Evidence map›Paper›PMID 35883606›Full record

ArticleCells2022

Therapeutic Potential of Ex Vivo Expanded γδ T Cells against Osteosarcoma Cells.

Yunmi Ko, Yeon Ho Jeong, Jun Ah Lee

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. 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
0.4field-weighted citation impact, top 37% 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, 4 citations in OpenAlex.

  1. 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.

Yunmi KoCenter for Pediatric Cancer, Department of Pediatrics, National Cancer Center, Goyang 10408, Korea.ORCID 0000-0002-0562-2787
Yeon Ho JeongDepartment of Medical Biotechnology, College of Biomedical Science, Kangwon National University, Chuncheon 24341, Korea.
Jun Ah LeeCenter for Pediatric Cancer, Department of Pediatrics, National Cancer Center, Goyang 10408, Korea.ORCID 0000-0003-3310-9566
Kangwon National University · KRNational Cancer Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy is an attractive therapeutic strategy for the treatment of osteosarcoma (OS). The unique features of γδ T cells have made them popular for cancer immunotherapy. Here, we expanded γδ T cells using human peripheral blood mononuclear cells (PBMCs) and investigated their therapeutic potential against OS cells. PBMCs from healthy donors were cultured for 10 days with CON medium (unstimulated control); EX media, CON with recombinant human interleukin-2 (rhIL-2) and zoledronate; and EX28 media, CON with rhIL-2, zoledronate, and CD3/CD28 activator. The expanded γδ T cells were isolated by magnetic cell separation or fluorescence-activated cell sorting, cultured with two OS cell lines (KHOS/NP and MG-63) at various cell ratios with or without doxorubicin or ifosfamide, and analyzed for cytotoxicity and cytokine secretion. The number of CD3

Indexed as

Bone NeoplasmsOsteosarcomaReceptors, Antigen, T-Cell, gamma-deltaCD28 AntigensDiphosphonatesHumansImidazolesLeukocytes, MononuclearT-LymphocytesZoledronic AcidCD28 AntigensDiphosphonatesImidazolesReceptors, Antigen, T-Cell, gamma-deltaZoledronic Acidchemo-immunotherapychemotherapeutic agentsimmunotherapymononuclear cellsosteosarcomaperipheral bloodγδ T cells

Identifiers

PMID35883606
PMCPMC9318146
OpenAlexW4285044003

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.