Evidence map›Paper›PMID 19414747›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

Lentivector immunization stimulates potent CD8 T cell responses against melanoma self-antigen tyrosinase-related protein 1 and generates antitumor immunity in mice.

Yanjun Liu, Yibing Peng, Michael Mi, Jose Guevara-Patino, David H Munn, Ning Fu, Yukai He

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

28 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  6. Engineering T cells for immunotherapy of primary human hepatocellular carcinoma.Journal of genetics and genomics = Yi chuan xue bao · 2020
    Review
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors at 5 institutions in 2 countries.

Yanjun LiuImmunology/Immunotherapy Program, Medical College of Georgia Cancer Center, Medical College of Georgia, Augusta, GA 30912, USA.
Yibing Peng
Michael Mi
Jose Guevara-Patino
David H Munn
Ning Fu
Yukai He
Parker Institute for Cancer Immunotherapy · USAugusta University · USHarvard University · USLoyola University Chicago · USSouthern Medical University · CN

Funding

Mechanism of Eliciting Antitumor Cell Immunity Via Lentivector ImmunizationR01CA116444 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HE, YUKAI · 2007 to 2011
$1.4M
NCI NIH HHS R01 CA116444NCI NIH HHS R01CA16444
6 · The paper itself

Abstract

Recombinant lentivector immunization has been demonstrated to induce potent CD8 T cell responses in vivo. In this study, we investigated whether lentivector delivering a self/tumor Ag, tyrosinase related protein 1 (TRP1), could stimulate effective antitumor T cell responses. We found that immunization with lentivector expressing mutated TRP1 Ag elicited potent CD8 T cell responses against multiple TRP1 epitopes. Importantly, the activated CD8 T cells effectively recognize wild-type TRP1 epitopes. At peak times, as many as 10% of CD8 T cells were effector cells against TRP1 Ag. These cells killed wild-type TRP1 peptide-pulsed target cells in vivo and produced IFN-gamma after ex vivo stimulation. The CD8 T cell responses were long-lasting (3-4 wk). Immunized mice were protected from B16 tumor cell challenge. In a therapeutic setting, lentivector immunization induced potent CD8 T cell responses in tumor bearing mice. The number of infiltrating T cells and the ratio of CD8/CD4 were dramatically increased in the tumors of immunized mice. The tumor-infiltrating CD8 T cells were functional and produced IFN-gamma. The potent CD8 T cell responses stimulated by lentivector immunization eliminated small 3-day s.c. B16 tumors and strongly inhibited the growth of more established 5-day tumors. These studies demonstrate that genetic immunization with lentivector expressing mutated self/tumor Ag can generate potent CD8 T cell immune responses and antitumor immunity that prevent and inhibit B16 tumor growth, suggesting that lentivector immunization has the potential for tumor immunotherapy and immune prevention.

Indexed as

AnimalsAntigens, NeoplasmAutoantigensCancer VaccinesCD8-Positive T-LymphocytesEpitopes, T-LymphocyteFlow CytometryFluorescent Antibody TechniqueGenetic VectorsLentivirusLymphocytes, Tumor-InfiltratingMelanoma, ExperimentalMembrane GlycoproteinsMiceMutationOxidoreductasesAntigens, NeoplasmAutoantigensCancer VaccinesEpitopes, T-LymphocyteMembrane GlycoproteinsOxidoreductasesTyrp1 protein, mouse

Identifiers

PMID19414747
PMCPMC3077746
OpenAlexW2113779492

What OpenQuestion holds

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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.