Evidence map›Paper›PMID 29443377›Full record

ArticleHepatology (Baltimore, Md.)2018

Identification of α-fetoprotein-specific T-cell receptors for hepatocellular carcinoma immunotherapy.

Wei Zhu, Yibing Peng, Lan Wang, Yuan Hong, Xiaotao Jiang, Qi Li, Heping Liu, Lei Huang, Juan Wu, Esteban Celis and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 3% 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

78 citing papers in PubMed, 1 synthesis or guideline pooled it, 100 citations in OpenAlex.

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18 more citing papers are in PubMed but not listed here.

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

13 authors at 3 institutions in 3 countries.

Wei ZhuGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA.
Yibing PengGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA.
Lan WangGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA.
Yuan HongGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA.
Xiaotao JiangGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA.
Qi LiGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA.
Heping LiuGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA.
Lei HuangGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA.
Juan WuGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA.
Esteban CelisGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA.
Todd MerchenGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA.
Edward KruseGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA.
Yukai HeGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA.
Augusta University · USNewcastle University · GBPeking University First Hospital · CN

Funding

TCR engineering of human T cells for immunotherapy of hepatocellular carcinomaR01CA235159 · NCI · AUGUSTA UNIVERSITY · PI HE, YUKAI · 2019 to 2024
$1.9M
Engineering alpha fetoprotein and glypican-3 to develop hepatoma (HCC) vaccinesR01CA168912 · NCI · AUGUSTA UNIVERSITY · PI HE, YUKAI · 2014 to 2018
$1.6M
NCI NIH HHS R01 CA168912NCI NIH HHS R01 CA235159
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the major form of liver cancer for which there is no effective therapy. Genetic modification with T-cell receptors (TCRs) specific for HCC-associated antigens, such as α-fetoprotein (AFP), can potentially redirect human T cells to specifically recognize and kill HCC tumor cells to achieve antitumor effects. In this study, using lentivector and peptide immunization, we identified a population of cluster of differentiation 8 (CD8) T cells in human leukocyte antigen (HLA)-A2 transgenic AAD mice that recognized AFP

conclusionWe have identified AFP-specific murine TCR genes that can redirect human T cells to specifically recognize and kill HCC tumor cells, and those AFP

Indexed as

alpha-FetoproteinsAnimalsCarcinoma, HepatocellularCD8-Positive T-LymphocytesCell Line, TumorEnzyme-Linked Immunosorbent AssayFemaleHep G2 CellsHLA-A2 AntigenHumansImmunotherapyLiver NeoplasmsMiceMice, TransgenicReceptors, Antigen, T-Cellalpha-FetoproteinsHLA-A2 AntigenReceptors, Antigen, T-Cell

Identifiers

PMID29443377
PMCPMC7368991
OpenAlexW2793199674

What OpenQuestion holds

Textmetadata
LicenceTDM
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.