Evidence map›Paper›PMID 17457217›Full record

ArticleJournal of immunotherapy (Hagerstown, Md. : 1997)

AFP-specific CD4+ helper T-cell responses in healthy donors and HCC patients.

Viktoria N Evdokimova, Yang Liu, Douglas M Potter, Lisa H Butterfield

Open access · greenAbstract read
In one paragraph

Article in Journal of immunotherapy (Hagerstown, Md. : 1997). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

26 citing papers in PubMed, 54 citations in OpenAlex.

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  8. Cancer biomarkers for targeted therapy.Biomarker research · 2019
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  13. Lessons learned from cancer vaccine trials and target antigen choice.Cancer immunology, immunotherapy : CII · 2016
    Review
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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

4 authors at 2 institutions in 1 country.

Viktoria N EvdokimovaDepartment of Medicine, Division of Hematology/Oncology , University of Pittsburgh Cancer Institute, Pittsburgh, PA 15213, USA.
Yang Liu
Douglas M Potter
Lisa H Butterfield
Cancer Research And Biostatistics · USUPMC Hillman Cancer Center · US

Funding

AFP-BASED PRIME-BOOST IMMUNOTHERAPY OF HCCR01CA104524 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BUTTERFIELD, LISA HELENE · 2004 to 2006
$898k
NCI NIH HHS R01 CA104524
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is one of the most common cancers worldwide, and is often diagnosed at an advanced stage. We have investigated alpha-fetoprotein (AFP) as a tumor-associated antigen for HCC. We identified major histocompatibility complex class I-restricted peptide epitopes derived from AFP and studied CD8 T-cell responses in vivo and in vitro in ongoing immunotherapy studies. Helper T cells are of critical importance in shaping the immune response; therefore, we investigated the frequency and function of AFP-specific CD4 T cells in the general population and among HCC patients. CD4 T-cell responses were assessed by direct ex vivo multicytokine enzyme-linked immunospot assay and by measurement of cytokine levels using a multicytokine assay. Our analysis indicates that healthy donors have very low frequencies of AFP-specific CD4 T-cell responses, which are of TH1 type, detectable ex vivo. In contrast, these T cells were either reduced or eliminated in HCC patients at advanced stages of disease. To better activate these cells, we compared the stimulatory capacity of both AFP protein-fed and AdVhAFP-engineered dendritic cells (DC). Healthy donors have CD4 T-cell responses, which were activated in response to AFP protein-fed DC whereas HCC patients do not demonstrate significant responses to AFP protein. AdVhAFP-transduced DC were capable of activating higher frequency TH1 CD4 responses to AFP in both healthy donors and AFP-positive HCC patients. Importantly, CD4 T-cell cytokine expression profiles were skewed towards interleukin-2 and interferon-gamma production when activated by adenovirally engineered DC, which has therapeutic implications for vaccination efforts.

Indexed as

Gene Expression Regulation, Neoplasticalpha-FetoproteinsCarcinoma, HepatocellularCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCytokinesDendritic CellsFemaleHumansLeukocytes, MononuclearLiver NeoplasmsLymphocyte ActivationMalePeptidesT-Lymphocytes, Helper-Induceralpha-FetoproteinsCytokinesPeptides

Identifiers

PMID17457217
PMCPMC3612834
OpenAlexW2002223432

What OpenQuestion holds

Textmetadata
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.