

Generation and functional characterization of a multigene-modified NK101 cell line exerting diverse mechanisms of antitumor action.

Injung Hwang, Hyun Tak Jin, Moon Cheol Kang, Tae Yoon Kim, Young Chul Sung, Sae Won Kim

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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 3 institutions in 3 countries.

Injung HwangSL BiGen, Inc., Research Institute, Incheon, Republic of Korea.
Hyun Tak JinProgen. Co., Ltd., Research Institute, Seongnam, Republic of Korea.
Moon Cheol KangSL BiGen, Inc., Research Institute, Incheon, Republic of Korea.
Tae Yoon KimSL BiGen, Inc., Research Institute, Incheon, Republic of Korea.
Young Chul SungDivision of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Sae Won KimSL BiGen, Inc., Research Institute, Incheon, Republic of Korea.
Sugen Life Sciences (India) · INLigand Pharmaceuticals (United Kingdom) · GBPohang University of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clonal cell line-based, multigene-modified, off-the-shelf NK cell therapeutics are emerging as the new frontier of adoptive cellular immunotherapy. Here, we utilized a newly established NK cell line, NK101, as a backbone to derive multifaceted killer cells armored with various antitumor modalities through repeated cycles of genetic modification and clonal selection. First, NK101 cells were transduced with a tricistronic lentiviral vector expressing CD7, CD28, and cytosine deaminase (CD). The resulting cell line demonstrated enhanced cytotoxicity against B7

Indexed as

Cytotoxicity, ImmunologicKiller Cells, NaturalCell Line, TumorImmunotherapy, AdoptiveTransforming Growth Factor betaTransforming Growth Factor betaadoptive cellular immunotherapymultiple genetic engineeringNK101 cell line

Identifiers

PMID36524207
PMCPMC9746629
OpenAlexW4206442654

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.