Evidence map›Paper›PMID 35012922›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2021

[Construction and evaluation of dual-effect cord blood natural killer cells expressing highaffinity PD-1 and chimeric antigen CD19 receptor].

H Zhong, Q Zou, H Liu, X Wang, S DU, H Liang, Z Wu, J Ye, Q Zou

Open access · greenAbstract read
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 82% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Review
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

9 authors at 2 institutions in 1 country.

H ZhongGuangzhou Cedicine Biotech Co.Ltd, Guangzhou 510633, China.
Q ZouSchool of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, China.
H LiuGuangzhou Cedicine Biotech Co.Ltd, Guangzhou 510633, China.
X WangSchool of Life Sciences, Westlake University, Hangzhou 310024, China.
S DUGuangzhou Cedicine Biotech Co.Ltd, Guangzhou 510633, China.
H LiangGuangzhou Cedicine Biotech Co.Ltd, Guangzhou 510633, China.
Z WuGuangzhou Cedicine Biotech Co.Ltd, Guangzhou 510633, China.
J YeGuangzhou Cedicine Biotech Co.Ltd, Guangzhou 510633, China.
Q ZouGuangzhou Cedicine Biotech Co.Ltd, Guangzhou 510633, China.
Westlake University · CNWuyi University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo obtain novel dual-effect cord blood natural killer cells (CBNKCs) expressing high-affinity PD-1 (HAPD1) and chimeric antigen CD19 receptor (CAR) to improve the effect of CAR-based immunotherapy.

methodsA dual-effect lentiviral vector expressing both HAPD1 and CAR targeting CD19 was constructed. CBNKCs were infected with the vector to obtain HAPD1 CAR19 CBNKCs. The surface markers of the cells including CD3

resultsCBNKCs were successfully transduced with T-cell designed CAR19 and HAPD1 CAR19 with an efficiency of (18.63±1.88)%. Infection with the lentiviral vector significantly reduced the cell expansion efficiency of the CBNKCs (10.97±2.77

conclusionWe obtained a novel dual-effect CBNKC co-expressing HAPD1 and CAR. The cells show strong cytotoxicity against the target tumor cells both

Indexed as

Receptors, Chimeric AntigenAnimalsAntigens, CD19Cell Line, TumorFetal BloodImmunotherapy, AdoptiveKiller Cells, NaturalMiceProgrammed Cell Death 1 ReceptorAntigens, CD19Programmed Cell Death 1 ReceptorReceptors, Chimeric Antigenantitumor efficacychimeric antigen receptorcord blood NK cellshigh-affinity PD-1immunophenotypes

Identifiers

PMID35012922
PMCPMC8752428
OpenAlexW4206770945

What OpenQuestion holds

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Registered trials

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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.