Evidence map›Paper›PMID 36275712›Full record

ArticleFrontiers in immunology2022

Reducing farnesyl diphosphate synthase levels activates Vγ9Vδ2 T cells and improves tumor suppression in murine xenograft cancer models.

Mei-Ling Liou, Tyler Lahusen, Haishan Li, Lingzhi Xiao, C David Pauza

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 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
0.3field-weighted citation impact, top 49% 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, 3 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

5 authors.

Mei-Ling LiouAmerican Gene Technologies International Inc., Rockville, MD, United States.
Tyler LahusenAmerican Gene Technologies International Inc., Rockville, MD, United States.
Haishan LiAmerican Gene Technologies International Inc., Rockville, MD, United States.
Lingzhi XiaoAmerican Gene Technologies International Inc., Rockville, MD, United States.
C David PauzaAmerican Gene Technologies International Inc., Rockville, MD, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human Vγ9Vδ2 T cells are attractive candidates for cancer immunotherapy due to their potent capacity for tumor recognition and cytolysis of many tumor cell types. However, efforts to deploy clinical strategies for Vγ9Vδ2 T cell cancer therapy are hampered by insufficient potency. We are pursuing an alternate strategy of modifying tumors to increase the capacity for Vγ9Vδ2 T cell activation, as a means for strengthening the anti-tumor response by resident or ex vivo manufactured Vγ9Vδ2 T cells. Vγ9Vδ2 T cells are activated

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAnimalsGeranyltranstransferaseHeterograftsHumansInterleukin-2MaleMiceReceptors, Antigen, T-Cell, gamma-deltaRNARNA, MessengerT-LymphocytesGeranyltranstransferaseInterleukin-2Receptors, Antigen, T-Cell, gamma-deltaRNARNA, MessengercancerFDPSgamma delta T-cellimmunotherapyshRNAT-celltumor

Identifiers

PMID36275712
PMCPMC9581136
OpenAlexW4301430774

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.