Evidence map›Paper›PMID 24476798›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2014

Fusion of HCV nonstructural antigen to MHC class II-associated invariant chain enhances T-cell responses induced by vectored vaccines in nonhuman primates.

Stefania Capone, Mariarosaria Naddeo, Anna Morena D'Alise, Adele Abbate, Fabiana Grazioli, Annunziata Del Gaudio, Mariarosaria Del Sorbo, Maria Luisa Esposito, Virginia Ammendola, Gemma Perretta and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

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  8. Design and Immunological Validation ofFrontiers in immunology · 2021
    Article
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  15. Hepatitis C Vaccines, Antibodies, and T Cells.Frontiers in immunology · 2018
    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

15 authors at 3 institutions in 1 country.

Stefania CaponeOkairos, Rome, Italy.
Mariarosaria NaddeoOkairos, Rome, Italy.
Anna Morena D'AliseOkairos, Rome, Italy.
Adele AbbateOkairos, Rome, Italy.
Fabiana GrazioliOkairos, Rome, Italy.
Annunziata Del GaudioOkairos, Rome, Italy.
Mariarosaria Del SorboOkairos, Rome, Italy.
Maria Luisa EspositoOkairos, Rome, Italy.
Virginia AmmendolaOkairos, Rome, Italy.
Gemma PerrettaCellular Biology and Neurobiology Institute (IBCN) National Research Council of Italy, Rome, Italy.
Alessandra TaglioniCellular Biology and Neurobiology Institute (IBCN) National Research Council of Italy, Rome, Italy.
Stefano CollocaOkairos, Rome, Italy.
Alfredo Nicosia1] Okairos, Rome, Italy [2] CEINGE, Naples, Italy [3] Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy.
Riccardo Cortese1] Okairos, Rome, Italy [2] Okairos AG, c/o OBC Suisse AG, Basel, Switzerland.
Antonella FolgoriOkairos, Rome, Italy.
Institute of Cell Biology and Neurobiology · ITNational Research Council · ITUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite viral vectors being potent inducers of antigen-specific T cells, strategies to further improve their immunogenicity are actively pursued. Of the numerous approaches investigated, fusion of the encoded antigen to major histocompatibility complex class II-associated invariant chain (Ii) has been reported to enhance CD8(+) T-cell responses. We have previously shown that adenovirus vaccine encoding nonstructural (NS) hepatitis C virus (HCV) proteins induces potent T-cell responses in humans. However, even higher T-cell responses might be required to achieve efficacy against different HCV genotypes or therapeutic effect in chronically infected HCV patients. In this study, we assessed fusion of the HCV NS antigen to murine and human Ii expressed by the chimpanzee adenovirus vector ChAd3 or recombinant modified vaccinia Ankara in mice and nonhuman primates (NHPs). A dramatic increase was observed in outbred mice in which vaccination with ChAd3 expressing the fusion antigen resulted in a 10-fold increase in interferon-γ(+) CD8(+) T cells. In NHPs, CD8(+) T-cell responses were enhanced and accelerated with vectors encoding the Ii-fused antigen. These data show for the first time that the enhancement induced by vector vaccines encoding li-fused antigen was not species specific and can be translated from mice to NHPs, opening the way for testing in humans.

Indexed as

AdenoviridaeAnimalsAntigens, Differentiation, B-LymphocyteAntigens, ViralCD8-Positive T-LymphocytesGenes, MHC Class IIHepacivirusHepatitis CHistocompatibility Antigens Class IIHumansInterferon-gammaMicePan troglodytesRecombinant Fusion ProteinsVaccinesAntigens, Differentiation, B-LymphocyteAntigens, ViralHistocompatibility Antigens Class IIInterferon-gammainvariant chainRecombinant Fusion ProteinsVaccines

Identifiers

PMID24476798
PMCPMC4015230
OpenAlexW2014920221

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.